TY - JOUR
T1 - Characteristics of motor dysfunction in longstanding human immunodeficiency virus
AU - National NeuroAIDS Tissue Consortium
AU - Robinson-Papp, Jessica
AU - Gensler, Gary
AU - Navis, Allison
AU - Sherman, Seth
AU - Ellis, Ronald J.
AU - Gelman, Benjamin B.
AU - Kolson, Dennis L.
AU - Letendre, Scott L.
AU - Singer, Elyse J.
AU - Valdes-Sueiras, Miguel
AU - Morgello, Susan
N1 - Funding Information:
This study was supported by the following National Institutes of Health grants: Manhattan Human Immunodeficiency Virus Brain Bank (grant number U24MH100931); Texas NeuroAIDS Research Center (grant number U24MH100930); National Neurological AIDS Bank (grant number U24MH100929); California NeuroAIDS Tissue Network (grant number U24MH100928); National NeuroAIDS Tissue Consortium Data Coordinating Center (grant number U24MH100925); Motor Dysfunction in Combination Antiretroviral Therapy-Era HIV: Neural Circuitry and Pathogenesis (grant number R01NS108801).
Publisher Copyright:
© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved.
PY - 2020/9/15
Y1 - 2020/9/15
N2 - Background. Cognitive dysfunction in human immunodeficiency virus (HIV) has decreased, but milder forms of HIV-associated neurocognitive disorders (HAND) persist along with motor dysfunction. The HIV Motor Scale (HMS) is a validated tool that captures motor abnormalities on routine neurologic examination and which is associated with cognitive impairment in HIV. In this study, we applied a modified HMS (MHMS) to a nationwide cohort of people with longstanding HIV to characterize and understand the factors contributing to motor dysfunction. Methods. The National NeuroAIDS Tissue Consortium is a nationwide longitudinal cohort study. Participants undergo regular assessments including neurological examination, neuropsychological testing, and immunovirologic data collection. Data from examinations were used to calculate the MHMS score, which was then correlated with history of AIDS-related central nervous system (CNS) disorders (ARCD; eg, prior CNS opportunistic infection), cerebrovascular disease (CVD), and HAND. Results. Sixty-nine percent of participants showed an abnormality on the MHMS, with 27% classified as severe. Results did not vary based on demographic or immunologic variables. The most common abnormalities seen were gait (54%), followed by coordination (39%) and strength (25%), and these commonly co-occurred. CVD (P = .02), history of ARCD (P = .001), and HAND (P = .001) were all associated with higher (ie, worse) HMS in univariate analyses; CVD and ARCD persisted in multivariate analyses. CVD was also marginally associated with symptomatic HAND. Conclusions. Complex motor dysfunction remains common in HIV and is associated with CVD, ARCD, and to a lesser extent, HAND. Future studies are needed to understand the longitudinal trajectory of HIV-associated motor dysfunction, its neural substrates, and impact on quality of life.
AB - Background. Cognitive dysfunction in human immunodeficiency virus (HIV) has decreased, but milder forms of HIV-associated neurocognitive disorders (HAND) persist along with motor dysfunction. The HIV Motor Scale (HMS) is a validated tool that captures motor abnormalities on routine neurologic examination and which is associated with cognitive impairment in HIV. In this study, we applied a modified HMS (MHMS) to a nationwide cohort of people with longstanding HIV to characterize and understand the factors contributing to motor dysfunction. Methods. The National NeuroAIDS Tissue Consortium is a nationwide longitudinal cohort study. Participants undergo regular assessments including neurological examination, neuropsychological testing, and immunovirologic data collection. Data from examinations were used to calculate the MHMS score, which was then correlated with history of AIDS-related central nervous system (CNS) disorders (ARCD; eg, prior CNS opportunistic infection), cerebrovascular disease (CVD), and HAND. Results. Sixty-nine percent of participants showed an abnormality on the MHMS, with 27% classified as severe. Results did not vary based on demographic or immunologic variables. The most common abnormalities seen were gait (54%), followed by coordination (39%) and strength (25%), and these commonly co-occurred. CVD (P = .02), history of ARCD (P = .001), and HAND (P = .001) were all associated with higher (ie, worse) HMS in univariate analyses; CVD and ARCD persisted in multivariate analyses. CVD was also marginally associated with symptomatic HAND. Conclusions. Complex motor dysfunction remains common in HIV and is associated with CVD, ARCD, and to a lesser extent, HAND. Future studies are needed to understand the longitudinal trajectory of HIV-associated motor dysfunction, its neural substrates, and impact on quality of life.
KW - Cerebrovascular disease
KW - HIV
KW - Motor dysfunction
KW - Neurocognitive disorders
UR - http://www.scopus.com/inward/record.url?scp=85090876931&partnerID=8YFLogxK
U2 - 10.1093/cid/ciz986
DO - 10.1093/cid/ciz986
M3 - Article
C2 - 31587032
AN - SCOPUS:85090876931
SN - 1058-4838
VL - 71
SP - 1532
EP - 1538
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 6
ER -