TY - JOUR
T1 - Distal sensory peripheral neuropathy in human immunodeficiency virus type 1-positive individuals before and after antiretroviral therapy initiation in diverse resource-limited settings
AU - AIDS Clinical Trials Group 5199 and 5271 study team
AU - Vecchio, Alyssa C.
AU - Marra, Christina M.
AU - Schouten, Jeffrey
AU - Jiang, Hongyu
AU - Kumwenda, Johnstone
AU - Supparatpinyo, Khuanchai
AU - Hakim, James
AU - Sacktor, Ned
AU - Campbell, Thomas B.
AU - Tripathy, Srikanth
AU - Kumarasamy, Nagalingeswaran
AU - Rosa, Alberto La
AU - Santos, Breno
AU - Silva, Marcus T.
AU - Kanyama, Cecilia
AU - Firnhaber, Cindy
AU - Hosseinipour, Mina C.
AU - Mngqibisa, Rosie
AU - Hall, Colin
AU - Cinque, Paola
AU - Robertson, Kevin
N1 - Funding Information:
The project described was supported by the NIMH and the AIDS Clinical Trials Group funded by the NIAID (award U01AI068636) and by the Statistical and Data Analysis Center (grant AI-068634). Thomas Campbell (grant support from NIAID AIDS Clinical Trail Unit [CTU], AI069450). Deise Vieira and Marcus Tulius T Silva (National Institute of Infectolgy-Oswaldo Cruz Foundation [IPECFIOCRUZ]; site 12101; CTU grant AI69476). Umesh Lalloo and Rosie Mngqibisa (Durban Adult HIV clinical research site [HIV CRS]; site 11201; CTU grant 5U01AI069426-03). Nagalingeshwaran Kumarasamy and Jabin Sharma (YRGCARE Medical Centre; site 11701; CTU grant AI069432). Virginia M. Kayoyo and Charity Potani (Franklin Kilembe University of North Carolina Project, Kamuzu Central Hospital, Lilongwe; site 12001; CTU grant AI069518). Mauleen Waison and Rachel Mahachi-Parirenyatwa (CRS; site 30313; CTU grant BRS-ACURE-Q-08-00173-TOOI-OOO). Cynthia Firnhaber, Sharla Faesen, and Daphne S. Radebe (Wits HIV Clinical Research Site; Helen Joseph Hospital; site 11101; CTU grant AI069463; BRS-ACURE-Q-07-00143 T006). Thira Sirisanthana and Daralak Tavornprasit (Research Institute for Health Sciences-Chiang Mai University; site 11501; CTU grant AI069399; AACTG.27.5199.06). Maria Siliprandiand Renata Londero (Hospital Nossa Senhora da Conceicao CRS; site 12201; CTU grant 5 U01 AI069401). Anjali A. Joglekar and Srikanth Prasad Tripathy (NARI Pune CRS; site 11601; CTU grant 5U01AI069417-03). Ben Kalonga and Henry Chamba (College of Medicine-Johns Hopkins Project; site 30301; CTU grant U01A1069518). Carlos Mosquera and Rosa Infante (INMENSA-Lince CRS; site 11302; CTU grant 5U01 AI069438-03; BRS- ACURE-Q-07-00141-T001-001). Jorge Sanchez and Juan Carlos Hurtado (Asociación Civil Impacta Salud y Educación; site 11301; CTU grant AI069438; BRS-ACURE-Q-08-00007-T-002). Manisha V. Ghate and Madhura Nene (NARI-NIV Clinic; site 11603; CTU grant 5U01AI069417-03). Raman Gnagakhedkar and Usha Katti (Dr Kotnis Dispensary, NARI; site 11602; CTU grant 5U01AI069417-03). H. J. was funded in part by the Statistical and Data Management Center of the Adult AIDS Clinical Trials Group (grant 1 U01 068634). J. S. received grant support from NIAID (CTU UM1 AI06948-08). Names of AIDS Clinical Trials Group 5199 and 5271 team members who received grant funding to carry out the clinical trial are included in acknowledgement, but since they did not participate in the neuropathy analysis and manuscript writing they where not listed as name authors.
