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    <title>Recent nobel_j2009_blackburn items</title>
    <link>https://escholarship.org/uc/nobel_j2009_blackburn/rss</link>
    <description>Recent eScholarship items from Elizabeth Blackburn, UCSF (Nobel Prize in Physiology or Medicine, 2009)</description>
    <pubDate>Sun, 20 Sep 2026 22:41:16 +0000</pubDate>
    <item>
      <title>Seasonal variation of peripheral blood leukocyte telomere length in Costa Rica: A population‐based observational study</title>
      <link>https://escholarship.org/uc/item/91t423xn</link>
      <description>OBJECTIVES: Peripheral blood leukocyte telomere length (LTL) is increasingly being used as a biomarker of aging, but its natural variation in human populations is not well understood. Several other biomarkers show seasonal variation, as do several determinants of LTL. We examined whether there was monthly variation in LTL in Costa Rica, a country with strong seasonal differences in precipitation and infection.
METHODS: We examined a longitudinal population-based cohort of 581 Costa Rican adults age 60 and above, from which blood samples were drawn between October 2006 and July 2008. LTL was assayed from these samples using the quantitative PCR method. Multivariate regression models were used to examine correlations between month of blood draw and LTL.
RESULTS: Telomere length from peripheral blood leukocytes varied by as much as 200 base pairs depending on month of blood draw, and this difference is not likely to be due to random variation. A moderate proportion of this association...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/91t423xn</guid>
      <pubDate>Mon, 17 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Rehkopf, David H</name>
      </author>
      <author>
        <name>Dow, William H</name>
        <uri>https://orcid.org/0000-0002-4080-1668</uri>
      </author>
      <author>
        <name>Rosero‐Bixby, Luis</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
    </item>
    <item>
      <title>Leukocyte Telomere Length and Mortality in the National Health and Nutrition Examination Survey, 1999–2002</title>
      <link>https://escholarship.org/uc/item/3933b016</link>
      <description>BACKGROUND: This study examined the association between leukocyte telomere length--a marker of cell aging--and mortality in a nationally representative sample of US adults ages 50-84 years. We also examined moderating effects of age, sex, race/ethnicity, and education.
METHODS: Data were from the National Health and Nutrition Examination Survey, 1999-2002 (n = 3,091). Cox proportional hazards regression was used to estimate the risk of all-cause and cause- specific mortality adjusting for sociodemographic characteristics, smoking, body mass index, and chronic conditions.
RESULTS: Eight hundred and seventy deaths occurred over an average of 9.5 years of follow-up. In the full sample, a decrease of 1 kilobase pair in telomere length at baseline was marginally associated with a 10% increased hazard of all-cause mortality (hazard ratio [HR]: 1.1, 95% confidence interval [CI]: 0.9, 1.4) and a 30% increased hazard of death due to diseases other than cardiovascular disease or cancer...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3933b016</guid>
      <pubDate>Mon, 17 Apr 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Needham, Belinda L</name>
      </author>
      <author>
        <name>Rehkopf, David</name>
      </author>
      <author>
        <name>Adler, Nancy</name>
      </author>
      <author>
        <name>Gregorich, Steven</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
    </item>
    <item>
      <title>Psychiatric disorders and leukocyte telomere length: Underlying mechanisms linking mental illness with cellular aging</title>
      <link>https://escholarship.org/uc/item/2t48960r</link>
      <description>Many psychiatric illnesses are associated with early mortality and with an increased risk of developing physical diseases that are more typically seen in the elderly. Moreover, certain psychiatric illnesses may be associated with accelerated cellular aging, evidenced by shortened leukocyte telomere length (LTL), which could underlie this association. Shortened LTL reflects a cell's mitotic history and cumulative exposure to inflammation and oxidation as well as the availability of telomerase, a telomere-lengthening enzyme. Critically short telomeres can cause cells to undergo senescence, apoptosis or genomic instability, and shorter LTL correlates with poorer health and predicts mortality. Emerging data suggest that LTL may be reduced in certain psychiatric illnesses, perhaps in proportion to exposure to the psychiatric illnesses, although conflicting data exist. Telomerase has been less well characterized in psychiatric illnesses, but a role in depression and in antidepressant...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2t48960r</guid>
      <pubDate>Mon, 17 Apr 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Lindqvist, Daniel</name>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
      <author>
        <name>Mellon, Synthia H</name>
      </author>
      <author>
        <name>Penninx, Brenda W</name>
      </author>
      <author>
        <name>Révész, Dóra</name>
      </author>
      <author>
        <name>Verhoeven, Josine E</name>
      </author>
      <author>
        <name>Reus, Victor I</name>
        <uri>https://orcid.org/0000-0002-8193-5697</uri>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Mahan, Laura</name>
      </author>
      <author>
        <name>Hough, Christina M</name>
        <uri>https://orcid.org/0000-0002-8864-5262</uri>
      </author>
      <author>
        <name>Rosser, Rebecca</name>
      </author>
      <author>
        <name>Bersani, F Saverio</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Wolkowitz, Owen M</name>
        <uri>https://orcid.org/0000-0003-0655-5042</uri>
      </author>
    </item>
    <item>
      <title>PBMC telomerase activity, but not leukocyte telomere length, correlates with hippocampal volume in major depression</title>
      <link>https://escholarship.org/uc/item/0ff5p6w1</link>
      <description>Accelerated cell aging, indexed in peripheral leukocytes by telomere shortness and in peripheral blood mononuclear cells (PBMCs) by telomerase activity, has been reported in several studies of major depressive disorder (MDD). However, the relevance of these peripheral measures for brain indices that are presumably more directly related to MDD pathophysiology is unknown. In this study, we explored the relationship between PBMC telomerase activity and leukocyte telomere length and magnetic resonance imaging-estimated hippocampal volume in un-medicated depressed individuals and healthy controls. We predicted that, to the extent peripheral and central telomerase activity are directly related, PBMC telomerase activity would be positively correlated with hippocampal volume, perhaps due to hippocampal telomerase-associated neurogenesis, neuroprotection or neurotrophic facilitation, and that this effect would be clearer in individuals with increased PBMC telomerase activity, as previously...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0ff5p6w1</guid>
      <pubDate>Sun, 16 Apr 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Wolkowitz, Owen M</name>
        <uri>https://orcid.org/0000-0003-0655-5042</uri>
      </author>
      <author>
        <name>Mellon, Synthia H</name>
      </author>
      <author>
        <name>Lindqvist, Daniel</name>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Reus, Victor I</name>
        <uri>https://orcid.org/0000-0002-8193-5697</uri>
      </author>
      <author>
        <name>Burke, Heather</name>
      </author>
      <author>
        <name>Rosser, Rebecca</name>
      </author>
      <author>
        <name>Mahan, Laura</name>
      </author>
      <author>
        <name>Mackin, Scott</name>
      </author>
      <author>
        <name>Yang, Tony</name>
      </author>
      <author>
        <name>Weiner, Michael</name>
      </author>
      <author>
        <name>Mueller, Susanne</name>
      </author>
    </item>
    <item>
      <title>Telomere Length and the Risk of Atrial Fibrillation</title>
      <link>https://escholarship.org/uc/item/603207x5</link>
      <description>BACKGROUND: Advanced age is the most important risk factor for atrial fibrillation (AF); however, the mechanism remains unknown. Telomeres, regions of DNA that shorten with cell division, are considered reliable markers of biological aging. We sought to examine the association between leukocyte telomere length (LTL) and incident AF in a large population-based cohort using direct LTL measurements and genetic data. To further explore our findings, we compared atrial cell telomere length and LTL in cardiac surgery patients.
