Metabolic factors and genetic risk mediate familial type 2 diabetes risk in the Framingham Heart Study

Diabetologia. 2015 May;58(5):988-96. doi: 10.1007/s00125-015-3498-7. Epub 2015 Jan 27.

Abstract

Aims/hypothesis: Type 2 diabetes mellitus in parents is a strong determinant of diabetes risk in their offspring. We hypothesise that offspring diabetes risk associated with parental diabetes is mediated by metabolic risk factors.

Methods: We studied initially non-diabetic participants of the Framingham Offspring Study. Metabolic risk was estimated using beta cell corrected insulin response (CIR), HOMA-IR or a count of metabolic syndrome components (metabolic syndrome score [MSS]). Dietary risk and physical activity were estimated using questionnaire responses. Genetic risk score (GRS) was estimated as the count of 62 type 2 diabetes risk alleles. The outcome of incident diabetes in offspring was examined across levels of parental diabetes exposure, accounting for sibling correlation and adjusting for age, sex and putative mediators. The proportion mediated was estimated by comparing regression coefficients for parental diabetes with (β adj) and without (β unadj) adjustments for CIR, HOMA-IR, MSS and GRS (percentage mediated = 1 - β adj / β unadj).

Results: Metabolic factors mediated 11% of offspring diabetes risk associated with parental diabetes, corresponding to a reduction in OR per diabetic parent from 2.13 to 1.96. GRS mediated 9% of risk, corresponding to a reduction in OR per diabetic parent from 2.13 to 1.99.

Conclusions/interpretation: Metabolic risk factors partially mediated offspring type 2 diabetes risk conferred by parental diabetes to a similar magnitude as genetic risk. However, a substantial proportion of offspring diabetes risk associated with parental diabetes remains unexplained by metabolic factors, genetic risk, diet and physical activity, suggesting that important familial influences on diabetes risk remain undiscovered.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adult
  • Aged
  • Diabetes Mellitus, Type 2 / epidemiology
  • Diabetes Mellitus, Type 2 / genetics
  • Diabetes Mellitus, Type 2 / metabolism*
  • Female
  • Genetic Predisposition to Disease*
  • Humans
  • Incidence
  • Insulin Resistance / physiology*
  • Life Style
  • Male
  • Metabolic Syndrome / epidemiology
  • Metabolic Syndrome / genetics
  • Metabolic Syndrome / metabolism*
  • Middle Aged
  • Risk