Publisher Copyright:
© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved.
PY - 2020/7/1
Y1 - 2020/7/1
N2 - Background. Distal sensory peripheral neuropathy (DSPN) is a complication of human immunodeficiency virus (HIV). We estimate DSPN prevalence in 7 resource-limited settings (RLSs) for combination antiretroviral therapy (cART)-naive people living with HIV (PLWH) compared with matched participants not living with HIV and in PLWH virally suppressed on 1 of 3 cART regimens. Methods. PLWH with a CD4+ count <300 cells/mm3 underwent standardized neurological examination and functional status assessments before and every 24 weeks after starting cART. Matched individuals not living with HIV underwent the same examinations once. Associations between covariates with DSPN at entry were assessed using the ?2 test, and virally suppressed PLWH were assessed using generalized estimating equations. Results. Before initiating cART, 21.3% of PLWH had DSPN compared with 8.5% of people not living with HIV (n = 2400; ?2(df = 1) = 96.5; P <.00001). PLWH with DSPN were more likely to report inability to work [?2(df = 1) = 10.6; P =.001] and depression [?2(df = 1) = 8.9; P =.003] than PLWH without DSPN. Overall prevalence of DSPN among those virally suppressed on cART decreased: 20.3%, week 48; 15.3%, week 144; and 10.3%, week 192. Incident DSPN was seen in 127 PLWH. Longitudinally, DSPN was more likely in older individuals (P <.001) and PLWH with less education (P =.03). There was no significant association between cART regimen and DSPN. Conclusions. Although the prevalence of DSPN decreased following cART initiation in PLWH, further research could identify strategies to prevent or ameliorate residual DSPN after initiating cART in RLSs.
AB - Background. Distal sensory peripheral neuropathy (DSPN) is a complication of human immunodeficiency virus (HIV). We estimate DSPN prevalence in 7 resource-limited settings (RLSs) for combination antiretroviral therapy (cART)-naive people living with HIV (PLWH) compared with matched participants not living with HIV and in PLWH virally suppressed on 1 of 3 cART regimens. Methods. PLWH with a CD4+ count <300 cells/mm3 underwent standardized neurological examination and functional status assessments before and every 24 weeks after starting cART. Matched individuals not living with HIV underwent the same examinations once. Associations between covariates with DSPN at entry were assessed using the ?2 test, and virally suppressed PLWH were assessed using generalized estimating equations. Results. Before initiating cART, 21.3% of PLWH had DSPN compared with 8.5% of people not living with HIV (n = 2400; ?2(df = 1) = 96.5; P <.00001). PLWH with DSPN were more likely to report inability to work [?2(df = 1) = 10.6; P =.001] and depression [?2(df = 1) = 8.9; P =.003] than PLWH without DSPN. Overall prevalence of DSPN among those virally suppressed on cART decreased: 20.3%, week 48; 15.3%, week 144; and 10.3%, week 192. Incident DSPN was seen in 127 PLWH. Longitudinally, DSPN was more likely in older individuals (P <.001) and PLWH with less education (P =.03). There was no significant association between cART regimen and DSPN. Conclusions. Although the prevalence of DSPN decreased following cART initiation in PLWH, further research could identify strategies to prevent or ameliorate residual DSPN after initiating cART in RLSs.
KW - Antiretroviral therapy
KW - HIV
KW - Peripheral neuropathy
KW - Resource-limited
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U2 - 10.1093/cid/ciz745
DO - 10.1093/cid/ciz745
M3 - Article
C2 - 31630166
AN - SCOPUS:85084074499
SN - 1058-4838
VL - 71
SP - 158
EP - 165
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 1
ER -