Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease
Background Recent studies have revealed sexually dimorphic associations between the carbamoyl-phosphate synthase 1 locus, intermediates of the metabolic pathway leading from choline to urea, and risk of coronary artery disease ( CAD ) in women. Based on evidence from the literature, the atheroprotective association with carbamoyl-phosphate synthase 1 could be mediated by the strong genetic effect of this locus on increased circulating glycine levels. Methods and Results We sought to identify additional genetic determinants of circulating glycine levels by carrying out a meta-analysis of genome-wide association study data in up to 30 118 subjects of European ancestry. Mendelian randomization and other analytical approaches were used to determine whether glycine-associated variants were associated with CAD and traditional risk factors. Twelve loci were significantly associated with circulating glycine levels, 7 of which were not previously known to be involved in glycine metabolism ( ACADM , PHGDH , COX 18- ADAMTS 3, PSPH , TRIB 1, PTPRD , and ABO ). Glycine-raising alleles at several loci individually exhibited directionally consistent associations with decreased risk of CAD . However, these effects could not be attributed directly to glycine because of associations with other CAD -related traits. By comparison, genetic models that only included the 2 variants directly involved in glycine degradation and for which there were no other pleiotropic associations were not associated with risk of CAD or blood pressure, lipid levels, and obesity-related traits. Conclusions These results provide additional insight into the genetic architecture of glycine metabolism, but do not yield conclusive evidence for a causal relationship between circulating levels of this amino acid and risk of CAD in humans.
Authors
- Michael Boehnke (ORCID: https://orcid.org/0000-0002-6442-7754)
- Janet Gukasyan
- Qiong Jia (ORCID: https://orcid.org/0000-0002-3063-2346)
- Johannes Kettunen (ORCID: https://orcid.org/0000-0002-3345-491X)
- Zeneng Wang (ORCID: https://orcid.org/0000-0002-6455-8228)
- Stanley L. Hazen (ORCID: https://orcid.org/0000-0001-7124-6639)
- Jaana Hartiala (ORCID: https://orcid.org/0000-0003-4883-9318)
- Karen L. Mohlke (ORCID: https://orcid.org/0000-0001-6721-153X)
- Markus Perola (ORCID: https://orcid.org/0000-0003-4842-1667)
- Olli Tuomas Raitakari (ORCID: https://orcid.org/0000-0001-9365-3702)
- Jorma S.A. Viikari (ORCID: https://orcid.org/0000-0001-6452-010X)
- Olga Anufrieva
- Hooman Allayee (ORCID: https://orcid.org/0000-0002-2384-5239)
- Terho J. Lehtimäki (ORCID: https://orcid.org/0000-0002-2555-4427)
- Oliver Fiehn (ORCID: https://orcid.org/0000-0002-6261-8928)
- Qin Wang (ORCID: https://orcid.org/0000-0001-8100-4852)
- Yi Han (ORCID: https://orcid.org/0000-0001-9673-441X)
- Markku Laakso (ORCID: https://orcid.org/0000-0002-3394-7749)
- Pin Huang
- Nicholas C. Woodward
Institutions
- University of North Carolina at Chapel Hill (US)
- University of Southern California (US)
- Cleveland Clinic (US)
- University of Helsinki (FI)
- Central South University (CN)
- Baker Heart and Diabetes Institute (AU)
- Tampere University of Applied Sciences (FI)
- University of Turku (FI)
- University of Eastern Finland (FI)
- Oulu University Hospital (FI)
- California Southern University (US)
- Turku University Hospital (FI)
- University of California System (US)
- Finnish Institute for Health and Welfare (FI)
- Helsinki Art Museum (FI)
- Tampere University (FI)
- Statistical Service (CY)
- Xiangya Hospital Central South University (CN)
- Imperial College London (GB)
- University of Tartu (EE)
- University of Oulu (FI)
Publication Details
- Published
- 2025-11-07
- DOI
- https://doi.org/10.17615/j2v7-dz26
- Primary Topic
- Metabolism and Genetic Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00