Diabetes distress mediates the relationship between depressive symptoms and glycaemic control among adults with type 2 diabetes: Findings from a multi‐site diabetes peer support intervention

Author:

Qian Yiqing12,Emmerling Dane A.1,Kowitt Sarah D.3,Ayala Guadalupe X.4,Cherrington Andrea L.5,Heisler Michele6,Safford Monika M.7,Tang Tricia S.8ORCID,Thom David H.9,Fisher Edwin B.12

Affiliation:

1. Department of Health Behavior, Gillings School of Global Public Health University of North Carolina at Chapel Hill Chapel Hill North Carolina USA

2. Peers for Progress, Gillings School of Global Public Health University of North Carolina at Chapel Hill North Carolina Chapel Hill USA

3. Department of Family Medicine, School of Medicine University of North Carolina at Chapel Hill Chapel Hill North Carolina USA

4. School of Public Health San Diego State University San Diego California USA

5. Division of Preventive Medicine, Department of Medicine University of Alabama at Birmingham Birmingham Alabama USA

6. VA Center for Clinical Management Research, Department of Health Behavior and Health Education, University of Michigan School of Public Health, and Department of Internal Medicine University of Michigan Medical School Ann Arbor Michigan USA

7. Department of Medicine Weill Medical College of Cornell University New York New York USA

8. Division of Endocrinology, Department of Medicine The University of British Columbia Vancouver British Columbia Canada

9. Department of Medicine Stanford University School of Medicine Palo Alto California USA

Abstract

AbstractAimsDiabetes distress is positively associated with HbA1c and may mediate the relationship between depressive symptoms and HbA1c. This study examined these relationships in a geographically, socioeconomically, and ethnically diverse sample of adults with type 2 diabetes.MethodsUsing data from five US sites evaluating peer support for diabetes management (n = 917), Structural Equation Modeling (SEM) examined whether diabetes distress (four items from Diabetes Distress Scale) mediated the relationship between depressive symptoms (PHQ‐8) and HbA1c. Sites compared interventions of varying content and duration with control conditions. Time from Baseline Assessment to Final Assessment varied from six to 18 months. Site characteristics were controlled by entering site as a covariate along with age, sex, education, diabetes duration, insulin use, and intervention/control assignment.ResultsDepressive symptoms, diabetes distress, and HbA1c were all intercorrelated cross‐sectionally and from Baseline to Final Assessment (rs from 0.10 to 0.57; ps <0.05). In SEM analyses, diabetes distress at Final Assessment mediated the relationship between Baseline depressive symptoms and HbA1c at Final Assessment (indirect effect: b = 0.031, p < 0.001), controlling for Baseline HbA1c and covariates. Parallel analysis of whether depressive symptoms mediated the relationship between Baseline diabetes distress and HbA1c at Final Assessment was not significant.ConclusionsIn this diverse sample, diabetes distress mediated the influence of depressive symptoms on HbA1c but the reverse, depressive symptoms mediating the effect of distress, was not found. These findings add to the evidence that diabetes distress is a worthy intervention target to improve clinical status and quality of life among individuals with type 2 diabetes.

Funder

American Academy of Family Physicians Foundation

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

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