Association of Antidepressant Medications With Incident Type 2 Diabetes Among Medicaid-Insured Youths

被引:37
|
作者
Burcu, Mehmet [1 ]
Zito, Julie M. [1 ,2 ]
Safer, Daniel J. [3 ,4 ]
Magder, Laurence S. [5 ]
dosReis, Susan [1 ]
Shaya, Fadia T. [1 ]
Rosenthal, Geoffrey L. [5 ,6 ]
机构
[1] Univ Maryland, Dept Pharmaceut Hlth Serv Res, 220 Arch St, Baltimore, MD 21201 USA
[2] Univ Maryland, Dept Psychiat, Baltimore, MD 21201 USA
[3] Johns Hopkins Med Inst, Dept Pediat, Baltimore, MD 21205 USA
[4] Johns Hopkins Med Inst, Dept Psychiat, Baltimore, MD 21205 USA
[5] Univ Maryland, Dept Epidemiol & Publ Hlth, Baltimore, MD 21201 USA
[6] Univ Maryland, Dept Pediat, Baltimore, MD 21201 USA
关键词
DISEASE RISK SCORES; SEROTONIN REUPTAKE INHIBITORS; MENTAL-HEALTH-CARE; PREVENTION PROGRAM; MEDICINE USE; CHILDREN; MELLITUS; ADOLESCENTS; TRENDS; DEPRESSION;
D O I
10.1001/jamapediatrics.2017.2896
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
IMPORTANCE Antidepressants are one of the most commonly prescribed classes of psychotropic medications among US youths. For adults, there is emerging evidence on the increased risk of type 2 diabetes in association with antidepressant use. However, little is known about the antidepressant treatment-emergent risk of type 2 diabetes among youths. OBJECTIVE To assess the association between antidepressant use and the risk of incident type 2 diabetes in youths by antidepressant subclass and according to duration of use, cumulative dose, and average daily dose. DESIGN, SETTING, AND PARTICIPANTS A retrospective cohort study was conducted using Medicaid claims data from 4 geographically diverse, large states of youths 5 to 20 years of age who initiated antidepressant treatment from January 1, 2005, to December 31, 2009. EXPOSURES Antidepressant use (selective serotonin reuptake inhibitors [SSRIs] or serotonin-norepinephrine reuptake inhibitors [SNRIs], tricyclic or other cyclic antidepressants, and other antidepressants) was assessed using the following 4 time-varying measures: current or former use, duration of use, cumulative dose, and average daily dose. MAIN OUTCOMES AND MEASURES Incident type 2 diabeteswas assessed using discrete-time failure models, adjusting for disease risk score estimated using more than 125 baseline and time-dependent covariates. RESULTS In this cohort of 119 608 youths aged 5 to 20 years who initiated antidepressant treatment (59 087 female youths and 60 521 male youths; 54.7% between 5 and 14 years of age) with a mean follow-up of 22.8 months, 79 285 [66.3%] had SSRI or SNRI exposure. The risk of type 2 diabetes was significantly greater during current use than former use of SSRIs or SNRIs (absolute risk, 1.29 per 10 000 person-months vs 0.64 per 10 000 person-months; adjusted relative risk [RR], 1.88; 95% CI, 1.34-2.64) and tricyclic or other cyclic antidepressants (absolute risk, 0.89 per 10 000 person-months vs 0.48 per 10 000 person-months; RR, 2.15; 95% CI, 1.06-4.36), but not of other antidepressants (absolute risk, 1.15 per 10 000 person-months vs 1.12 per 10 000 person-months; RR, 0.99; 95% CI, 0.66-1.50). Furthermore, for youths currently using SSRIs or SNRIs, the risk of type 2 diabetes increased with the duration of use (RR, 2.66; 95% CI, 1.45-4.88 for > 210 days and RR, 2.56; 95% CI, 1.29-5.08 for 151-210 days compared with 1-90 days) and with the cumulative dose (RR, 2.44; 95% CI, 1.35-4.43 for > 4500mg and RR, 2.17; 95% CI, 1.07-4.40 for 3001-4500mg compared with 1-1500mg in fluoxetine hydrochloride dose equivalents). By contrast, neither the duration nor the cumulative dose of other antidepressants was associated with an increased risk of type 2 diabetes. The risk of type 2 diabetes increased significantly with the average daily dose among youths with more than 150 days of SSRI or SNRI use (RR, 2.39; 95% CI, 1.04-5.52 for >15.0 vs <15.0mg/d) but not among youths with 1 to 150 days of SSRI or SNRI use. CONCLUSIONS AND RELEVANCE In a large cohort of youths insured by Medicaid, the use of SSRIs or SNRIs-the most commonly used antidepressant subclass-was associated with an increased risk of type 2 diabetes that intensified with increasing duration of use, cumulative dose, and average daily dose.
引用
收藏
页码:1200 / 1207
页数:8
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