Depression in Adults in the T1D Exchange Clinic Registry
Little is known about the frequency of depression in adults with type 1 diabetes (T1D) or its relationship to diabetes outcomes. The T1D Exchange clinic registry allowed us to explore depression in a large, heterogeneous sample. Participants ≥18 years old (N = 6,172; median age 34 years; median diab...
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Published in | Diabetes care Vol. 37; no. 6; pp. 1563 - 1572 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Alexandria, VA
American Diabetes Association
01.06.2014
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Subjects | |
Online Access | Get full text |
ISSN | 0149-5992 1935-5548 1935-5548 |
DOI | 10.2337/dc13-1867 |
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Abstract | Little is known about the frequency of depression in adults with type 1 diabetes (T1D) or its relationship to diabetes outcomes. The T1D Exchange clinic registry allowed us to explore depression in a large, heterogeneous sample.
Participants ≥18 years old (N = 6,172; median age 34 years; median diabetes duration 16 years; 55% female; and 89% non-Hispanic white) completed the eight-item Patient Health Questionnaire (PHQ-8), a validated, reliable measure of current depression. Probable major depression was defined in four ways: PHQ-8 ≥10, PHQ-8 ≥12, per diagnostic algorithm, and as a continuous variable. Characteristics and clinical outcomes of those with and without depression were compared using logistic and linear regression models.
A total of 4.6-10.3% of participants were classified as probable major depression depending on how defined. Participants classified as depressed were more likely female, nonwhite race/ethnicity, to have a lower household income and lower education level, to exercise less often, to miss insulin doses, and to have one or more complications (neuropathy, nephropathy, treatment for retinopathy, or cardiovascular/cerebrovascular disease) (all P < 0.01). HbA1c was higher in the depressed versus not depressed groups (8.4 ± 1.7% [68 ± 8.6 mmol/mol] vs. 7.8 ± 1.4% [62 ± 15.3 mmol/mol]; P < 0.001). Occurrence of one or more diabetic ketoacidosis events (11 vs. 4%; P < 0.001) and one or more severe hypoglycemic events (18 vs. 9%; P < 0.001) in the past 3 months was higher among depressed participants.
In the T1D Exchange clinic registry, adults with probable major depression have worse clinical outcomes than those not depressed. Whether identification and treatment of depression improves diabetes outcomes requires study. Depression is common in T1D, and better identification and treatment of this comorbid condition is needed. |
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AbstractList | Little is known about the frequency of depression in adults with type 1 diabetes (T1D) or its relationship to diabetes outcomes. The T1D Exchange clinic registry allowed us to explore depression in a large, heterogeneous sample.OBJECTIVELittle is known about the frequency of depression in adults with type 1 diabetes (T1D) or its relationship to diabetes outcomes. The T1D Exchange clinic registry allowed us to explore depression in a large, heterogeneous sample.Participants ≥18 years old (N = 6,172; median age 34 years; median diabetes duration 16 years; 55% female; and 89% non-Hispanic white) completed the eight-item Patient Health Questionnaire (PHQ-8), a validated, reliable measure of current depression. Probable major depression was defined in four ways: PHQ-8 ≥10, PHQ-8 ≥12, per diagnostic algorithm, and as a continuous variable. Characteristics and clinical outcomes of those with and without depression were compared using logistic and linear regression models.RESEARCH DESIGN AND METHODSParticipants ≥18 years old (N = 6,172; median age 34 years; median diabetes duration 16 years; 55% female; and 89% non-Hispanic white) completed the eight-item Patient Health Questionnaire (PHQ-8), a validated, reliable measure of current depression. Probable major depression was defined in four ways: PHQ-8 ≥10, PHQ-8 ≥12, per diagnostic algorithm, and as a continuous variable. Characteristics and clinical outcomes of those with and without depression were compared using logistic and linear regression models.A total of 4.6-10.3% of participants were classified as probable major depression depending on how defined. Participants classified as depressed were more likely female, nonwhite race/ethnicity, to have a lower household income and lower education level, to exercise less often, to miss insulin doses, and to have one or more