Comorbidity of bipolar disorder and substance abuse in Costa Rica: pedigree- and population-based studies

被引:13
作者
Escamilla, MA
Batki, S
Reus, VI
Spesny, M
Molina, J
Service, S
Vinogradov, S
Neylan, T
Mathews, C
Meza, L
Gallegos, A
Montero, AP
Cruz, ML
Neuhaus, J
Roche, E
Smith, L
Leon, P
Freimer, NB
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Psychiat, San Antonio, TX 78229 USA
[2] San Francisco Gen Hosp, Neurogenet Lab, San Francisco, CA 94110 USA
[3] San Francisco Gen Hosp, Ctr Neurobiol & Psychiat, San Francisco, CA 94110 USA
[4] SUNY Upstate Med Ctr, Dept Psychiat, Syracuse, NY USA
[5] Vet Adm Med Ctr, Dept Psychiat, San Francisco, CA 94121 USA
[6] Univ Calif San Francisco, Dept Psychiat, San Francisco, CA 94143 USA
[7] Univ Costa Rica, Cell & Mol Biol Res Ctr, San Jose, Costa Rica
[8] Univ Costa Rica, Escuela Med, San Jose, Costa Rica
[9] Hosp Calderon Guardia, San Jose, Costa Rica
[10] Univ Calif San Francisco, Dept Epidemiol, San Francisco, CA 94143 USA
关键词
bipolar disorder; genetics; substance abuse; alcoholism;
D O I
10.1016/S0165-0327(01)00373-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The purpose of this study was to determine the prevalence of substance use disorders (substance abuse or substance dependence: SA/SD) in a large sample of Bipolar Type I (BPI) patients drawn from the Costa Rican population and to describe the effects of SA/SD on the course of their bipolar disorder. Method: 110 subjects from two high-risk (for BPI) Costa Rican pedigrees and 205 unrelated Costa Rican BPI subjects were assessed using structured interviews and a best estimate process. chi(2) and survival analyses were performed to assess the effect of gender on comorbidity risk, and the effect of comorbidity on the clinical course of BPI. Results: SA/SD (primarily alcohol dependence) occurred in 17% of the BPI patients from the population sample and 35% of the BPI patients from the pedigree sample. Comorbid SA/SD was strongly associated with gender chi(2) = 16.84, P = 0.00004). In comorbid subjects, alcohol dependence tended to predate the first manic episode (chi(2) = 6.54, P < 0.025). History of SA/SD did not significantly alter the prevalence of psychosis or age of onset of mania in BPI subjects. Conclusions: These results suggest that SA/SD comorbidity rates are lower in this type of population than in BPI patient populations in the US. Gender is a strong predictor of comorbidity prevalence in BPI patients from this population. Although SA/SD may be a risk factor for precipitating BPI in those at risk, in this population comorbid BPI subjects do not have a different onset or course of BPI in comparison to BPI patients without comorbidity. (C) 2002 Elsevier Science B V All rights reserved.
引用
收藏
页码:71 / 83
页数:13
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