Chronic stress, inflammation, and glucose regulation in U.S. Hispanics from the HCHS/SOL Sociocultural Ancillary Study
Diabetes prevalence is rising rapidly, and diabetes disproportionately affects Hispanics and other underserved groups. Chronic stress may contribute to diabetes risk, but few studies have examined this relationship in U.S. Hispanics. We examined associations of chronic stress with fasting glucose, g...
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Published in | Psychophysiology Vol. 52; no. 8; pp. 1071 - 1079 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Blackwell Publishing Ltd
01.08.2015
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Abstract | Diabetes prevalence is rising rapidly, and diabetes disproportionately affects Hispanics and other underserved groups. Chronic stress may contribute to diabetes risk, but few studies have examined this relationship in U.S. Hispanics. We examined associations of chronic stress with fasting glucose, glucose tolerance, and glycosylated hemoglobin (HbA1c) in Hispanics without diabetes, and also assessed indirect effects of stress through inflammation (CRP). Participants were 3,923 men and women, aged 18–74, without diabetes, from the four U.S. field centers (Bronx, NY; Chicago, IL; Miami, FL; San Diego, CA) of the Hispanic Community Health Study/Study of Latinos (HCHS/SOL) Sociocultural Ancillary study. Participants completed a measure of chronic life stress and a physical exam with oral glucose tolerance test. In a multivariate regression analysis with adjustment for demographic and health covariates, higher chronic stress was related to higher fasting glucose (standardized regression coefficient: β = .09, p < .01), postload glucose (β = .07, p < .05), and HbA1c levels (β = .08, p < .01). However, there was no indirect effect of stress through inflammation. Findings suggest that higher chronic stress is associated with poorer glucose regulation in Hispanics, prior to the onset of a clinical diabetes diagnosis. |
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AbstractList | Diabetes prevalence is rising rapidly, and diabetes disproportionately affects Hispanics and other underserved groups. Chronic stress may contribute to diabetes risk, but few studies have examined this relationship in U.S. Hispanics. We examined associations of chronic stress with fasting glucose, glucose tolerance, and glycosylated hemoglobin (HbA1c) in Hispanics without diabetes, and also assessed indirect effects of stress through inflammation (CRP). Participants were 3,923 men and women, aged 18-74, without diabetes, from the four U.S. field centers (Bronx, NY; Chicago, IL; Miami, FL; San Diego, CA) of the Hispanic Community Health Study/Study of Latinos (HCHS/SOL) Sociocultural Ancillary study. Participants completed a measure of chronic life stress and a physical exam with oral glucose tolerance test. In a multivariate regression analysis with adjustment for demographic and health covariates, higher chronic stress was related to higher fasting glucose (standardized regression coefficient: β = .09, p < .01), postload glucose (β = .07, p < .05), and HbA1c levels (β = .08, p < .01). However, there was no indirect effect of stress through inflammation. Findings suggest that higher chronic stress is associated with poorer glucose regulation in Hispanics, prior to the onset of a clinical diabetes diagnosis. Diabetes prevalence is rising rapidly, and diabetes disproportionately affects Hispanics and other underserved groups. Chronic stress may contribute to diabetes risk, but few studies have examined this relationship in U.S. Hispanics. We examined associations of chronic stress with fasting glucose, glucose tolerance, and glycosylated hemoglobin (HbA1c) in Hispanics without diabetes, and also assessed indirect effects of stress through inflammation (CRP). Participants were 3,923 men and women, aged 18-74, without diabetes, from the four U.S. field centers (Bronx, NY; Chicago, IL; Miami, FL; San Diego, CA) of the Hispanic Community Health Study/Study of Latinos (HCHS/SOL) Sociocultural Ancillary study. Participants completed a measure of chronic life stress and a physical exam with oral glucose tolerance test. In a multivariate regression analysis with adjustment for demographic and health covariates, higher chronic stress was related to higher fasting glucose (standardized regression coefficient: [beta]=.09, p<.01), postload glucose ([beta]=.07, p<.05), and HbA1c levels ([beta]=.08, p<.01). However, there was no indirect effect of stress through inflammation. Findings suggest that higher chronic stress is associated with poorer glucose regulation in Hispanics, prior to the onset of a clinical diabetes diagnosis. Diabetes prevalence is rising rapidly, and