METHODS AND RESULTS: Mean LTL and the TERT rs2736100 single nucleotide polymorphism were assessed as predictors of incident AF in the Cardiovascular Health Study (CHS). Among the surgical patients, within subject comparison of atrial cell telomere length versus LTL was assessed. Among 1639 CHS participants, we observed no relationship between mean LTL and incident AF before and after adjustment for potential confounders (adjusted hazard ratio, 1.09; 95% confidence...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/603207x5</guid>
      <pubDate>Fri, 14 Apr 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Roberts, Jason D</name>
      </author>
      <author>
        <name>Dewland, Thomas A</name>
      </author>
      <author>
        <name>Longoria, James</name>
      </author>
      <author>
        <name>Fitzpatrick, Annette L</name>
      </author>
      <author>
        <name>Ziv, Elad</name>
      </author>
      <author>
        <name>Hu, Donglei</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Glidden, David V</name>
        <uri>https://orcid.org/0000-0001-5888-1419</uri>
      </author>
      <author>
        <name>Psaty, Bruce M</name>
      </author>
      <author>
        <name>Burchard, Esteban G</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Olgin, Jeffrey E</name>
      </author>
      <author>
        <name>Heckbert, Susan R</name>
      </author>
      <author>
        <name>Marcus, Gregory M</name>
        <uri>https://orcid.org/0000-0001-5197-7696</uri>
      </author>
    </item>
    <item>
      <title>Associations of Cadmium and Lead Exposure With Leukocyte Telomere Length: Findings From National Health and Nutrition Examination Survey, 1999–2002</title>
      <link>https://escholarship.org/uc/item/40k2g2z8</link>
      <description>Cadmium and lead are ubiquitous environmental contaminants that might increase risks of cardiovascular disease and other aging-related diseases, but their relationships with leukocyte telomere length (LTL), a marker of cellular aging, are poorly understood. In experimental studies, they have been shown to induce telomere shortening, but no epidemiologic study to date has examined their associations with LTL in the general population. We examined associations of blood lead and cadmium (n = 6,796) and urine cadmium (n = 2,093) levels with LTL among a nationally representative sample of US adults from the National Health and Nutrition Examination Survey (1999-2002). The study population geometric mean concentrations were 1.67 µg/dL (95% confidence interval (CI): 1.63, 1.70) for blood lead, 0.44 µg/L (95% CI: 0.42, 0.47) for blood cadmium, and 0.28 µg/L (95% CI: 0.27, 0.30) for urine cadmium. After adjustment for potential confounders, the highest (versus lowest) quartiles of blood...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/40k2g2z8</guid>
      <pubDate>Fri, 14 Apr 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Zota, Ami R</name>
      </author>
      <author>
        <name>Needham, Belinda L</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Park, Sung Kyun</name>
      </author>
      <author>
        <name>Rehkopf, David H</name>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
    </item>
    <item>
      <title>Soda and Cell Aging: Associations between Sugar-Sweetened Beverage Consumption and Leukocyte Telomere Length in Healthy Adults from the National Health and Nutrition Examination Surveys</title>
      <link>https://escholarship.org/uc/item/2fw7k79g</link>
      <description>OBJECTIVES: We tested whether leukocyte telomere length maintenance, which underlies healthy cellular aging, provides a link between sugar-sweetened beverage (SSB) consumption and the risk of cardiometabolic disease.
METHODS: We examined cross-sectional associations between the consumption of SSBs, diet soda, and fruit juice and telomere length in a nationally representative sample of healthy adults. The study population included 5309 US adults, aged 20 to 65 years, with no history of diabetes or cardiovascular disease, from the 1999 to 2002 National Health and Nutrition Examination Surveys. Leukocyte telomere length was assayed from DNA specimens. Diet was assessed using 24-hour dietary recalls. Associations were examined using multivariate linear regression for the outcome of log-transformed telomere length.