complications (neuropathy, nephropathy, treatment for retinopathy, or cardiovascular/cerebrovascular disease) (all P < 0.01). HbA1c was higher in the depressed versus not depressed groups (8.4 ± 1.7% [68 ± 8.6 mmol/mol] vs. 7.8 ± 1.4% [62 ± 15.3 mmol/mol]; P < 0.001). Occurrence of one or more diabetic ketoacidosis events (11 vs. 4%; P < 0.001) and one or more severe hypoglycemic events (18 vs. 9%; P < 0.001) in the past 3 months was higher among depressed participants.RESULTSA total of 4.6-10.3% of participants were classified as probable major depression depending on how defined. Participants classified as depressed were more likely female, nonwhite race/ethnicity, to have a lower household income and lower education level, to exercise less often, to miss insulin doses, and to have one or more complications (neuropathy, nephropathy, treatment for retinopathy, or cardiovascular/cerebrovascular disease) (all P < 0.01). HbA1c was higher in the depressed versus not depressed groups (8.4 ± 1.7% [68 ± 8.6 mmol/mol] vs. 7.8 ± 1.4% [62 ± 15.3 mmol/mol]; P < 0.001). Occurrence of one or more diabetic ketoacidosis events (11 vs. 4%; P < 0.001) and one or more severe hypoglycemic events (18 vs. 9%; P < 0.001) in the past 3 months was higher among depressed participants.In the T1D Exchange clinic registry, adults with probable major depression have worse clinical outcomes than those not depressed. Whether identification and treatment of depression improves diabetes outcomes requires study. Depression is common in T1D, and better identification and treatment of this comorbid condition is needed.CONCLUSIONSIn the T1D Exchange clinic registry, adults with probable major depression have worse clinical outcomes than those not depressed. Whether identification and treatment of depression improves diabetes outcomes requires study. Depression is common in T1D, and better identification and treatment of this comorbid condition is needed. Little is known about the frequency of depression in adults with type 1 diabetes (T1D) or its relationship to diabetes outcomes. The T1D Exchange clinic registry allowed us to explore depression in a large, heterogeneous sample. Participants ≥18 years old (N = 6,172; median age 34 years; median diabetes duration 16 years; 55% female; and 89% non-Hispanic white) completed the eight-item Patient Health Questionnaire (PHQ-8), a validated, reliable measure of current depression. Probable major depression was defined in four ways: PHQ-8 ≥10, PHQ-8 ≥12, per diagnostic algorithm, and as a continuous variable. Characteristics and clinical outcomes of those with and without depression were compared using logistic and linear regression models. A total of 4.6-10.3% of participants were classified as probable major depression depending on how defined. Participants classified as depressed were more likely female, nonwhite race/ethnicity, to have a lower household income and lower education level, to exercise less often, to miss insulin doses, and to have one or more complications (neuropathy, nephropathy, treatment for retinopathy, or cardiovascular/cerebrovascular disease) (all P < 0.01). HbA1c was higher in the depressed versus not depressed groups (8.4 ± 1.7% [68 ± 8.6 mmol/mol] vs. 7.8 ± 1.4% [62 ± 15.3 mmol/mol]; P < 0.001). Occurrence of one or more diabetic ketoacidosis events (11 vs. 4%; P < 0.001) and one or more severe hypoglycemic events (18 vs. 9%; P < 0.001) in the past 3 months was higher among depressed participants. In the T1D Exchange clinic registry, adults with probable major depression have worse clinical outcomes than those not depressed. Whether identification and treatment of depression improves diabetes outcomes requires study. Depression is common in T1D, and better identification and treatment of this comorbid condition is needed. Little is known about the frequency of depression in adults with type 1 diabetes (T1D) or its relationship to diabetes outcomes. The T1D Exchange clinic registry allowed us to explore depression in a large, heterogeneous sample. Participants ≥18 years old (N = 6,172; median age 34 years; median diabetes duration 16 years; 55% female; and 89% non-Hispanic white) completed the eight-item Patient Health Questionnaire (PHQ-8), a validated, reliable measure of current depression. Probable major depression was defined in four ways: PHQ-8 ≥10, PHQ-8 ≥12, per diagnostic algorithm, and as a continuous variable. Characteristics and clinical outcomes of those with and without depression were compared using logistic and linear regression models. A total of 4.6-10.3% of participants