diabetes disproportionately affects Hispanics and other underserved groups. Chronic stress may contribute to diabetes risk, but few studies have examined this relationship in U.S. Hispanics. We examined associations of chronic stress with fasting glucose, glucose tolerance, and glycosylated hemoglobin (HbA1c) in Hispanics without diabetes, and also assessed indirect effects of stress through inflammation (CRP). Participants were 3,923 men and women, aged 18–74, without diabetes, from the four U.S. field centers (Bronx, NY; Chicago, IL; Miami, FL; San Diego, CA) of the Hispanic Community Health Study/Study of Latinos (HCHS/SOL) Sociocultural Ancillary study. Participants completed a measure of chronic life stress and a physical exam with oral glucose tolerance test. In a multivariate regression analysis with adjustment for demographic and health covariates, higher chronic stress was related to higher fasting glucose (standardized regression coefficient: β = .09, p < .01), postload glucose (β = .07, p < .05), and HbA1c levels (β = .08, p < .01). However, there was no indirect effect of stress through inflammation. Findings suggest that higher chronic stress is associated with poorer glucose regulation in Hispanics, prior to the onset of a clinical diabetes diagnosis. Diabetes prevalence is rising rapidly, and diabetes disproportionately affects Hispanics and other underserved groups. Chronic stress may contribute to diabetes risk, but few studies have examined this relationship in U.S. Hispanics. We examined associations of chronic stress with fasting glucose, glucose tolerance, and glycosylated hemoglobin (HbA1c) in Hispanics without diabetes, and also assessed indirect effects of stress through inflammation (CRP). Participants were 3923 men and women, aged 18-74, without diabetes, from the four U.S. field centers (Bronx, NY; Chicago, IL; Miami, FL; San Diego, CA) of the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)-Sociocultural Ancillary study. Participants completed a measure of chronic life stress and a physical exam with oral glucose tolerance test. In a multivariate regression analysis with adjustment for demographic and health covariates, higher chronic stress was related to higher fasting glucose (standardized regression coefficient: β=.09, p<0.01), post load glucose (β=.07, p<0.05), and HbA1c levels (β=.08, p<0.01). However, there was no indirect effect of stress through inflammation. Findings suggest that higher chronic stress is associated with poorer glucose regulation in Hispanics, prior to the onset of a clinical diabetes diagnosis. |
Author | Mills, Paul J. Penedo, Frank J. Isasi, Carmen R. Llabre, Maria M. Giacinto, Rebeca E. Sotres-Alvarez, Daniela Carnethon, Mercedes Schneiderman, Neil Teng, Yanping Gallo, Linda C. Roesch, Scott C. McCurley, Jessica L. |
AuthorAffiliation | 4 Department of Preventive Medicine, Feinberg School of Medicine, Northwestern University 1 SDSU/UCSD Joint Doctoral Program in Clinical Psychology, University of California, San Diego 6 Department of Epidemiology and Population Health, Albert Einstein College of Medicine 7 Collaborative Studies Coordinating Center, Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina at Chapel Hill 5 SDSU/UCSD Joint Doctoral Program in Global Health 9 Department of Medical Social Sciences, Feinberg School of Medicine, Northwestern University 8 Department of Psychology, University of Miami 3 Department of Psychology, San Diego State University 2 Department of Psychiatry, University of California, San Diego |
AuthorAffiliation_xml | – name: 4 Department of Preventive Medicine, Feinberg School of Medicine, Northwestern University – name: 3 Department of Psychology, San Diego State University – name: 8 Department of Psychology, University of Miami – name: 7 Collaborative Studies Coordinating Center, Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina at Chapel Hill – name: 1 SDSU/UCSD Joint Doctoral Program in Clinical Psychology, University of California, San Diego – name: 2 Department of Psychiatry, University of California, San Diego – name: 5 SDSU/UCSD Joint Doctoral Program in Global Health – name: 6 Department of Epidemiology and Population Health, Albert Einstein College of Medicine – name: 9 Department of Medical Social Sciences, Feinberg School of Medicine, Northwestern University |
