TY - JOUR
T1 - Depression is associated with more aggressive inflammatory bowel disease
AU - Kochar, Bharati
AU - Barnes, Edward L.
AU - Long, Millie D.
AU - Cushing, Kelly C.
AU - Galanko, Joseph
AU - Martin, Christopher F.
AU - Raffals, Laura E.
AU - Sandler, Robert S.
N1 - Funding Information:
Guarantor of the article: Robert S. Sandler, MD, MPH. Specific author contributions: Bharati Kochar: planning and conducting the study, interpreting data, drafting the manuscript, and critical revisions of the manuscript. Edward L. Barnes: interpreting data, drafting the manuscript, and critical revisions of the manuscript. Millie D. Long: planning and conducting the study, collecting the data, interpreting data, and critical revisions of the manuscript. Kelly C. Cushing: interpreting data, and critical revisions of the manuscript. Joseph Galanko: conducting the study, interpreting data, and critical revisions of the manuscript. Christopher F. Martin: collecting the data, conducting the study, interpreting data, and critical revisions of the manuscript. Laura E. Raffals: collecting the data, interpreting data, and critical revisions of the manuscript. Robert S. Sandler: planning and conducting the study, interpreting data, and critical revisions of the manuscript. All authors approved the final manuscript. Financial support: This research was supported by grants from the National Institutes of Health (P30DK034987, T32DK07634, T32DK007130, and UL1TR000448) and by the Helmsley Charitable Trust.
Publisher Copyright:
© 2018 by the American College of Gastroenterology.
PY - 2018
Y1 - 2018
N2 - OBJECTIVES: Depression is prevalent in inflammatory bowel disease (IBD) patients. The impact of depression on IBD is not well-studied. It is unknown how providers should assess depression. METHODS: We used data from the Sinai-Helmsley Alliance for Research Excellence cohort, to assess methods of diagnosing depression and effects of baseline depression on disease activity at follow-up. A patient health questionnaire (PHQ-8) score ≥5 was consistent with mild depression. Relapse was defined as a modified Harvey-Bradshaw Index ≥5 or Simple Clinical Colitis Activity Index >2. We performed binomial regression to calculate adjusted risk ratios (RRs). RESULTS: We included 2,798 Crohn's disease (CD) patients with 22-month mean follow-up and 1,516 ulcerative colitis (UC) patients with 24-month mean follow-up. A total of 64% of CD patients and 45% of UC patients were in remission at baseline. By self-report, 20% of CD and 14% of UC patients were depressed. By PHQ-8, 38% of CD and 32% of UC patients were depressed ( P <0.01). Adjusted for sex, remission, and disease activity, CD patients with baseline depression were at an increased risk for relapse (RR: 2.3; 95% confidence interval (CI): 1.9-2.8), surgery, or hospitalization (RR: 1.3 95% CI: 1.1-1.6) at follow-up. UC patients with baseline depression were also at increased risk for relapse (RR: 1.3; 95% CI: 0.9-1.7), surgery, or hospitalization (RR: 1.3; 95% CI: 1.1-1.5) at follow-up. CONCLUSIONS: Baseline depression is associated with a higher risk for aggressive IBD at follow-up. A single question is not a sensitive method of assessing depression. Providers should consider administering the PHQ-8 to capture those at greater risk for aggressive disease.
AB - OBJECTIVES: Depression is prevalent in inflammatory bowel disease (IBD) patients. The impact of depression on IBD is not well-studied. It is unknown how providers should assess depression. METHODS: We used data from the Sinai-Helmsley Alliance for Research Excellence cohort, to assess methods of diagnosing depression and effects of baseline depression on disease activity at follow-up. A patient health questionnaire (PHQ-8) score ≥5 was consistent with mild depression. Relapse was defined as a modified Harvey-Bradshaw Index ≥5 or Simple Clinical Colitis Activity Index >2. We performed binomial regression to calculate adjusted risk ratios (RRs). RESULTS: We included 2,798 Crohn's disease (CD) patients with 22-month mean follow-up and 1,516 ulcerative colitis (UC) patients with 24-month mean follow-up. A total of 64% of CD patients and 45% of UC patients were in remission at baseline. By self-report, 20% of CD and 14% of UC patients were depressed. By PHQ-8, 38% of CD and 32% of UC patients were depressed ( P <0.01). Adjusted for sex, remission, and disease activity, CD patients with baseline depression were at an increased risk for relapse (RR: 2.3; 95% confidence interval (CI): 1.9-2.8), surgery, or hospitalization (RR: 1.3 95% CI: 1.1-1.6) at follow-up. UC patients with baseline depression were also at increased risk for relapse (RR: 1.3; 95% CI: 0.9-1.7), surgery, or hospitalization (RR: 1.3; 95% CI: 1.1-1.5) at follow-up. CONCLUSIONS: Baseline depression is associated with a higher risk for aggressive IBD at follow-up. A single question is not a sensitive method of assessing depression. Providers should consider administering the PHQ-8 to capture those at greater risk for aggressive disease.
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U2 - 10.1038/ajg.2017.423
DO - 10.1038/ajg.2017.423
M3 - Article
C2 - 29134965
AN - SCOPUS:85047572733
SN - 0002-9270
VL - 113
SP - 80
EP - 85
JO - American Journal of Gastroenterology
JF - American Journal of Gastroenterology
IS - 1
ER -