Obstructive Sleep Apnea, Glucose Tolerance, and beta-Cell Function in Adults With Prediabetes or Untreated Type 2 Diabetes in the Restoring Insulin Secretion (RISE) Study

Publication Description
OBJECTIVE: Obstructive sleep apnea (OSA) is associated with insulin resistance and has been described as a risk factor for type 2 diabetes. Whether OSA adversely impacts pancreatic islet beta-cell function remains unclear. We aimed to investigate the association of OSA and short sleep duration with beta-cell function in overweight/obese adults with prediabetes or recently diagnosed, treatment-naive type 2 diabetes. RESEARCH DESIGN AND METHODS: Two hundred twenty-one adults (57.5% men, age 54.5 +/- 8.7 years, BMI 35.1 +/- 5.5 kg/m(2)) completed 1 week of wrist actigraphy and 1 night of polysomnography before undergoing a 3-h oral glucose tolerance test (OGTT) and a two-step hyperglycemic clamp. Associations of measures of OSA and actigraphy-derived sleep duration with HbA1c, OGTT-derived outcomes, and clamp-derived outcomes were evaluated with adjusted regression models. RESULTS: Mean +/- SD objective sleep duration by actigraphy was 6.6 +/- 1.0 h/night. OSA, defined as an apnea-hypopnea index (AHI) of five or more events per hour, was present in 89% of the participants (20% mild, 28% moderate, 41% severe). Higher AHI was associated with higher HbA1c (P = 0.007). However, OSA severity, measured either by AHI as a continuous variable or by categories of OSA severity, and sleep duration (continuous or /=6 h) were not associated with fasting glucose, 2-h glucose, insulin sensitivity, or beta-cell responses. CONCLUSIONS: In this baseline cross-sectional analysis of the RISE clinical trial of adults with prediabetes or recently diagnosed, untreated type 2 diabetes, the prevalence of OSA was high. Although some measures of OSA severity were associated with HbA1c, OSA severity and sleep duration were not associated with measures of insulin sensitivity or beta-cell responses.

Primary Author
Mokhlesi,B.
Tjaden,A. H.
Temple,K. A.
Edelstein,S. L.
Sam,S.
Nadeau,K. J.
Hannon,T. S.
Manchanda,S.
Mather,K. J.
Kahn,S. E.
Ehrmann,D. A.
Van Cauter,E.
RISE Consortium

Author Address
University of Chicago, Chicago, IL [email protected].; George Washington University Biostatistics Center (RISE Coordinating Center), Rockville, MD.; University of Chicago, Chicago, IL.; George Washington University Biostatistics(TRUNCATED)

Volume
44

Issue
4

Start Page
993

Other Pages
1001

Publisher
by the American Diabetes Association

Author Address
University of Chicago, Chicago, IL [email protected].; George Washington University Biostatistics Center (RISE Coordinating Center), Rockville, MD.; University of Chicago, Chicago, IL.; George Washington University Biostatistics(TRUNCATED)

PMID
33547205

PMCID
PMC7985427



Reference Type
Journal Article

Periodical Full
Diabetes care

Publication Year
2021

Publication Date
1-Apr

Place of Publication
United States

ISSN/ISBN
1935-5548

Document Object Index
10.2337/dc20-2127 [doi]

Accession Number
PMID: 33547205