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Objective and Subjective Sleep Patterns in Adults With Maturity-Onset Diabetes of the Young (MODY).

AbstractOBJECTIVE:
To examine sleep patterns in adults with maturity-onset diabetes of the young (MODY).
RESEARCH DESIGN AND METHODS:
Adults with glucokinase (GCK)-MODY and transcription factor (TF)-related MODY (HNF1A, HNF1B, HNF4A) were recruited (n = 24; age 46.0 years, 79% women, BMI 24.7 kg/m2) from The University of Chicago's Monogenic Diabetes Registry. Sleep patterns were assessed by 2-week wrist actigraphy (total 315 nights), one night of a home sleep apnea test, and validated surveys.
RESULTS:
Overall, compared with established criteria, 29% of participants had sleep latency ≥15 min, 38% had sleep efficiency ≤85%, 46% had wake after sleep onset >40 min, all indicating poor objective sleep quality. Among all participants, 54% had a sleep duration below the recommended minimum of 7 h, 88% reported poor sleep quality, 58% had obstructive sleep apnea, and 71% reported insomnia. Compared with GCK-MODY, participants with TF-related MODY had poorer objective sleep quality and increased night-to-night variability in sleep patterns.
CONCLUSIONS:
Sleep disturbances appear to be common in adults with MODY despite absent traditional risk factors for sleep disorders. Future research investigating the sleep-diabetes relationship is warranted in this population.
AuthorsMarilyn Arosemena, Maria V Salguero, Rochelle N Naylor, Kristen Wroblewski, Esra Tasali, Louis H Philipson
JournalDiabetes care (Diabetes Care) Vol. 46 Issue 3 Pg. 608-612 (03 01 2023) ISSN: 1935-5548 [Electronic] United States
PMID36637968 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural)
Copyright© 2023 by the American Diabetes Association.
Chemical References
  • Glucokinase
  • Hepatocyte Nuclear Factor 1-alpha
Topics
  • Female
  • Humans
  • Male
  • Middle Aged
  • Diabetes Mellitus, Type 2 (complications, epidemiology)
  • Glucokinase (genetics)
  • Hepatocyte Nuclear Factor 1-alpha (genetics)
  • Mutation
  • Risk Factors
  • Sleep
  • Sleep Disorders, Intrinsic (etiology)

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