Author_xml | – sequence: 1 givenname: Jessica L. surname: McCurley fullname: McCurley, Jessica L. email: jlmccurl@ucsd.edu organization: SDSU/UCSD Joint Doctoral Program in Clinical Psychology, California, San Diego, USA – sequence: 2 givenname: Paul J. surname: Mills fullname: Mills, Paul J. organization: Department of Psychiatry, University of California, California, San DiegoSan Diego, USA – sequence: 3 givenname: Scott C. surname: Roesch fullname: Roesch, Scott C. organization: Department of Psychology, San Diego State University, California, San Diego, USA – sequence: 4 givenname: Mercedes surname: Carnethon fullname: Carnethon, Mercedes organization: Department of Preventive Medicine, Feinberg School of Medicine, Northwestern University, Illinois, Chicago, USA – sequence: 5 givenname: Rebeca E. surname: Giacinto fullname: Giacinto, Rebeca E. organization: SDSU/UCSD Joint Doctoral Program in Global Health, California, San Diego, USA – sequence: 6 givenname: Carmen R. surname: Isasi fullname: Isasi, Carmen R. organization: Department of Epidemiology and Population Health, Albert Einstein College of Medicine, New York, New York, USA – sequence: 7 givenname: Yanping surname: Teng fullname: Teng, Yanping organization: Collaborative Studies Coordinating Center, Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, North Carolina, Chapel Hill, USA – sequence: 8 givenname: Daniela surname: Sotres-Alvarez fullname: Sotres-Alvarez, Daniela organization: Collaborative Studies Coordinating Center, Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, North Carolina, Chapel Hill, USA – sequence: 9 givenname: Maria M. surname: Llabre fullname: Llabre, Maria M. organization: Department of Psychology, University of Miami, Florida, Coral Gables, USA – sequence: 10 givenname: Frank J. surname: Penedo fullname: Penedo, Frank J. organization: Department of Medical Social Sciences, Feinberg School of Medicine, Northwestern University, Illinois, Chicago, USA – sequence: 11 givenname: Neil surname: Schneiderman fullname: Schneiderman, Neil organization: Department of Psychology, University of Miami, Florida, Coral Gables, USA – sequence: 12 givenname: Linda C. surname: Gallo fullname: Gallo, Linda C. organization: Department of Psychology, San Diego State University, California, San Diego, USA |
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Notes | University of Miami - No. N01-HC65234 National Institute of Neurological Disorders and Stroke National Heart, Lung, and Blood Institute (NHLBI) istex:9AB285AA8B3D1A46A5F71D77FDEF80ABAB7FE5A7 National Institute of Diabetes and Digestive and Kidney Diseases National Center on Minority Health and Health Disparities ArticleID:PSYP12430 Albert Einstein College of Medicine - No. N01-HC65235 San Diego State University - No. N01-HC65237 National Institute of Deafness and Other Communications Disorders Office of Dietary Supplements ark:/67375/WNG-628DQ4GC-0 National Institute of Dental and Craniofacial Research University of North Carolina - No. N01-HC65233 MIH/NHLBI - No. RC2HL101649 Northwestern University - No. N01-HC65236 http://www.cscc.unc.edu/hchs The Hispanic Community Health Study/Study of Latinos is a collaborative investigation supported by contracts from the National Heart, Lung, and Blood Institute (NHLBI) to the University of North Carolina (N01‐HC65233), University of Miami (N01‐HC65234), Albert Einstein College of Medicine (N01‐HC65235), Northwestern University (N01‐HC65236), and San Diego State University (N01‐HC65237). The following institutes/centers/offices also contributed to funding the HCHS/SOL through the NHLBI: National Center on Minority Health and Health Disparities, the National Institute of Deafness and Other Communications Disorders, the National Institute of Dental and Craniofacial Research, the National Institute of Diabetes and Digestive and Kidney Diseases, the National Institute of Neurological Disorders and Stroke, and the Office of Dietary Supplements. The HCHS/SOL Sociocultural Ancillary Study was supported by MIH/NHLBI grant number RC2HL101649 (PIs LCG and FJP). The authors thank the staff and participants of HCHS/SOL and the HCHS/SOL Sociocultural Ancillary Study for their important contributions. A complete list of staff and investigators is available on the study website at ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
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Snippet | Diabetes prevalence is rising rapidly, and diabetes disproportionately affects Hispanics and other underserved groups. Chronic stress may contribute to... |
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SubjectTerms | Adolescent Adult Aged Blood Glucose - metabolism Diabetes Female Glucose Glucose Intolerance - metabolism Glucose Tolerance Test Glycated Hemoglobin - metabolism Health Surveys Hispanic Hispanic Americans Hispanic or Latino Humans Inflammation Inflammation - metabolism Insulin Male Middle Aged Risk Factors Stress Stress, Psychological - metabolism United States Young Adult |
Title | Chronic stress, inflammation, and glucose regulation in U.S. Hispanics from the HCHS/SOL Sociocultural Ancillary Study |
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