Gene-Based Elevated Triglycerides and Type 2 Diabetes Mellitus Risk in the Women's Genome Health Study.

Shafqat Ahmad, Samia Mora, Paul M Ridker, Frank B Hu, Daniel I Chasman
Author Information
  1. Shafqat Ahmad: From the Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, MA (S.A., F.B.H.).
  2. Samia Mora: Division of Preventive Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (S.A., S.M., P.M.R., D.I.C.).
  3. Paul M Ridker: Division of Preventive Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (S.A., S.M., P.M.R., D.I.C.).
  4. Frank B Hu: From the Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, MA (S.A., F.B.H.).
  5. Daniel I Chasman: Division of Preventive Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (S.A., S.M., P.M.R., D.I.C.).

Abstract

Objective- Higher triglyceride (TG) is a risk factor for incident type 2 diabetes mellitus (T2DM), but paradoxically, genetic susceptibility for higher TG has been associated with lower T2DM risk. There is also evidence that the genetic association may be modified by baseline TG. Whether such associations can be replicated and the interaction is selective for certain TG-rich lipoprotein particles remains to be explored. Approach and Results- Cox regression involving TG, TG-rich lipoprotein particles, and genetic determinants of TG was performed among 15 813 participants with baseline fasting status in the WGHS (Women's Genome Health Study), including 1453 T2DM incident cases during a mean 18.6 (SD=5.3) years of follow-up. A weighted, 40-single-nucleotide polymorphism TG genetic risk score was inversely associated with incident T2DM (hazard ratio [95% CI], 0.66 [0.58-0.75]/10-TG risk alleles; P<0.0001) with adjustment for baseline body mass index, HDL (high-density lipoprotein) cholesterol, and TG. TG-associated risk was higher among individuals in the low compared with the high 40-single-nucleotide polymorphism TG genetic risk score tertile (hazard ratio [95% CI], 1.98 [1.83-2.14] versus 1.68 [1.58-1.80] per mmol/L; P=0.0007). In TG-adjusted analysis, large and medium but not small TG-rich lipoprotein particles were associated with higher T2DM incidence for successively lower 40-single-nucleotide polymorphism TG genetic risk score tertiles, P=0.013, 0.012, and 0.620 across tertiles, respectively. Conclusions- Our results confirm the previous observations of the paradoxical associations of TG with T2DM while focusing attention on the larger TG-rich lipoprotein particle subfractions, suggesting their importance in clinical profiling of T2DM risk.

Keywords

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Grants

  1. R01 HL043851/NHLBI NIH HHS
  2. R21 NS104398/NINDS NIH HHS
  3. K08 HL094375/NHLBI NIH HHS
  4. UM1 CA182913/NCI NIH HHS
  5. R01 CA047988/NCI NIH HHS
  6. U01 CA182913/NCI NIH HHS
  7. R01 HL134811/NHLBI NIH HHS
  8. R01 EY021900/NEI NIH HHS
  9. R01 DK112940/NIDDK NIH HHS
  10. R01 HL080467/NHLBI NIH HHS
  11. K24 HL136852/NHLBI NIH HHS
  12. R21 NS092963/NINDS NIH HHS

MeSH Term

Aged
Diabetes Mellitus, Type 2
Female
Humans
Lipoproteins
Middle Aged
Polymorphism, Single Nucleotide
Proportional Hazards Models
Risk
Triglycerides
Women's Health

Chemicals

Lipoproteins
Triglycerides
lipoprotein triglyceride

Word Cloud

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