R01HL160619
Project Grant
Overview
Grant Description
Disrupted Sleep in Somali Americans: Implications for Hypertension Risk
Disrupted sleep is a major public health issue that independently increases the risk for cardiovascular disease (CVD). Blacks have higher rates of sleep deficiency, which are likely under-reported. However, the existing data primarily relate to individuals of West African ancestry, and our current knowledge of sleep disruption in Blacks cannot be readily applied to Somali Americans.
The majority of Somali immigrants have settled in Minnesota, which places our Minnesota-based research team in a unique position to comprehensively study the mechanisms and consequences of disrupted sleep as a mediator of cardiovascular health disparities in this population. Our preliminary data suggest that Somali Americans have a high likelihood of disrupted sleep, which may put them at increased risk for hypertension and other CVD.
Underlying sociocultural, behavioral, environmental, and biological factors likely contribute to an increased risk for sleep deficiencies. Therefore, we propose an interdisciplinary approach using a socioecological model informed by the National Institute on Minority Health and Health Disparities (NIMHD) research framework. This approach aims to determine the types and severity of undiagnosed sleep deficiencies in otherwise healthy Somali Americans, identify mechanisms contributing to their disrupted sleep, and examine the role of sleep deficiencies in raising blood pressure (BP).
Our central hypothesis is that Somali Americans will have a high likelihood of sleep deficiencies attributable in part to unique multilevel individual, psychosocial, contextual, and behavioral factors, which exert deleterious biological effects. To test this hypothesis, we propose the following aims:
Aim 1: Determine the types and severity of previously undiagnosed sleep deficiencies in otherwise healthy Somali Americans.
Hypothesis 1: Somali Americans have a high (>50%) likelihood of previously undiagnosed sleep deficiencies, including short sleep (<6 hours), insomnia, and obstructive sleep apnea.
Aim 2: Apply the NIMHD research framework to define psychosocial, behavioral, environmental, and biological mechanisms mediating sleep deficiencies in Somali Americans.
Hypothesis 2: Unique multilevel individual, cultural, and environmental risk and protective factors play a mechanistic role in mediating an increased likelihood of disrupted sleep in Somali Americans.
Aim 3: Examine the relationship between sleep deficiencies and increased BP in Somali Americans.
Hypothesis 3: BP during wakefulness and/or sleep will be increased in those subjects with disrupted sleep, commensurate with the type and severity of sleep deficiency, and moderated by factors such as sex and age.
The expected outcome of this proposal will be a mechanistic pathway incorporating the NIMHD research framework to identify psychosocial, behavioral, contextual, and biological factors mediating sleep deficiencies and related increases in BP, and consequently hypertension risk. This research will address important knowledge gaps in understanding sleep-related health disparities and their consequences in Somali Americans.
Disrupted sleep is a major public health issue that independently increases the risk for cardiovascular disease (CVD). Blacks have higher rates of sleep deficiency, which are likely under-reported. However, the existing data primarily relate to individuals of West African ancestry, and our current knowledge of sleep disruption in Blacks cannot be readily applied to Somali Americans.
The majority of Somali immigrants have settled in Minnesota, which places our Minnesota-based research team in a unique position to comprehensively study the mechanisms and consequences of disrupted sleep as a mediator of cardiovascular health disparities in this population. Our preliminary data suggest that Somali Americans have a high likelihood of disrupted sleep, which may put them at increased risk for hypertension and other CVD.
Underlying sociocultural, behavioral, environmental, and biological factors likely contribute to an increased risk for sleep deficiencies. Therefore, we propose an interdisciplinary approach using a socioecological model informed by the National Institute on Minority Health and Health Disparities (NIMHD) research framework. This approach aims to determine the types and severity of undiagnosed sleep deficiencies in otherwise healthy Somali Americans, identify mechanisms contributing to their disrupted sleep, and examine the role of sleep deficiencies in raising blood pressure (BP).
Our central hypothesis is that Somali Americans will have a high likelihood of sleep deficiencies attributable in part to unique multilevel individual, psychosocial, contextual, and behavioral factors, which exert deleterious biological effects. To test this hypothesis, we propose the following aims:
Aim 1: Determine the types and severity of previously undiagnosed sleep deficiencies in otherwise healthy Somali Americans.