RESULTS: After adjustment for sociodemographic and health-related characteristics, sugar-sweetened soda consumption was associated with shorter telomeres (b = -0.010; 95%...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2fw7k79g</guid>
      <pubDate>Fri, 14 Apr 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Leung, Cindy W</name>
      </author>
      <author>
        <name>Laraia, Barbara A</name>
        <uri>https://orcid.org/0000-0002-0493-2900</uri>
      </author>
      <author>
        <name>Needham, Belinda L</name>
      </author>
      <author>
        <name>Rehkopf, David H</name>
      </author>
      <author>
        <name>Adler, Nancy E</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
    </item>
    <item>
      <title>Adverse childhood experiences and leukocyte telomere maintenance in depressed and healthy adults</title>
      <link>https://escholarship.org/uc/item/9r4572ct</link>
      <description>BACKGROUND: Adverse childhood experiences (ACEs) are associated with poor physical and mental health outcomes in adulthood. Adverse childhood experiences are also associated with shortened leukocyte telomere length (LTL) in adults, suggesting accelerated cell aging. No studies have yet assessed the relationship of ACEs to LTL in individuals with major depressive disorder (MDD), despite the high incidence of antecedent ACEs in individuals with MDD. Further, no studies in any population have assessed the relationship of ACEs to the activity of telomerase, the major enzyme responsible for maintaining LTL, or the relationship between telomerase and LTL in individuals with ACEs.
METHODS: Twenty healthy, unmedicated adults with MDD and 20 healthy age-, sex- and ethnicity-matched controls had ACEs assessed and had blood drawn for LTL and peripheral blood mononuclear cell (PBMC) resting telomerase activity.
RESULTS: In healthy controls, greater ACE exposure was associated with shorter...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9r4572ct</guid>
      <pubDate>Tue, 11 Apr 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Chen, Stephen H</name>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
      <author>
        <name>Mellon, Synthia H</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Reus, Victor I</name>
        <uri>https://orcid.org/0000-0002-8193-5697</uri>
      </author>
      <author>
        <name>Rosser, Rebecca</name>
      </author>
      <author>
        <name>Kupferman, Eve</name>
      </author>
      <author>
        <name>Burke, Heather</name>
      </author>
      <author>
        <name>Mahan, Laura</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Wolkowitz, Owen M</name>
        <uri>https://orcid.org/0000-0003-0655-5042</uri>
      </author>
    </item>
    <item>
      <title>Multisystem resiliency moderates the major depression–Telomere length association: Findings from the Heart and Soul Study</title>
      <link>https://escholarship.org/uc/item/86c88120</link>
      <description>Major depressive disorder (MDD) has been associated with reduced leukocyte telomere length (LTL). It is not known, however, whether psychosocial and behavioral protective factors moderate this association. In the current study, we examine whether multisystem resiliency--defined by healthy emotion regulation, strong social connections, and health behaviors (sleep and exercise)--predicts LTL and mitigates previously demonstrated associations between depression diagnosis and LTL. LTL was measured, using a quantitative PCR assay, in 954 patients with stable cardiovascular disease in the Heart and Soul Study. In a fully adjusted model, high multisystem resiliency predicted longer LTL (b=80.00, SE=27.17, p=.003), whereas each individual factor did not. Multisystem resiliency significantly moderated the MDD-LTL association (p=.02). Specifically, MDD was significantly related to LTL at 1 SD below the mean of multisystem resiliency (b=-142.86, SE=56.46, p=.01), but not at 1 SD above the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/86c88120</guid>
      <pubDate>Sat, 1 Apr 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Puterman, Eli</name>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Gross, James J</name>
      </author>
      <author>
        <name>Whooley, Mary A</name>
      </author>
      <author>
        <name>Cohen, Beth E</name>
      </author>
    </item>
    <item>
      <title>Socioeconomic status, health behavior, and leukocyte telomere length in the National Health and Nutrition Examination Survey, 1999–2002</title>
      <link>https://escholarship.org/uc/item/3t62z2cs</link>
      <description>The purpose of this study was to examine the association between socioeconomic status (SES) and leukocyte telomere length (LTL) - a marker of cell aging that has been linked to stressful life circumstances - in a nationally representative, socioeconomically and ethnically diverse sample of US adults aged 20-84. Using data from the National Health and Nutrition Examination Survey (NHANES), 1999-2002, we found that respondents who completed less than a high school education had significantly shorter telomeres than those who graduated from college. Income was not associated with LTL. African-Americans had significantly longer telomeres than whites, but there were no significant racial/ethnic differences in the association between education and telomere length. Finally, we found that the association between education and LTL was partially mediated by smoking and body mass index but not by drinking or sedentary behavior.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3t62z2cs</guid>
      <pubDate>Sat, 1 Apr 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Needham, Belinda L</name>
      </author>
      <author>
        <name>Adler, Nancy</name>
      </author>
      <author>
        <name>Gregorich, Steven</name>
      </author>
      <author>
        <name>Rehkopf, David</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
    </item>
    <item>
      <title>Dynamic Imaging of Genomic Loci in Living Human Cells by an Optimized CRISPR/Cas System</title>
      <link>https://escholarship.org/uc/item/4bn9n81z</link>
      <description>The spatiotemporal organization and dynamics of chromatin play critical roles in regulating genome function. However, visualizing specific, endogenous genomic loci remains challenging in living cells. Here, we demonstrate such an imaging technique by repurposing the bacterial CRISPR/Cas system.&amp;nbsp;Using an EGFP-tagged endonuclease-deficient Cas9 protein and a structurally optimized small guide (sg) RNA, we show robust imaging of repetitive elements in telomeres and coding genes in living cells. Furthermore, an array of sgRNAs tiling along the target locus enables the visualization of nonrepetitive genomic sequences. Using this method, we have studied telomere dynamics during elongation or disruption, the subnuclear localization of the MUC4 loci, the cohesion of replicated MUC4 loci on sister chromatids, and their dynamic behaviors during mitosis. This CRISPR imaging tool has potential to significantly improve the capacity to study the conformation and dynamics of native chromosomes...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4bn9n81z</guid>