were classified as probable major depression depending on how defined. Participants classified as depressed were more likely female, nonwhite race/ethnicity, to have a lower household income and lower education level, to exercise less often, to miss insulin doses, and to have one or more complications (neuropathy, nephropathy, treatment for retinopathy, or cardiovascular/cerebrovascular disease) (all P < 0.01). HbA1c was higher in the depressed versus not depressed groups (8.4 ± 1.7% [68 ± 8.6 mmol/mol] vs. 7.8 ± 1.4% [62 ± 15.3 mmol/mol]; P < 0.001). Occurrence of one or more diabetic ketoacidosis events (11 vs. 4%; P < 0.001) and one or more severe hypoglycemic events (18 vs. 9%; P < 0.001) in the past 3 months was higher among depressed participants. In the T1D Exchange clinic registry, adults with probable major depression have worse clinical outcomes than those not depressed. Whether identification and treatment of depression improves diabetes outcomes requires study. Depression is common in T1D, and better identification and treatment of this comorbid condition is needed. |
Author | Olson, Beth A. Young, Laura A. Weinstock, Ruth S. Foster, Nicole C. Xing, Dongyuan Bergenstal, Richard M. Kittelsrud, Julie M. Peters, Anne L. Maahs, David M. Trief, Paula M. Beck, Roy W. Miller, Kellee M. |
Author_xml | – sequence: 1 givenname: Paula M. surname: Trief fullname: Trief, Paula M. organization: Endocrinology, Diabetes, and Metabolism, Department of Medicine, State University of New York Upstate Medical University, Syracuse, NY – sequence: 2 givenname: Dongyuan surname: Xing fullname: Xing, Dongyuan organization: Jaeb Center for Health Research, Tampa, FL – sequence: 3 givenname: Nicole C. surname: Foster fullname: Foster, Nicole C. organization: Jaeb Center for Health Research, Tampa, FL – sequence: 4 givenname: David M. surname: Maahs fullname: Maahs, David M. organization: Barbara Davis Center for Childhood Diabetes, Aurora, CO – sequence: 5 givenname: Julie M. surname: Kittelsrud fullname: Kittelsrud, Julie M. organization: Avera McKennan Hospital & University Health Center, Sioux Falls, SD – sequence: 6 givenname: Beth A. surname: Olson fullname: Olson, Beth A. organization: Park Nicollet International Diabetes Center, Minneapolis, MN – sequence: 7 givenname: Laura A. surname: Young fullname: Young, Laura A. organization: Diabetes Center for Research, School of Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, NC – sequence: 8 givenname: Anne L. surname: Peters fullname: Peters, Anne L. organization: Keck School of Medicine of USC, Los Angeles, CA – sequence: 9 givenname: Richard M. surname: Bergenstal fullname: Bergenstal, Richard M. organization: Park Nicollet International Diabetes Center, Minneapolis, MN – sequence: 10 givenname: Kellee M. surname: Miller fullname: Miller, Kellee M. organization: Jaeb Center for Health Research, Tampa, FL – sequence: 11 givenname: Roy W. surname: Beck fullname: Beck, Roy W. organization: Jaeb Center for Health Research, Tampa, FL – sequence: 12 givenname: Ruth S. surname: Weinstock fullname: Weinstock, Ruth S. organization: Endocrinology, Diabetes, and Metabolism, Department of Medicine, State University of New York Upstate Medical University, Syracuse, NY |
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Snippet | Little is known about the frequency of depression in adults with type 1 diabetes (T1D) or its relationship to diabetes outcomes. The T1D Exchange clinic... |
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SubjectTerms | Adolescent Adult Adult and adolescent clinical studies Aged Aged, 80 and over Biological and medical sciences Clinical outcomes Depression Depressive Disorder - diagnosis Depressive Disorder - etiology Depressive Disorder - psychology Diabetes Diabetes Mellitus, Type 1 - complications Diabetes Mellitus, Type 1 - psychology Diabetes. Impaired glucose tolerance Diabetic Ketoacidosis - diagnosis Diabetic Ketoacidosis - epidemiology Diabetic Ketoacidosis - psychology Endocrine pancreas. Apud cells (diseases) Endocrinopathies Ethnic Groups Ethnicity Female Humans Hypoglycemia Hypoglycemia - diagnosis Hypoglycemia - epidemiology Hypoglycemia - psychology Male Medical sciences Mental depression Metabolic diseases Middle Aged Mood disorders Outpatient Clinics, Hospital - statistics & numerical data Prevalence Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Registries Regression analysis United States - epidemiology Young Adult |
Title | Depression in Adults in the T1D Exchange Clinic Registry |
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