Abstract

IntroductionType 2 diabetes (T2D) is multifactorial involving lifestyle, environmental and genetic risk factors. This study aims to investigate the impact of genetic interactions with alcohol and diet quality on glycated haemoglobin A1c (HbA1c) independent of obesity, in a British population.MethodsCross‐sectional study of 14 089 white British participants from Airwave Health Monitoring Study and a subsample of 3733 participants with dietary data. A T2D genetic risk score (GRS) was constructed, and its interactions with diet on HbA1c were assessed.ResultsGRS was associated with a higher HbA1c% (β = 0.03, P < 0.0001) and a higher risk of prediabetes (OR = 1.09, P < 0.0001) and T2D (OR = 1.14, P = 0.006). The genetic effect on HbA1c% was significantly higher in obese participants (β = 1.88, P interaction = 0.03). A high intake of wholegrain attenuated the effect on HbA1c% in high‐risk individuals P interaction = 0.04.ConclusionThe genetic effect on HbA1c was almost doubled in obese individuals, compared with those with a healthy weight, and independent of weight, there was a modest offset on HbA1c in high‐genetic‐risk individuals consuming a diet high in wholegrain. This supports the importance of a healthy diet high in wholegrains and along with maintaining a healthy weight in controlling HbA1c among high‐genetic‐risk groups.

Highlights

  • We observed a greater effect of genetic risk score (GRS) on haemoglobin A1c (HbA1c) among obese participants (BMI

  • Well‐characterized occupational cohort, we found, among individuals of European ancestry at genetically high risk of diabetes, that consuming a high‐quality diet and high wholegrain intake was as‐ sociated with a beneficial modification of the genetic risk

  • The same study reported a reduced effect of Single nucleotide polymorphisms (SNP) rs10423928 (GIPR gene) on Type 2 diabetes (T2D) incidence in individuals who had the highest intake of carbohydrate (OR = 1.23, 95% confident inter‐ (CI): 5%‐39%) compared to those with the lowest carbohydrate intake (OR = 1.69, 95% CI: 29%‐86%)

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Summary

| METHODS

Worldwide over 382 million people are estimated to have type 2 di‐ abetes (T2D).[1]. People with T2D have a fivefold risk in developing cardiovascular disease (CVD) and are 1.6 times more likely to die prematurely, compared with those without T2D.2 Early intervention at the critical stage, prediabetes may halt the development of T2D and further reduce the risk of CVD and related premature mortality worldwide.[1]. SNPs are combined into genetic risk scores Lifestyle factors such as diet, alcohol and weight are modifiable key components in the development of T2D.2. Response to diet is variable, emerging evidence suggests that these lifestyle factors may modify the genetic effect on development of T2D.9-11. The aim of the study is to investigate associations between the combined effect of genetic variants and HbA1c among a white British population group, and if these associations are modified by interactions with lifestyle factors including diet quality (dietary pro‐ filing) and alcohol independent of obesity markers; body mass index (BMI) and waist circumference

| Study design and participants
| Ethics approval
| DISCUSSION
| Strengths and limitations of study
| Implications of findings and conclusion
Findings
International Diabetes Federation
Full Text
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