      <pubDate>Fri, 27 Jan 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Chen, Baohui</name>
      </author>
      <author>
        <name>Gilbert, Luke A</name>
      </author>
      <author>
        <name>Cimini, Beth A</name>
      </author>
      <author>
        <name>Schnitzbauer, Joerg</name>
      </author>
      <author>
        <name>Zhang, Wei</name>
      </author>
      <author>
        <name>Li, Gene-Wei</name>
      </author>
      <author>
        <name>Park, Jason</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Weissman, Jonathan S</name>
      </author>
      <author>
        <name>Qi, Lei S</name>
      </author>
      <author>
        <name>Huang, Bo</name>
      </author>
    </item>
    <item>
      <title>Unprecedented Opportunities and Promise for Cancer Prevention Research</title>
      <link>https://escholarship.org/uc/item/8jm2k8d9</link>
      <description>Cancer prevention encompasses a wide range of highly developed science and clinical impact. Enunciating these two aspects in the same breath highlights the crucial link between them. The breadth and excitement of current opportunities in the science of cancer prevention have never been greater. Major avenues of such research include the extent and effect of premalignancy, the molecular underpinnings of carcinogenesis and related prevention targets, in vitro model systems of the progression of normal human epithelial cells to tumorigenesis, molecular risk stratification and pharmacogenomic approaches, and many more. We describe the clinical impacts of cancer prevention (with examples in the areas of molecular targeting, vaccines, epidemiology, and behavioral science) and the stage-setting science that facilitated them. In addition, discussed are new prevention opportunities such as interactions between stromal and microenvironmental factors, the control of premalignant stem cell...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8jm2k8d9</guid>
      <pubDate>Fri, 18 Feb 2022 00:00:00 +0000</pubDate>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Tlsty, Thea D</name>
        <uri>https://orcid.org/0000-0003-0903-1631</uri>
      </author>
      <author>
        <name>Lippman, Scott M</name>
      </author>
    </item>
    <item>
      <title>Human Rif1 protein binds aberrant telomeres and aligns along anaphase midzone microtubules</title>
      <link>https://escholarship.org/uc/item/5rm9v53n</link>
      <description>We identified and characterized a human orthologue of Rif1 protein, which in budding yeast interacts in vivo with the major duplex telomeric DNA binding protein Rap1p and negatively regulates telomere length. Depletion of hRif1 by RNA interference in human cancer cells impaired cell growth but had no detectable effect on telomere length, although hRif1 overexpression in S. cerevisiae interfered with telomere length control, in a manner specifically dependent on the presence of yeast Rif1p. No localization of hRif1 on normal human telomeres, or interaction with the human telomeric proteins TRF1, TRF2, or hRap1, was detectable. However, hRif1 efficiently translocated to telomerically located DNA damage foci in response to the synthesis of aberrant telomeres directed by mutant-template telomerase RNA. The hRif1 level rose during late S/G2 but hRif1 was not visible on chromosomes in metaphase and anaphase; however, notably, specifically during early anaphase, hRif1 aligned along a...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5rm9v53n</guid>
      <pubDate>Tue, 19 May 2020 00:00:00 +0000</pubDate>
      <author>
        <name>Xu, Lifeng</name>
        <uri>https://orcid.org/0000-0002-7887-5451</uri>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
    </item>
    <item>
      <title>Rapid telomere motions in live human cells analyzed by highly time-resolved microscopy</title>
      <link>https://escholarship.org/uc/item/9f40r6r6</link>
      <description>BackgroundTelomeres cap chromosome ends and protect the genome. We studied individual telomeres in live human cancer cells. In capturing telomere motions using quantitative imaging to acquire complete high-resolution three-dimensional datasets every second for 200 seconds, telomere dynamics were systematically analyzed.ResultsThe motility of individual telomeres within the same cancer cell nucleus was widely heterogeneous. One class of internal heterochromatic regions of chromosomes analyzed moved more uniformly and showed less motion and heterogeneity than telomeres. The single telomere analyses in cancer cells revealed that shorter telomeres showed more motion, and the more rapid telomere motions were energy dependent. Experimentally increasing bulk telomere length dampened telomere motion. In contrast, telomere uncapping, but not a DNA damaging agent, methyl methanesulfonate, significantly increased telomere motion.ConclusionNew methods for seconds-scale, four-dimensional,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9f40r6r6</guid>
      <pubDate>Sun, 17 May 2020 00:00:00 +0000</pubDate>
      <author>
        <name>Wang, Xueying</name>
      </author>
      <author>
        <name>Kam, Zvi</name>
      </author>
      <author>
        <name>Carlton, Peter M</name>
      </author>
      <author>
        <name>Xu, Lifeng</name>
        <uri>https://orcid.org/0000-0002-7887-5451</uri>
      </author>
      <author>
        <name>Sedat, John W</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
    </item>
    <item>
      <title>A Common Variant in the Telomerase RNA Component Is Associated with Short Telomere Length</title>
      <link>https://escholarship.org/uc/item/8zh627h9</link>
      <description>BACKGROUND: Telomeres shorten as cells divide. This shortening is compensated by the enzyme telomerase. We evaluated the effect of common variants in the telomerase RNA component (TERC) gene on telomere length (TL) in the population-based Health Aging and Body Composition (Health ABC) Study and in two replication samples (the TwinsUK Study and the Amish Family Osteoporosis Study, AFOS).
METHODOLOGY: Five variants were identified in the TERC region by sequence analysis and only one SNP was common (rs2293607, G/A). The frequency of the G allele was 0.26 and 0.07 in white and black, respectively. Testing for association between TL and rs2293607 was performed using linear regression models or variance component analysis conditioning on relatedness among subjects.
