TY - JOUR
T1 - Increased depression risk among patients with chronic osteomyelitis
AU - Tseng, Chun Hung
AU - Huang, Wei Shih
AU - Muo, Chih Hsin
AU - Chang, Yen Jung
AU - Kao, Chia Hung
N1 - Publisher Copyright:
© 2014 Elsevier Inc.
PY - 2014/12/1
Y1 - 2014/12/1
N2 - Objective: Inflammatory processes, which provoke alternations of neurotransmitter metabolism, neuroendocrine function, and neuroplasticity in the brain, might promote depression. In depression patients who do not exhibit risk factors, including hypertension, diabetes, coronary heart disease, stroke, Parkinson's disease and dementia, particularly in young people, inflammation is a likely risk factor for depression. We explored whether chronic osteomyelitis (COM), a chronic inflammatory disease, increases depression risk. Methods: A Taiwanese national insurance claims data set of more than 22 million enrollees was used to select 15,529 COM patients without depression history and 62,116 randomly selected age- and gender-matched controls without depression and COM history to trace depression development for an 12-year follow-up period from January 1, 1999 to December 31, 2010. The depression risk was analyzed using the Cox proportional hazards regression model. Results: The above-mentioned risk factors for depression were more frequent in the COM cohort, who exhibited significantly higher depression risk than the control group did. Comparing only those without comorbidities, the COM group exhibited higher depression risk than the control group did (hazard ratio [HR] = 3.04, 95% confidence interval [CI]: 2.55-3.62). The younger population carried even greater risk (age < 45: HR = 6.08, 95% CI: 1.71-7.85; age > 65: HR = 1.75, 95% CI: 1.39-2.19). Conclusions: This is the first study connecting COM to increased risk of developing depression. The outcomes suggest that COM is a substantial depression predictor and call for a closer focus on these patients for more rigorous depression prevention, particularly in young people.
AB - Objective: Inflammatory processes, which provoke alternations of neurotransmitter metabolism, neuroendocrine function, and neuroplasticity in the brain, might promote depression. In depression patients who do not exhibit risk factors, including hypertension, diabetes, coronary heart disease, stroke, Parkinson's disease and dementia, particularly in young people, inflammation is a likely risk factor for depression. We explored whether chronic osteomyelitis (COM), a chronic inflammatory disease, increases depression risk. Methods: A Taiwanese national insurance claims data set of more than 22 million enrollees was used to select 15,529 COM patients without depression history and 62,116 randomly selected age- and gender-matched controls without depression and COM history to trace depression development for an 12-year follow-up period from January 1, 1999 to December 31, 2010. The depression risk was analyzed using the Cox proportional hazards regression model. Results: The above-mentioned risk factors for depression were more frequent in the COM cohort, who exhibited significantly higher depression risk than the control group did. Comparing only those without comorbidities, the COM group exhibited higher depression risk than the control group did (hazard ratio [HR] = 3.04, 95% confidence interval [CI]: 2.55-3.62). The younger population carried even greater risk (age < 45: HR = 6.08, 95% CI: 1.71-7.85; age > 65: HR = 1.75, 95% CI: 1.39-2.19). Conclusions: This is the first study connecting COM to increased risk of developing depression. The outcomes suggest that COM is a substantial depression predictor and call for a closer focus on these patients for more rigorous depression prevention, particularly in young people.
KW - Chronic osteomyelitis
KW - Depression
KW - Inflammation
UR - http://www.scopus.com/inward/record.url?scp=84919397974&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84919397974&partnerID=8YFLogxK
U2 - 10.1016/j.jpsychores.2014.09.008
DO - 10.1016/j.jpsychores.2014.09.008
M3 - Article
C2 - 25258357
AN - SCOPUS:84919397974
SN - 0022-3999
VL - 77
SP - 535
EP - 540
JO - Journal of Psychosomatic Research
JF - Journal of Psychosomatic Research
IS - 6
ER -