Risk of developing diabetes mellitus and hyperlipidemia among patients with bipolar disorder, major depressive disorder, and schizophrenia: A 10-year nationwide population-based prospective cohort study

被引:58
作者
Bai, Ya-Mei [1 ,2 ]
Su, Tung-Ping [1 ,2 ]
Chen, Mu-Hong [1 ]
Chen, Tzeng-Ji [3 ,4 ]
Chang, Wen-Han [1 ]
机构
[1] Taipei Vet Gen Hosp, Dept Psychiat, Taipei, Taiwan
[2] Natl Yang Ming Univ, Coll Med, Dept Psychiat, Taipei 11217, Taiwan
[3] Taipei Vet Gen Hosp, Dept Family Med, Taipei, Taiwan
[4] Natl Yang Ming Univ, Dept Family Med, Coll Med, Taipei 11217, Taiwan
关键词
Bipolar disorder; Major depressive disorder; Schizophrenia; Diabetes mellitus; Hyperlipidemia; METABOLIC SYNDROME; BODY-WEIGHT; ASSOCIATION; SYMPTOMS; OBESITY; LITHIUM; GAIN; RISPERIDONE; TOPIRAMATE; MANAGEMENT;
D O I
10.1016/j.jad.2013.02.019
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Background: The high comorbidity of metabolic side effects with severe mental disorders (SMDs), including bipolar disorder (BD), major depressive disorder (MDD), and schizophrenia, had gained much attention, because the excess mortality of these patients is mainly due to physical illness. However, most of these studies were with cross-sectional study design, the time course of metabolic side effects and SMD cannot be elucidated without a cohort study. Method: Using a nationwide database with a large sample size and a matched control cohort study design, we enrolled patients with SMDs but without diagnoses of and medications for DM and hyperlipidemia from 1996 to 2000, and followed them to the end of 2010. We compared them with age and gender-matched controls (1:4) for the incidence of DM and hyperlipidemia. Results: The identified cases were 367 patients with BD, 417 patients with MDD, and 1993 patients with schizophrenia, with average age of 45.3 +/- 14.0, 46.5 +/- 13.7, and 45.9 +/- 12.3, respectively. The patients with BD and schizophrenia had increased risk of initiation of anti-diabetic medications (10.1% vs. 6.3%, p=0.012; 13.3% vs. 7.2% p < 0.001; respectively), and anti-hyperlipidemia medications (15.8% vs.10.5%, p=0.004; 14.2% vs.12.1%, p=0.005; respectively) than the controls. After controlling age, gender, urbanization, and income, the Cox regression model showed significantly increased risk of initiation of anti-diabetic medications among patients with BD (hazard ratio (HR) of 1.702, 95% confidence interval (CI): 1.155-2.507) and schizophrenia (HR of 1.793, 95% CI: 1.532-2.098). Increased risk of initiation of anti-hyperlipidemia medications was also noted among patients with BD (HR of 1.506, 95% CI: 1.107-2.047) and schizophrenia (HR of 1.154, 95% CI: 1.002-1.329). The patients with MDD did not show increased risk of initiation of these medications than the controls. Conclusions: This first 10-year nationwide population-based prospective matched control cohort study showed increased risks of initiation of anti-diabetic and anti-hyperlipidemia medications among patients with BD and schizophrenia. No significant increased risk was noted among the patients with MDD. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:57 / 62
页数:6
相关论文
共 52 条
[1]
Diabetes mellitus and comorbid depression: improvement of both diseases with milnacipran. A replication study (results of the Austrian Major Depression Diabetes Mellitus study group) [J].
Abrahamian, Heidemarie ;
Hofmann, Peter ;
Kinzl, Johann ;
Toplak, Hermann .
NEUROPSYCHIATRIC DISEASE AND TREATMENT, 2012, 8 :355-360
[3]
Depressive symptoms and risk of type 2 diabetes in women [J].
Arroyo, C ;
Hu, FB ;
Ryan, LM ;
Kawachi, I ;
Colditz, GA ;
Speizer, FE ;
Manson, J .
DIABETES CARE, 2004, 27 (01) :129-133
[4]
Association of Weight Gain and Metabolic Syndrome in Patients Taking Clozapine: An 8-Year Cohort Study [J].
Bai, Ya Mei ;
Lin, Chao-Cheng ;
Chen, Jen-Yeu ;
Chen, Tzu Ting ;
Su, Tung-Pine ;
Chou, Pesus .
JOURNAL OF CLINICAL PSYCHIATRY, 2011, 72 (06) :751-756
[5]
Obesity and related metabolic abnormalities during antipsychotic drug administration: Mechanisms, management and research perspectives [J].
Baptista, T ;
Kin, NMKNY ;
Beaulieu, S ;
de Baptista, EA .
PHARMACOPSYCHIATRY, 2002, 35 (06) :205-219
[6]
Causes of the excess mortality of schizophrenia [J].
Brown, S ;
Inskip, H ;
Barraclough, B .
BRITISH JOURNAL OF PSYCHIATRY, 2000, 177 :212-217
[7]
Severe hyperlipidemia associated with olanzapine and quetiapine use [J].
Carnahan, Ryan M. ;
Reantaso, Antonio A. ;
Teegarden, Beth A. ;
Pogue, Todd .
AMERICAN JOURNAL OF PSYCHIATRY, 2007, 164 (10) :1614-1615
[8]
Depression and late mortality after myocardial infarction in the Enhancing Recovery in Coronary Heart Disease (ENRICHD) study [J].
Carney, RM ;
Blumenthal, JA ;
Freedland, KE ;
Youngblood, M ;
Veith, RC ;
Burg, MM ;
Cornell, C ;
Saab, PG ;
Kaufmann, PG ;
Czajkowski, SM ;
Jaffe, AS .
PSYCHOSOMATIC MEDICINE, 2004, 66 (04) :466-474
[9]
Depression, heart rate variability, and acute myocardial infarction [J].
Carney, RM ;
Blumenthal, JA ;
Stein, PK ;
Watkins, L ;
Catellier, D ;
Berkman, LF ;
Czajkowski, SM ;
O'Connor, C ;
Stone, PH ;
Freedland, KE .
CIRCULATION, 2001, 104 (17) :2024-2028
[10]
Casey DE, 2001, J CLIN PSYCHIAT, V62, P4