RESULTS: The adjusted mean TL was significantly shorter in 665 white carriers of the G allele compared to 887 non-carriers from the Health ABC Study (4.69±0.05 kbp vs. 4.86±0.04 kbp, measured by quantitative PCR, p = 0.005)....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8zh627h9</guid>
      <pubDate>Sun, 17 May 2020 00:00:00 +0000</pubDate>
      <author>
        <name>Njajou, Omer T</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Pawlikowska, Ludmila</name>
      </author>
      <author>
        <name>Mangino, Massimo</name>
      </author>
      <author>
        <name>Damcott, Coleen M</name>
      </author>
      <author>
        <name>Kwok, Pui-Yan</name>
        <uri>https://orcid.org/0000-0002-5087-3059</uri>
      </author>
      <author>
        <name>Spector, Timothy D</name>
      </author>
      <author>
        <name>Newman, Anne B</name>
      </author>
      <author>
        <name>Harris, Tamara B</name>
      </author>
      <author>
        <name>Cummings, Steven R</name>
      </author>
      <author>
        <name>Cawthon, Richard M</name>
      </author>
      <author>
        <name>Shuldiner, Alan R</name>
      </author>
      <author>
        <name>Valdes, Ana M</name>
      </author>
      <author>
        <name>Hsueh, Wen-Chi</name>
      </author>
    </item>
    <item>
      <title>Leukocyte Telomere Length in Major Depression: Correlations with Chronicity, Inflammation and Oxidative Stress - Preliminary Findings</title>
      <link>https://escholarship.org/uc/item/7vn8j5dk</link>
      <description>BACKGROUND: Depression is associated with an unusually high rate of aging-related illnesses and early mortality. One aspect of "accelerated aging" in depression may be shortened leukocyte telomeres. When telomeres critically shorten, as often occurs with repeated mitoses or in response to oxidation and inflammation, cells may die. Indeed, leukocyte telomere shortening predicts early mortality and medical illnesses in non-depressed populations. We sought to determine if leukocyte telomeres are shortened in Major Depressive Disorder (MDD), whether this is a function of lifetime depression exposure and whether this is related to putative mediators, oxidation and inflammation.
METHODOLOGY: Leukocyte telomere length was compared between 18 unmedicated MDD subjects and 17 controls and was correlated with lifetime depression chronicity and peripheral markers of oxidation (F2-isoprostane/Vitamin C ratio) and inflammation (IL-6). Analyses were controlled for age and sex.
PRINCIPAL FINDINGS:...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7vn8j5dk</guid>
      <pubDate>Sun, 17 May 2020 00:00:00 +0000</pubDate>
      <author>
        <name>Wolkowitz, Owen M</name>
        <uri>https://orcid.org/0000-0003-0655-5042</uri>
      </author>
      <author>
        <name>Mellon, Synthia H</name>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Dhabhar, Firdaus S</name>
      </author>
      <author>
        <name>Su, Yali</name>
      </author>
      <author>
        <name>Reus, Victor I</name>
        <uri>https://orcid.org/0000-0002-8193-5697</uri>
      </author>
      <author>
        <name>Rosser, Rebecca</name>
      </author>
      <author>
        <name>Burke, Heather M</name>
      </author>
      <author>
        <name>Kupferman, Eve</name>
      </author>
      <author>
        <name>Compagnone, Mariana</name>
      </author>
      <author>
        <name>Nelson, J Craig</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
    </item>
    <item>
      <title>Impartial comparative analysis of measurement of leukocyte telomere length/DNA content by Southern blots and qPCR</title>
      <link>https://escholarship.org/uc/item/3rg1v2gm</link>
      <description>Telomere length/DNA content has been measured in epidemiological/clinical settings with the goal of testing a host of hypotheses related to the biology of human aging, but often the conclusions of these studies have been inconsistent. These inconsistencies may stem from various reasons, including the use of different telomere length measurement techniques. Here, we report the first impartial evaluation of measurements of leukocyte telomere length by Southern blot of the terminal restriction fragments and quantitative PCR (qPCR) of telomere DNA content, expressed as the ratio of telomeric product (T)/single copy gene (S) product. Blind measurements on the same samples from 50 donors were performed in two independent laboratories on two different occasions. Both the qPCR and Southern blots displayed highly reproducible results as shown by r values &amp;gt; 0.9 for the correlations between results obtained by either method on two occasions. The inter-assay CV measurement for the qPCR...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3rg1v2gm</guid>
      <pubDate>Sun, 17 May 2020 00:00:00 +0000</pubDate>
      <author>
        <name>Aviv, Abraham</name>
      </author>
      <author>
        <name>Hunt, Steven C</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Cao, Xiaojian</name>
      </author>
      <author>
        <name>Kimura, Masayuki</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth</name>
      </author>
    </item>
    <item>
      <title>Telomere Length Trajectory and Its Determinants in Persons with Coronary Artery Disease: Longitudinal Findings from the Heart and Soul Study</title>
      <link>https://escholarship.org/uc/item/22d5v28r</link>
      <description>BACKGROUND: Leukocyte telomere length, an emerging marker of biological age, has been shown to predict cardiovascular morbidity and mortality. However, the natural history of telomere length in patients with coronary artery disease has not been studied. We sought to investigate the longitudinal trajectory of telomere length, and to identify the independent predictors of telomere shortening, in persons with coronary artery disease.