Hypothesis 1: Somali Americans have a high (>50%) likelihood of previously undiagnosed sleep deficiencies, including short sleep (<6 hours), insomnia, and obstructive sleep apnea.
Aim 2: Apply the NIMHD research framework to define psychosocial, behavioral, environmental, and biological mechanisms mediating sleep deficiencies in Somali Americans.
Hypothesis 2: Unique multilevel individual, cultural, and environmental risk and protective factors play a mechanistic role in mediating an increased likelihood of disrupted sleep in Somali Americans.
Aim 3: Examine the relationship between sleep deficiencies and increased BP in Somali Americans.
Hypothesis 3: BP during wakefulness and/or sleep will be increased in those subjects with disrupted sleep, commensurate with the type and severity of sleep deficiency, and moderated by factors such as sex and age.
The expected outcome of this proposal will be a mechanistic pathway incorporating the NIMHD research framework to identify psychosocial, behavioral, contextual, and biological factors mediating sleep deficiencies and related increases in BP, and consequently hypertension risk. This research will address important knowledge gaps in understanding sleep-related health disparities and their consequences in Somali Americans.
Awardee
Funding Goals
THE NATIONAL CENTER ON SLEEP DISORDERS RESEARCH (NCSDR) SUPPORTS RESEARCH AND RESEARCH TRAINING RELATED TO SLEEP DISORDERED BREATHING, AND THE FUNDAMENTAL FUNCTIONS OF SLEEP AND CIRCADIAN RHYTHMS. THE CENTER ALSO STEWARDS SEVERAL FORUMS THAT FACILITATE THE COORDINATION OF SLEEP RESEARCH ACROSS NIH, OTHER FEDERAL AGENCIES AND OUTSIDE ORGANIZATIONS, INCLUDING THE SLEEP DISORDERS RESEARCH ADVISORY BOARD AND AN NIH-WIDE SLEEP RESEARCH COORDINATING COMMITTEE. THE CENTER ALSO PARTICIPATES IN THE TRANSLATION OF NEW SLEEP RESEARCH FINDINGS FOR DISSEMINATION TO HEALTH CARE PROFESSIONALS AND THE PUBLIC. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, USE SMALL BUSINESS TO MEET FEDERAL RESEARCH AND DEVELOPMENT NEEDS, FOSTER AND ENCOURAGE PARTICIPATION IN INNOVATION AND ENTREPRENEURSHIP BY SOCIALLY AND ECONOMICALLY DISADVANTAGED PERSONS, AND INCREASE PRIVATE-SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT FUNDING. SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, FOSTER TECHNOLOGY TRANSFER THROUGH COOPERATIVE R&D BETWEEN SMALL BUSINESSES AND RESEARCH INSTITUTIONS, AND INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL R&D.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Rochester,
Minnesota
559050001
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 294% from $787,153 to $3,097,975.
Mayo Clinic was awarded
Somali Americans' Sleep Disruption and Hypertension Risk Study
Project Grant R01HL160619
worth $3,097,975
from National Heart Lung and Blood Institute in June 2022 with work to be completed primarily in Rochester Minnesota United States.
The grant
has a duration of 4 years and
was awarded through assistance program 93.837 Cardiovascular Diseases Research.
The Project Grant was awarded through grant opportunity NIH Research Project Grant (Parent R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 7/3/25
Period of Performance
6/10/22
Start Date
5/31/26
End Date
Funding Split
$3.1M
Federal Obligation
$0.0
Non-Federal Obligation
$3.1M
Total Obligated
Activity Timeline
Transaction History
Modifications to R01HL160619
Additional Detail
Award ID FAIN
R01HL160619
SAI Number
R01HL160619-763189215
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Nonprofit With 501(c)(3) IRS Status (Other Than An Institution Of Higher Education)
Awarding Office
75NH00 NIH National Heart, Lung, and Blood Institute
Funding Office
75NH00 NIH National Heart, Lung, and Blood Institute
Awardee UEI
Y2K4F9RPRRG7
Awardee CAGE
5A021
Performance District
MN-01
Senators
Amy Klobuchar
Tina Smith
Tina Smith
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Heart, Lung, and Blood Institute, National Institutes of Health, Health and Human Services (075-0872) | Health research and training | Grants, subsidies, and contributions (41.0) | $1,568,590 | 100% |
Modified: 7/3/25