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Association of mitochondrial DNA copy number with cardiometabolic diseases
- Liu, Xue;
- Longchamps, Ryan J;
- Wiggins, Kerri L;
- Raffield, Laura M;
- Bielak, Lawrence F;
- Zhao, Wei;
- Pitsillides, Achilleas;
- Blackwell, Thomas W;
- Yao, Jie;
- Guo, Xiuqing;
- Kurniansyah, Nuzulul;
- Thyagarajan, Bharat;
- Pankratz, Nathan;
- Rich, Stephen S;
- Taylor, Kent D;
- Peyser, Patricia A;
- Heckbert, Susan R;
- Seshadri, Sudha;
- Cupples, L Adrienne;
- Boerwinkle, Eric;
- Grove, Megan L;
- Larson, Nicholas B;
- Smith, Jennifer A;
- Vasan, Ramachandran S;
- Sofer, Tamar;
- Fitzpatrick, Annette L;
- Fornage, Myriam;
- Ding, Jun;
- Correa, Adolfo;
- Abecasis, Goncalo;
- Psaty, Bruce M;
- Wilson, James G;
- Levy, Daniel;
- Rotter, Jerome I;
- Bis, Joshua C;
- Consortium, TOPMed mtDNA Working Group in NHLBI Trans-Omics for Precision Medicine;
- Satizabal, Claudia L;
- Arking, Dan E;
- Liu, Chunyu
- et al.
Abstract
Mitochondrial DNA (mtDNA) is present in multiple copies in human cells. We evaluated cross-sectional associations of whole blood mtDNA copy number (CN) with several cardiometabolic disease traits in 408,361 participants of multiple ancestries in TOPMed and UK Biobank. Age showed a threshold association with mtDNA CN: among younger participants (<65 years of age), each additional 10 years of age was associated with 0.03 standard deviation (s.d.) higher level of mtDNA CN (P = 0.0014) versus a 0.14 s.d. lower level of mtDNA CN (P = 1.82 × 10-13) among older participants (≥65 years). At lower mtDNA CN levels, we found age-independent associations with increased odds of obesity (P = 5.6 × 10-238), hypertension (P = 2.8 × 10-50), diabetes (P = 3.6 × 10-7), and hyperlipidemia (P = 6.3 × 10-5). The observed decline in mtDNA CN after 65 years of age may be a key to understanding age-related diseases.
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