METHODOLOGY/PRINCIPAL FINDINGS: In a prospective cohort study of 608 individuals with stable coronary artery disease, we measured leukocyte telomere length at baseline, and again after five years of follow-up. We used multivariable linear and logistic regression models to identify the independent predictors of leukocyte telomere trajectory. Baseline and follow-up telomere lengths were normally distributed. Mean telomere length decreased by 42 base pairs per year (p&amp;lt;0.001). Three distinct telomere trajectories were observed: shortening in 45%, maintenance...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/22d5v28r</guid>
      <pubDate>Sun, 17 May 2020 00:00:00 +0000</pubDate>
      <author>
        <name>Farzaneh-Far, Ramin</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Epel, Elissa</name>
      </author>
      <author>
        <name>Lapham, Kyle</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth</name>
      </author>
      <author>
        <name>Whooley, Mary A</name>
      </author>
    </item>
    <item>
      <title>The rate of leukocyte telomere shortening predicts mortality from cardiovascular disease in elderly men</title>
      <link>https://escholarship.org/uc/item/5z34g2st</link>
      <description>Telomere length (TL) has been proposed as a marker of mitotic cell age and as a general index of human organismic aging. Short absolute leukocyte telomere length has been linked to cardiovascular-related morbidity and mortality. Our aim was to test whether the rate of change in leukocyte TL is related to mortality in a healthy elderly cohort. We examined a subsample of 236 randomly selected Caucasian participants from the MacArthur Health Aging Study (aged 70 to 79 years). DNA samples from baseline and 2.5 years later were assayed for mean TL of leukocytes. Percent change in TL was calculated as a measure of TL change (TLC). Associations between TL and TLC with 12-year overall and cardiovascular mortality were assessed. Over the 2.5 year period, 46% of the study participants showed maintenance of mean bulk TL, whereas 30% showed telomere shortening, and, unexpectedly, 24% showed telomere lengthening. For women, short baseline TL was related to greater mortality from cardiovascular...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5z34g2st</guid>
      <pubDate>Sat, 16 May 2020 00:00:00 +0000</pubDate>
      <author>
        <name>Epel, Elissa S</name>
      </author>
      <author>
        <name>Merkin, Sharon Stein</name>
      </author>
      <author>
        <name>Cawthon, Richard</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Adler, Nancy E</name>
      </author>
      <author>
        <name>Pletcher, Mark J</name>
        <uri>https://orcid.org/0000-0002-6966-1312</uri>
      </author>
      <author>
        <name>Seeman, Teresa E</name>
      </author>
    </item>
    <item>
      <title>The Power of Exercise: Buffering the Effect of Chronic Stress on Telomere Length</title>
      <link>https://escholarship.org/uc/item/3061911b</link>
      <description>BACKGROUND: Chronic psychological stress is associated with detrimental effects on physical health, and may operate in part through accelerated cell aging, as indexed by shorter telomeres at the ends of chromosomes. However, not all people under stress have distinctly short telomeres, and we examined whether exercise can serve a stress-buffering function. We predicted that chronic stress would be related to short telomere length (TL) in sedentary individuals, whereas in those who exercise, stress would not have measurable effects on telomere shortening.
METHODOLOGY AND PRINCIPAL FINDINGS: 63 healthy post-menopausal women underwent a fasting morning blood draw for whole blood TL analysis by a quantitative polymerase chain reaction method. Participants completed the Perceived Stress Scale (Cohen et al., 1983), and for three successive days reported daily minutes of vigorous activity. Participants were categorized into two groups-sedentary and active (those getting Centers for Disease...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3061911b</guid>
      <pubDate>Sat, 16 May 2020 00:00:00 +0000</pubDate>
      <author>
        <name>Puterman, Eli</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Blackburn, Elizabeth</name>
      </author>
      <author>
        <name>O'Donovan, Aoife</name>
        <uri>https://orcid.org/0000-0003-2353-7217</uri>
      </author>
      <author>
        <name>Adler, Nancy</name>
      </author>
      <author>
        <name>Epel, Elissa</name>
      </author>
    </item>
    <item>
      <title>Changes in stress, eating, and metabolic factors are related to changes in telomerase activity in a randomized mindfulness intervention pilot study</title>
      <link>https://escholarship.org/uc/item/25g7r37j</link>
      <description>BACKGROUND: Psychological distress and metabolic dysregulation are associated with markers of accelerated cellular aging, including reduced telomerase activity and shortened telomere length. We examined whether participation in a mindfulness-based intervention, and, secondarily, improvements in psychological distress, eating behavior, and metabolic factors are associated with increases in telomerase activity in peripheral blood mononuclear cells (PBMCs).
METHODS: We enrolled 47 overweight/obese women in a randomized waitlist-controlled pilot trial (n=47) of a mindfulness-based intervention for stress eating and examined changes in telomerase activity from pre- to post-intervention. In secondary analyses, changes in telomerase activity across the sample were examined in relation to pre- to post-intervention changes in psychological distress, eating behavior, and metabolic factors (weight, serum cortisol, fasting glucose and insulin, and insulin resistance).
RESULTS: Both groups...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/25g7r37j</guid>
      <pubDate>Fri, 28 Jun 2019 00:00:00 +0000</pubDate>
      <author>
        <name>Daubenmier, Jennifer</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Blackburn, Elizabeth</name>
      </author>
      <author>
        <name>Hecht, Frederick M</name>
        <uri>https://orcid.org/0000-0002-5782-1171</uri>
      </author>
      <author>
        <name>Kristeller, Jean</name>
      </author>
      <author>
        <name>Maninger, Nicole</name>
      </author>
      <author>
        <name>Kuwata, Margaret</name>
      </author>
      <author>
        <name>Bacchetti, Peter</name>
        <uri>https://orcid.org/0000-0002-9323-2972</uri>
      </author>
      <author>
        <name>Havel, Peter J</name>
        <uri>https://orcid.org/0000-0003-3652-8301</uri>
      </author>
      <author>
        <name>Epel, Elissa</name>
      </author>
    </item>
    <item>
      <title>PBMC telomerase activity, but not leukocyte telomere length, correlates with hippocampal volume in major depression</title>
      <link>https://escholarship.org/uc/item/64d7t3m6</link>
