The association between benzodiazepine use and greater risk of neurocognitive impairment is moderated by medical burden in people with HIV

被引:8
作者
Sundermann, Erin E. [1 ]
Saloner, Rowan [1 ,2 ,3 ]
Rubtsova, Anna [4 ]
Nguyen, Annie L. [5 ]
Letendre, Scott [1 ,6 ]
Moore, Raeanne C. [1 ]
Cherner, Mariana [1 ]
Ma, Qing [7 ]
Marquine, Maria J. [1 ,6 ]
机构
[1] Univ Calif San Diego, Dept Psychiat, 220 Dickinson St B, San Diego, CA 92103 USA
[2] Univ Calif San Diego, San Diego State Univ, Joint Doctoral Program Clin Psychol, San Diego, CA 92103 USA
[3] Univ Calif San Francisco, Dept Neurol, 505 Parnassus Ave, San Francisco, CA 94143 USA
[4] Emory Univ, Rollins Sch Publ Hlth, Dept Behav Social & Hlth Educ Sci, 1518 Clifton Rd, Atlanta, GA 30322 USA
[5] Univ Southern Calif, Keck Sch Med, Dept Family Med, 1975 Zonal Ave, Los Angeles, CA 90033 USA
[6] Univ Calif San Diego, Dept Med, 220 Dickinson St B, San Diego, CA 92103 USA
[7] Univ Buffalo, Dept Pharm Practice, 285 Pharm Bldg Buffalo, New York, NY 14214 USA
关键词
Benzodiazepines; HIV; Neurocognitive impairment; Comorbidities; Medical burden; VETERANS AGING COHORT; COGNITIVE FUNCTION; DEFICIT SCORES; INFECTION; DEMENTIA; DECLINE; INDEX; BRAIN; INFLAMMATION; DISORDERS;
D O I
10.1007/s13365-022-01076-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Benzodiazepine use is linked to neurocognitive impairment (NCI) in the general population and people with HIV (PWH); however, this relationship may depend on age-related factors such as medical comorbidities, which occur at an elevated rate and manifest earlier in PWH. We retrospectively examined whether chronological age or medical burden, a clinical marker for aging, moderated the relationship between benzodiazepine use and NCI in PWH. Participants were 435 PWH on antiretroviral therapy who underwent neurocognitive and medical evaluations, including self-reported current benzodiazepine use. A medical burden index score (proportion of accumulated multisystem deficits) was calculated from 28 medical deficits. Demographically corrected cognitive deficit scores from 15 neuropsychological tests were used to calculate global and domain-specific NCI based on established cut-offs. Logistic regressions separately modeled global and domain-specific NCI as a function of benzodiazepine x age and benzodiazepine x medical burden interactions, adjusting for current affective symptoms and HIV disease characteristics. A statistically significant benzodiazepine x medical burden interaction (p = .006) revealed that current benzodiazepine use increased odds of global NCI only among those who had a high medical burden (index score > 0.3 as indicated by the Johnson-Neyman analysis), which was driven by the domains of processing speed, motor, and verbal fluency. No age x benzodiazepine interactive effects on NCI were present. Findings suggest that the relationship between BZD use and NCI among PWH is specific to those with greater medical burden, which may be a greater risk factor for BZD-related NCI than chronological age.
引用
收藏
页码:410 / 421
页数:12
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