Diet and exercise interventions have made great strides in preventing and delaying T2D onset: benefits that surpass pharmacological interventions in some persons. Yet, variable responses from less intense, more affordable interventions and waning benefits over time are significant limitations. Identifying additional modifiable factors that can expand intervention options, beyond diet and exercise, are needed to reach heretofore resistant groups and to sustain metabolic benefits. One viable option is improving sleep. Multiple dimensions of sleep have been independently associated with T2D risk and poor glucose control in persons with T2D. Improved insulin sensitivity has been reported in a small community based daily sleep extension study (N= 16), as well as in a 2-day lab based sleep extension study using a personalized ?catch up? sleep intervention in healthy adults (N = 19,). Limited by small sample sizes, controlled lab conditions, and the exclusion of persons at greatest risk for T2D, the role of sleep in mitigating T2D risk remains uncertain. An important but unanswered question for tailoring sleep interventions is whether regular sleep timing should be prioritized. Given that irregular sleep-wake timing is widely prevalent, identifying the metabolic benefits or burdens of this sleep habit is critical. The proposed project in this K99/R00 award is a step toward independence in a program of research bridging circadian rhythms and metabolism to chrono-therapeutic interventions that mitigate type 2 diabetes (T2D) risk. Research: The study proposed in the K99 phase will leverage an existing data set to quantify the effects of irregular sleep timing on glucose regulation in persons with diabetes, prediabetes, and normoglycemia. This will elucidate individual differences in resiliency against or vulnerability to irregular sleep timing. Primary outcome measures will be hemoglobin A1c (for persons with diabetes and prediabetes) or insulin resistance (for persons with normoglycemia). The study proposed during the R00 phase will test the effects of a daily sleep extension intervention versus habitual sleep patterns on the percentage of time glucose is ? 140 mg/dL (n = 75 per group) in sleep restricted community-dwelling adults with pre-diabetes. Wearable sensor technologies (continuous glucose monitoring and accelerometry) will be used. This study will inform person- specific sleep interventions that improve glycemic responses, thus providing treatment for the prediabetic state. Training: To achieve overall career goals, the training plan will build upon the candidate's background in diabetes by affording her in-depth training in designing sleep interventions, wearable sensor technologies (specifically continuous glucose monitoring), and the analysis of large amounts of real time data. This training will also incorporate advancing her skills in writing and presenting scientific findings, as well as the skills to become a leader in the scientific community. A variety of approaches will be used to achieve these goals including formal coursework and structured one-on-one mentorship.

Public Health Relevance

Findings from this project will determine the viability of sleep as a treatment intervention for persons with prediabetes, thereby; expanding intervention options beyond calorie restricted diets and increased physical activity. The effects of widely prevalent sleep habits, such as restricted work day sleep and irregular sleep timing, on glucose regulation in community dwelling adults will be quantified. Raising opportunities for mitigating T2D risk based on individual sleep profiles may particularly benefit persons resistant to diet and exercise interventions, sustain the metabolic benefits reached by traditional lifestyle modification interventions, and open the door for a wide range of behavioral and environmental rhythm interventions to reduce T2D risk (e.g., light-dark exposure, timed restricted eating schedules).

Agency
National Institute of Health (NIH)
Institute
National Institute of Nursing Research (NINR)
Type
Career Transition Award (K99)
Project #
1K99NR017416-01
Application #
9431978
Study Section
National Institute of Nursing Research Initial Review Group (NRRC)
Program Officer
Diana, Augusto
Project Start
2018-01-04
Project End
2019-12-31
Budget Start
2018-01-04
Budget End
2018-12-31
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
New York University
Department
Type
Schools of Nursing
DUNS #
041968306
City
New York
State
NY
Country
United States
Zip Code
10012
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Matura, Lea Ann; Malone, Susan; Jaime-Lara, Rosario et al. (2018) A Systematic Review of Biological Mechanisms of Fatigue in Chronic Illness. Biol Res Nurs 20:410-421
Patterson, Freda; Malone, Susan Kohl; Grandner, Michael A et al. (2018) Interactive effects of sleep duration and morning/evening preference on cardiovascular risk factors. Eur J Public Health 28:155-161
Schroeder, Krista; Malone, Susan Kohl; McCabe, Ellen et al. (2018) Addressing the Social Determinants of Health: A Call to Action for School Nurses. J Sch Nurs 34:182-191