      <description>Accelerated cell aging, indexed in peripheral leukocytes by telomere shortness and in peripheral blood mononuclear cells (PBMCs) by telomerase activity, has been reported in several studies of major depressive disorder (MDD). However, the relevance of these peripheral measures for brain indices that are presumably more directly related to MDD pathophysiology is unknown. In this study, we explored the relationship between PBMC telomerase activity and leukocyte telomere length and magnetic resonance imaging-estimated hippocampal volume in un-medicated depressed individuals and healthy controls. We predicted that, to the extent peripheral and central telomerase activity are directly related, PBMC telomerase activity would be positively correlated with hippocampal volume, perhaps due to hippocampal telomerase-associated neurogenesis, neuroprotection or neurotrophic facilitation, and that this effect would be clearer in individuals with increased PBMC telomerase activity, as previously...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/64d7t3m6</guid>
      <pubDate>Tue, 18 Sep 2018 00:00:00 +0000</pubDate>
      <author>
        <name>Wolkowitz, OM</name>
        <uri>https://orcid.org/0000-0003-0655-5042</uri>
      </author>
      <author>
        <name>Mellon, SH</name>
      </author>
      <author>
        <name>Lindqvist, D</name>
      </author>
      <author>
        <name>Epel, ES</name>
      </author>
      <author>
        <name>Blackburn, EH</name>
      </author>
      <author>
        <name>Lin, J</name>
      </author>
      <author>
        <name>Reus, VI</name>
        <uri>https://orcid.org/0000-0002-8193-5697</uri>
      </author>
      <author>
        <name>Burke, H</name>
      </author>
      <author>
        <name>Rosser, R</name>
      </author>
      <author>
        <name>Mahan, L</name>
      </author>
      <author>
        <name>Mackin, S</name>
      </author>
      <author>
        <name>Yang, T</name>
      </author>
      <author>
        <name>Weiner, M</name>
      </author>
      <author>
        <name>Mueller, S</name>
      </author>
    </item>
    <item>
      <title>Too toxic to ignore</title>
      <link>https://escholarship.org/uc/item/9g16z6kp</link>
      <description>Too toxic to ignore</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9g16z6kp</guid>
      <pubDate>Mon, 17 Sep 2018 00:00:00 +0000</pubDate>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
    </item>
    <item>
      <title>Mitochondrial DNA copy number is reduced in male combat veterans with PTSD</title>
      <link>https://escholarship.org/uc/item/1k0456d5</link>
      <description>INTRODUCTION: Mitochondrial abnormalities may be involved in PTSD, although few studies have examined this. Mitochondrial DNA copy number (mtDNAcn) in blood cells is an emerging systemic index of mitochondrial biogenesis and function. The present study assessed mtDNAcn in male combat-exposed veterans with PTSD compared to those without PTSD as well as its correlation with clinical scales.
METHODS: mtDNAcn was assessed with a TaqMan multiplex assay in granulocytes of 43 male combat veterans with (n=43) or without (n=44) PTSD. Twenty of the PTSD subjects had co-morbid major depressive disorder (MDD). The Clinician Administered PTSD Scale (CAPS), the Positive and Negative Affect Schedule (PANAS), the Early Trauma Inventory (ETI) and the Beck Depression Inventory II (BDI-II) were used for the clinical assessments. All analyses were corrected for age and BMI.
RESULTS: mtDNAcn was significantly lower in subjects with PTSD (p&amp;lt;0.05). Within the PTSD group, those with moderate PTSD...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1k0456d5</guid>
      <pubDate>Mon, 17 Sep 2018 00:00:00 +0000</pubDate>
      <author>
        <name>Bersani, Francesco Saverio</name>
      </author>
      <author>
        <name>Morley, Claire</name>
      </author>
      <author>
        <name>Lindqvist, Daniel</name>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
      <author>
        <name>Picard, Martin</name>
      </author>
      <author>
        <name>Yehuda, Rachel</name>
      </author>
      <author>
        <name>Flory, Janine</name>
      </author>
      <author>
        <name>Bierer, Linda M</name>
      </author>
      <author>
        <name>Makotkine, Iouri</name>
      </author>
      <author>
        <name>Abu-Amara, Duna</name>
      </author>
      <author>
        <name>Coy, Michelle</name>
      </author>
      <author>
        <name>Reus, Victor I</name>
        <uri>https://orcid.org/0000-0002-8193-5697</uri>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Marmar, Charles</name>
      </author>
      <author>
        <name>Wolkowitz, Owen M</name>
        <uri>https://orcid.org/0000-0003-0655-5042</uri>
      </author>
      <author>
        <name>Mellon, Synthia H</name>
      </author>
    </item>
    <item>
      <title>Longer leukocyte telomere length in Costa Rica's Nicoya Peninsula: A population-based study</title>
      <link>https://escholarship.org/uc/item/84j4j595</link>
      <description>Studies in humans suggest that leukocyte telomere length may act as a marker of biological aging. We investigated whether individuals in the Nicoya region of Costa Rica, known for exceptional longevity, had longer telomere length than those in other parts of the country. After controlling for age, age squared, rurality, rainy season and gender, the mean leukocyte telomere length in Nicoya was substantially longer (81 base pairs, p&amp;lt;0.05) than in other areas of Costa Rica, providing evidence of a biological pathway to which this notable longevity may be related. This relationship remains unchanged (79 base pairs, p&amp;lt;0.05) after statistically controlling for nineteen potential biological, dietary and social and demographic mediators. Thus the difference in the mean leukocyte telomere length that characterizes this unique region does not appear to be explainable by traditional behavioral and biological risk factors. More detailed examination of mean leukocyte telomere length...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/84j4j595</guid>
      <pubDate>Wed, 6 Apr 2016 00:00:00 +0000</pubDate>
      <author>
        <name>Rehkopf, David H</name>
      </author>
      <author>
        <name>Dow, William H</name>
        <uri>https://orcid.org/0000-0002-4080-1668</uri>
      </author>
      <author>
        <name>Rosero-Bixby, Luis</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
    </item>
    <item>
      <title>Seasonal variation of peripheral blood leukocyte telomere length in Costa Rica: A population‐based observational study</title>
      <link>https://escholarship.org/uc/item/0273p9q3</link>
