4.5 Article

HIV and Chronic Methamphetamine Dependence Affect Cerebral Blood Flow

Journal

JOURNAL OF NEUROIMMUNE PHARMACOLOGY
Volume 6, Issue 3, Pages 409-419

Publisher

SPRINGER
DOI: 10.1007/s11481-011-9270-y

Keywords

Human immunodeficiency virus; Methamphetamine; Cerebral blood flow; Lenticular nuclei; Highly active antiretroviral therapy

Funding

  1. Dana Foundation [DF3857-41880]
  2. NIH [1K23MH081786, 1R01NR012657, NS-36722, NS-42069, MH22005, AI47033, P30 MH62512, P01 DA12065]

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Human immunodeficiency virus (HIV) and methamphetamine (METH) dependence are independently associated with neuronal dysfunction. The coupling between cerebral blood flow (CBF) and neuronal activity is the basis of many task-based functional neuroimaging techniques. We examined the interaction between HIV infection and a previous history of METH dependence on CBF within the lenticular nuclei (LN). Twenty-four HIV-/METH-, eight HIV-/METH+, 24 HIV+/METH-, and 15 HIV+/METH+ participants performed a finger tapping paradigm. A multiple regression analysis of covariance assessed associations and two-way interactions between CBF and HIV serostatus and/or previous history of METH dependence. HIV+ individuals had a trend towards a lower baseline CBF (-10%, p = 0.07) and greater CBF changes for the functional task (+32%, p = 0.01) than HIV- subjects. Individuals with a previous history of METH dependence had a lower baseline CBF (-16%, p = 0.007) and greater CBF changes for a functional task (+33%, p = 0.02). However, no interaction existed between HIV serostatus and previous history of METH dependence for either baseline CBF (p = 0.53) or CBF changes for a functional task (p = 0.10). In addition, CBF and volume in the LN were not correlated. A possible additive relationship could exist between HIV infection and a history of METH dependence on CBF with a previous history of METH dependence having a larger contribution. Abnormalities in CBF could serve as a surrogate measure for assessing the chronic effects of HIV and previous METH dependence on brain function.

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