Genome-wide association study identifies common loci influencing circulating glycated hemoglobin (HbA1c) levels in non-diabetic subjects: the Long Life Family Study (LLFS)
- PMID: 24405752
- PMCID: PMC3965585
- DOI: 10.1016/j.metabol.2013.11.018
Genome-wide association study identifies common loci influencing circulating glycated hemoglobin (HbA1c) levels in non-diabetic subjects: the Long Life Family Study (LLFS)
Abstract
Objective: Glycated hemoglobin (HbA1c) is a stable index of chronic glycemic status and hyperglycemia associated with progressive development of insulin resistance and frank diabetes. It is also associated with premature aging and increased mortality. To uncover novel loci for HbA1c that are associated with healthy aging, we conducted a genome-wide association study (GWAS) using non-diabetic participants in the Long Life Family Study (LLFS), a study with familial clustering of exceptional longevity in the US and Denmark.
Methods: A total of 4088 non-diabetic subjects from the LLFS were used for GWAS discoveries, and a total of 8231 non-diabetic subjects from the Atherosclerosis Risk in Communities Study (ARIC, in the MAGIC Consortium) and the Health, Aging, and Body Composition Study (HABC) were used for GWAS replications. HbA1c was adjusted for age, sex, centers, 20 principal components, without and with BMI. A linear mixed effects model was used for association testing.
Results: Two known loci at GCK rs730497 (or rs2908282) and HK1 rs17476364 were confirmed (p<5e-8). Of 25 suggestive (5e-8<p<1e-5) loci, one known (G6PC2 rs560887, replication p=5e-5) and one novel (OR10R3P/SPTA1- rs12041363, replication p=1e-17) loci were replicated (p<0.0019). Similar findings resulted when HbA1c was further adjusted for BMI. Further validations are crucial for the remaining suggestive loci including the emerged variant near OR10R3P/SPTA1.
Conclusions: The analysis reconfirmed two known GWAS loci (GCK, HK1) and identified 25 suggestive loci including one reconfirmed variant in G6PC2 and one replicated variant near OR10R3P/SPTA1. Future focused survey of sequence elements containing mainly functional and regulatory variants may yield additional findings.
Keywords: Genome-wide association study; Glucose; Insulin resistance and diabetes; Non-enzymatic glycation; Premature aging processes.
Copyright © 2014 Elsevier Inc. All rights reserved.
Conflict of interest statement
The authors declare that there is no duality of interest associated with this manuscript.
Figures


Similar articles
-
Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study.PLoS Genet. 2008 Dec;4(12):e1000312. doi: 10.1371/journal.pgen.1000312. Epub 2008 Dec 19. PLoS Genet. 2008. PMID: 19096518 Free PMC article.
-
Novel Loci (EIF4A2, ADIPOQ, TPRG1) for Triglyceride / High-density Lipoprotein Cholesterol Ratio Longitudinal Change (ΔTHR) among Subjects without Type 2 Diabetes: Evidence from the Long Life Family Study (LLFS) and the Framingham Heart Study (FHS) Offspring Cohort (OS).medRxiv [Preprint]. 2024 Jun 19:2024.06.18.24309120. doi: 10.1101/2024.06.18.24309120. medRxiv. 2024. PMID: 38947029 Free PMC article. Preprint.
-
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.Diabetes. 2010 Dec;59(12):3229-39. doi: 10.2337/db10-0502. Epub 2010 Sep 21. Diabetes. 2010. PMID: 20858683 Free PMC article.
-
Impact of Genetic Determinants of HbA1c on Type 2 Diabetes Risk and Diagnosis.Curr Diab Rep. 2018 Jun 21;18(8):52. doi: 10.1007/s11892-018-1022-4. Curr Diab Rep. 2018. PMID: 29931457 Review.
-
[Indicators of glycemic control --hemoglobin A1c (HbA1c), glycated albumin (GA), and 1,5-anhydroglucitol (1,5-AG)].Rinsho Byori. 2014 Jan;62(1):45-52. Rinsho Byori. 2014. PMID: 24724426 Review. Japanese.
Cited by
-
Genome-wide meta-analysis in Japanese populations identifies novel variants at the TMC6-TMC8 and SIX3-SIX2 loci associated with HbA1c.Sci Rep. 2017 Nov 23;7(1):16147. doi: 10.1038/s41598-017-16493-0. Sci Rep. 2017. PMID: 29170429 Free PMC article.
-
Genetic associations for two biological age measures point to distinct aging phenotypes.Aging Cell. 2021 Jun;20(6):e13376. doi: 10.1111/acel.13376. Epub 2021 May 26. Aging Cell. 2021. PMID: 34038024 Free PMC article.
