Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Randomized Controlled Trial
. 2024 Aug 1;73(8):1352-1360.
doi: 10.2337/db23-0761.

Increased Genetic Risk for β-Cell Failure Is Associated With β-Cell Function Decline in People With Prediabetes

Affiliations
Randomized Controlled Trial

Increased Genetic Risk for β-Cell Failure Is Associated With β-Cell Function Decline in People With Prediabetes

Liana K Billings et al. Diabetes. .

Abstract

Partitioned polygenic scores (pPS) have been developed to capture pathophysiologic processes underlying type 2 diabetes (T2D). We investigated the association of T2D pPS with diabetes-related traits and T2D incidence in the Diabetes Prevention Program. We generated five T2D pPS (β-cell, proinsulin, liver/lipid, obesity, lipodystrophy) in 2,647 participants randomized to intensive lifestyle, metformin, or placebo arms. Associations were tested with general linear models and Cox regression with adjustment for age, sex, and principal components. Sensitivity analyses included adjustment for BMI. Higher β-cell pPS was associated with lower insulinogenic index and corrected insulin response at 1-year follow-up with adjustment for baseline measures (effect per pPS SD -0.04, P = 9.6 × 10-7, and -8.45 μU/mg, P = 5.6 × 10-6, respectively) and with increased diabetes incidence with adjustment for BMI at nominal significance (hazard ratio 1.10 per SD, P = 0.035). The liver/lipid pPS was associated with reduced 1-year baseline-adjusted triglyceride levels (effect per SD -4.37, P = 0.001). There was no significant interaction between T2D pPS and randomized groups. The remaining pPS were associated with baseline measures only. We conclude that despite interventions for diabetes prevention, participants with a high genetic burden of the β-cell cluster pPS had worsening in measures of β-cell function.

PubMed Disclaimer

Conflict of interest statement

Duality of Interest. C.G.L. was an employee in the Division of Diabetes, Endocrinology, and Metabolic Diseases at the NIDDK, NIH, at the time this research was conducted and is currently an employee of Pfizer. McKesson BioServices and Matthews Media Group provided support services under subcontract with the Coordinating Center. No other potential conflicts of interest relevant to this article were reported.

Figures

Figure 1
Figure 1
Greater decline in insulin secretory response over 1 year in the highest quartile of β-cell cluster pPS. In participants in the highest quartile of β-cell cluster pPS compared with those in the lowest quartile, the adjusted means of measures of β-cell secretory response estimated with IGR (A) and CIR (B) both significantly decline from baseline to 1 year (P < 0.001). IGR (μU/mg) = (insulin30 min − insulin0 min) / (glucose30 min − glucose0 min). CIR = (100 × insulin30 min) / [glucose30-min × (glucose30-min − 70 mg/dL)].

References

    1. Menke A, Casagrande S, Geiss L, Cowie CC. Prevalence of and trends in diabetes among adults in the United States, 1988–2012. JAMA 2015;314:1021–1029 - PubMed
    1. Ligthart S, van Herpt TT, Leening MJ, et al. Lifetime risk of developing impaired glucose metabolism and eventual progression from prediabetes to type 2 diabetes: a prospective cohort study. Lancet Diabetes Endocrinol 2016;4:44–51 - PubMed
    1. Knowler WC, Barrett-Connor E, Fowler SE, et al.; Diabetes Prevention Program Research Group . Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin. N Engl J Med 2002;346:393–403 - PMC - PubMed
    1. Jablonski KA, McAteer JB, de Bakker PI, et al.; Diabetes Prevention Program Research Group . Common variants in 40 genes assessed for diabetes incidence and response to metformin and lifestyle intervention in the Diabetes Prevention Program. Diabetes 2010;59:2672–2681 - PMC - PubMed
    1. Billings LK, Jablonski KA, Ackerman RJ, et al.; Diabetes Prevention Program Research Group, Rockville . The influence of rare genetic variation in SLC30A8 on diabetes incidence and β-cell function. J Clin Endocrinol Metab 2014;99:E926–E930 - PMC - PubMed

Publication types

Grants and funding