1693-P: Association of Sleep and OSA Severity with Neurocognitive Function in the RISE Study

Diabetes(2023)

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摘要
Poor sleep and obstructive sleep apnea (OSA) have both been associated with worsening neurocognitive function. In the Restoring Insulin Secretion (RISE) Study, we assessed the relationship between presence and severity of OSA and cognition in treatment-naïve adults (n=179) with prediabetes or early T2D. A cognitive battery (CogState™ and story recall) assessed 1) psychomotor speed; 2) visual pattern separation; 3) visual attention and working memory; and 4) verbal learning and episodic memory. Wrist accelerometers worn for 7 days measured average sleep duration and efficiency. Other sleep outcomes were measured during one night of laboratory polysomnography. Linear regression models were fit to assess independent relationships between cognition and sleep measures. The cohort consisted of 44% females, 56% males; 53% white, 33% black, 6% Hispanic; age 54.7±8.9 years and BMI 34.7±5.4 kg/m2 (mean±SD). Based on ADA criteria, 73% had prediabetes and 27% had T2D. Sleep duration was 6.5±1.0 h; sleep efficiency was 85.9±7.5%; 26% had moderate OSA, 40% had severe OSA. After adjustment for age, sex, race/ethnicity, education, and BMI, higher sleep efficiency was associated with better visual pattern separation (as measured by the One Card Learning Test; p=0.039) but not with any other neurocognitive assessment. In the RISE cohort, measures of OSA severity (apnea-hypopnea index, oxygen desaturation index, sleep duration below 90% oxygen saturation, microarousal index) were not associated with baseline cognition. This cross-sectional analysis shows a high prevalence of moderate/severe OSA in treatment-naïve adults with prediabetes or early T2D. Although higher sleep efficiency was associated with better visual pattern separation, it was not associated with other measures of cognitive function. Further, OSA severity was not associated with measures of neurocognition. Disclosure K.A.Temple: None. A.H.Tjaden: None. D.Ehrmann: None. S.Manchanda: Advisory Panel; Inspire. S.Edelstein: None. T.S.Hannon: Advisory Panel; Eli Lilly and Company. S.Craft: None. B.Mokhlesi: None. Rise consortium: n/a. Funding American Diabetes Association (1-20-RISE-01 to S.E.); National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; U.S. Department of Veterans Affairs; Kaiser Permanente Southern California
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关键词
sleep,neurocognitive function,osa severity,rise
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