-
Determination of individual type 2 diabetes risk profile in the North East Indian population & its association with anthropometric parameters.Indian J Med Res. 2019 Oct;150(4):390-398. doi: 10.4103/ijmr.IJMR_888_17. Indian J Med Res. 2019. PMID: 31823921 Free PMC article.
-
Genetic Signatures of Glucose Homeostasis: Synergistic Interplay With Long-Term Exposure to Cigarette Smoking in Development of Primary Colorectal Cancer Among African American Women.Clin Transl Gastroenterol. 2021 Oct 5;12(10):e00412. doi: 10.14309/ctg.0000000000000412. Clin Transl Gastroenterol. 2021. PMID: 34608882 Free PMC article.
-
A genome-wide association study identifies genetic determinants of hemoglobin glycation index with implications across sex and ethnicity.Front Endocrinol (Lausanne). 2024 Oct 28;15:1473329. doi: 10.3389/fendo.2024.1473329. eCollection 2024. Front Endocrinol (Lausanne). 2024. PMID: 39530122 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
- R01 AG032319/AG/NIA NIH HHS/United States
- U01 AG023744/AG/NIA NIH HHS/United States
- R01 HL059367/HL/NHLBI NIH HHS/United States
- P30 AG034424/AG/NIA NIH HHS/United States
- U01AG023712/AG/NIA NIH HHS/United States
- K01DK076595/DK/NIDDK NIH HHS/United States
- R21 DK080294/DK/NIDDK NIH HHS/United States
- U19AG023122/AG/NIA NIH HHS/United States
- R01HL086694/HL/NHLBI NIH HHS/United States
- HHSN268201100012C/HL/NHLBI NIH HHS/United States
- UL1RR025005/RR/NCRR NIH HHS/United States
- U01 AG023712/AG/NIA NIH HHS/United States
- HHSN268201100009I/HL/NHLBI NIH HHS/United States
- P30 AG024827/AG/NIA NIH HHS/United States
- R01HL59367/HL/NHLBI NIH HHS/United States
- HHSN268201100010C/HL/NHLBI NIH HHS/United States
- UL1 RR025005/RR/NCRR NIH HHS/United States
- N01 AG062101/AG/NIA NIH HHS/United States
- HHSN268201100008C/HL/NHLBI NIH HHS/United States
- UL1 TR001079/TR/NCATS NIH HHS/United States
- HHSN268201100005G/HL/NHLBI NIH HHS/United States
- U19 AG023122/AG/NIA NIH HHS/United States
- HHSN268201100008I/HL/NHLBI NIH HHS/United States
- HHSN268201100007C/HL/NHLBI NIH HHS/United States
- P50 AG008702/AG/NIA NIH HHS/United States
- K01067207/PHS HHS/United States
- HHSN268201100011I/HL/NHLBI NIH HHS/United States
- P30 DK079637/DK/NIDDK NIH HHS/United States
- HHSN268201100011C/HL/NHLBI NIH HHS/United States
- R01 HL086694/HL/NHLBI NIH HHS/United States
- 1R01AG032098-01A1/AG/NIA NIH HHS/United States
- U01AG023746/AG/NIA NIH HHS/United States
- K24 AG025727/AG/NIA NIH HHS/United States
- N01 AG062106/AG/NIA NIH HHS/United States
- HHSN268200625226C/PHS HHS/United States
- U01 HG004402/HG/NHGRI NIH HHS/United States
- U01HG004402/HG/NHGRI NIH HHS/United States
- R01 AG032098/AG/NIA NIH HHS/United States
- U01AG023744/AG/NIA NIH HHS/United States
- K01 DK076595/DK/NIDDK NIH HHS/United States
- HHSN268200782096C/HG/NHGRI NIH HHS/United States
- HHSN268201100006C/HL/NHLBI NIH HHS/United States
- R01HL087641/HL/NHLBI NIH HHS/United States
- U01 AG023749/AG/NIA NIH HHS/United States
- R21 HL114237/HL/NHLBI NIH HHS/United States
- HHSN268201100005I/HL/NHLBI NIH HHS/United States
- N01 AG062103/AG/NIA NIH HHS/United States
- U01AG023755/AG/NIA NIH HHS/United States
- R21HL114237/HL/NHLBI NIH HHS/United States
- U01 AG023755/AG/NIA NIH HHS/United States
- U01AG023749/AG/NIA NIH HHS/United States
- K24AG025727/AG/NIA NIH HHS/United States
- ImNIH/Intramural NIH HHS/United States
- U01 AG023746/AG/NIA NIH HHS/United States
- HHSN268201100009C/HL/NHLBI NIH HHS/United States
- HHSN268201100005C/HL/NHLBI NIH HHS/United States
- HHSN268201100007I/HL/NHLBI NIH HHS/United States
- R21DK080294/DK/NIDDK NIH HHS/United States
- R01AG032319/AG/NIA NIH HHS/United States
- R01 HL087641/HL/NHLBI NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Miscellaneous