      <description>&lt;h4&gt;Objectives&lt;/h4&gt;Peripheral blood leukocyte telomere length (LTL) is increasingly being used as a biomarker of aging, but its natural variation in human populations is not well understood. Several other biomarkers show seasonal variation, as do several determinants of LTL. We examined whether there was monthly variation in LTL in Costa Rica, a country with strong seasonal differences in precipitation and infection.&lt;h4&gt;Methods&lt;/h4&gt;We examined a longitudinal population-based cohort of 581 Costa Rican adults age 60 and above, from which blood samples were drawn between October 2006 and July 2008. LTL was assayed from these samples using the quantitative PCR method. Multivariate regression models were used to examine correlations between month of blood draw and LTL.&lt;h4&gt;Results&lt;/h4&gt;Telomere length from peripheral blood leukocytes varied by as much as 200 base pairs depending on month of blood draw, and this difference is not likely to be due to random variation. A moderate proportion...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0273p9q3</guid>
      <pubDate>Wed, 6 Apr 2016 00:00:00 +0000</pubDate>
      <author>
        <name>Rehkopf, David H</name>
      </author>
      <author>
        <name>Dow, William H</name>
        <uri>https://orcid.org/0000-0002-4080-1668</uri>
      </author>
      <author>
        <name>Rosero‐Bixby, Luis</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
    </item>
    <item>
      <title>Determinants of telomere attrition over 1 year in healthy older women: stress and health behaviors matter</title>
      <link>https://escholarship.org/uc/item/1912w1zd</link>
      <description>Telomere length, a reliable predictor of disease pathogenesis, can be affected by genetics, chronic stress and health behaviors. Cross-sectionally, highly stressed postmenopausal women have shorter telomeres, but only if they are inactive. However, no studies have prospectively examined telomere length change over a short period, and if rate of attrition is affected by naturalistic factors such as stress and engagement in healthy behaviors, including diet, exercise, and sleep. Here we followed healthy women over 1 year to test if major stressors that occurred over the year predicted telomere shortening, and whether engaging in healthy behaviors during this period mitigates this effect. In 239 postmenopausal, non-smoking, disease-free women, accumulation of major life stressors across a 1-year period predicted telomere attrition over the same period—for every major life stressor that occurred during the year, there was a significantly greater decline in telomere length over the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1912w1zd</guid>
      <pubDate>Thu, 7 May 2015 00:00:00 +0000</pubDate>
      <author>
        <name>Puterman, E</name>
      </author>
      <author>
        <name>Lin, J</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Krauss, J</name>
      </author>
      <author>
        <name>Blackburn, EH</name>
      </author>
      <author>
        <name>Epel, ES</name>
      </author>
    </item>
    <item>
      <title>Stress appraisals and cellular aging: A key role for anticipatory threat in the relationship between psychological stress and telomere length</title>
      <link>https://escholarship.org/uc/item/8px374kc</link>
      <description>Chronic psychological stress is a risk factor for multiple diseases of aging. Accelerated cellular aging as indexed by short telomere length has emerged as a potential common biological mechanism linking various forms of psychological stress and diseases of aging. Stress appraisals determine the degree and type of biological stress responses and altered stress appraisals may be a common psychological mechanism linking psychological stress and diseases of aging. However, no previous studies have examined the relationship between stress appraisals and telomere length. We exposed chronically stressed female caregivers and non-caregiving controls (N=50; M age=62.14±6.10) to a standardized acute laboratory stressor and measured their anticipatory and retrospective threat and challenge appraisals of the stressor. We hypothesized that threat and challenge appraisals would be associated with shorter and longer telomere length respectively, and that chronic caregiving stress would influence...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8px374kc</guid>
      <pubDate>Mon, 9 Feb 2015 00:00:00 +0000</pubDate>
      <author>
        <name>O’Donovan, Aoife</name>
      </author>
      <author>
        <name>Tomiyama, A Janet</name>
        <uri>https://orcid.org/0000-0002-2152-5813</uri>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Puterman, Eli</name>
      </author>
      <author>
        <name>Adler, Nancy E</name>
      </author>
      <author>
        <name>Kemeny, Margaret</name>
      </author>
      <author>
        <name>Wolkowitz, Owen M</name>
        <uri>https://orcid.org/0000-0003-0655-5042</uri>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
    </item>
    <item>
      <title>Does cellular aging relate to patterns of allostasis? An e`xamination of basal and stress reactive HPA axis activity and telomere length</title>
      <link>https://escholarship.org/uc/item/3g20d3sw</link>
      <description>Long-term exposure to stress and its physiological mediators, in particular cortisol, may lead to impaired telomere maintenance. In this study, we examine if greater cortisol responses to an acute stressor and/or dysregulated patterns of daily cortisol secretion are associated with shorter telomere length. Twenty-three postmenopausal women comprising caregivers for dementia partners (n=14) and age- and BMI-matched non-caregivers provided home sampling of cortisol-saliva samples at waking, 30 min after waking, and bedtime, and a 12-hour overnight urine collection. They were also exposed to an acute laboratory stressor throughout which they provided saliva samples. Peripheral blood mononuclear cells were isolated from a fasting blood sample and assayed for telomere length. As hypothesized, greater cortisol responses to the acute stressor were associated with shorter telomeres, as were higher overnight urinary free cortisol levels and flatter daytime cortisol slopes. While robust...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3g20d3sw</guid>
      <pubDate>Mon, 9 Feb 2015 00:00:00 +0000</pubDate>
      <author>
        <name>Tomiyama, A Janet</name>
        <uri>https://orcid.org/0000-0002-2152-5813</uri>
      </author>
      <author>
        <name>O'Donovan, Aoife</name>
        <uri>https://orcid.org/0000-0003-2353-7217</uri>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Puterman, Eli</name>
      </author>
      <author>
        <name>Lazaro, Alanie</name>
      </author>
      <author>
        <name>Chan, Jessica</name>
      </author>
      <author>
        <name>Dhabhar, Firdaus S</name>
      </author>
      <author>
        <name>Wolkowitz, Owen</name>
        <uri>https://orcid.org/0000-0003-0655-5042</uri>
      </author>
      <author>
        <name>Kirschbaum, Clemens</name>
      </author>
      <author>
        <name>Blackburn, Elizabeth</name>
      </author>
      <author>
        <name>Epel, Elissa</name>
      </author>
    </item>
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