Neurocognitive performance enhanced by highly active antiretroviral therapy in HIV-infected women

被引:84
作者
Cohen, RA [1 ]
Boland, R
Paul, R
Tashima, KT
Schoenbaum, EE
Celentano, DD
Schuman, P
Smith, DK
Carpenter, CCJ
机构
[1] Brown Univ, Sch Med, Providence, RI 02912 USA
[2] Montefiore Med Ctr, New York, NY USA
[3] Albert Einstein Coll Med, New York, NY USA
[4] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[5] Wayne State Univ, Sch Med, Detroit, MI USA
[6] Ctr Dis Control & Prevent, Atlanta, GA USA
关键词
HAART; highly active antiretroviral treatment; neurocognitive status; CD4 cell count; neurocognitive tests;
D O I
10.1097/00002030-200102160-00007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To determine whether highly active retroviral therapy (HAART) is associated with better neurocognitive outcome overtime among HIV-infected women with severely impaired immune function. Methods: A semiannual neurocognitive examination on four tasks was administered: Color Trail Making, Controlled Oral Word Association, Grooved Pegboard and Four-Word Learning. This protocol was initiated in the HIV Epidemiological Research study (HERS) study when a woman's CD4 cell count fell to < 100 x 10(6) cells/l. Immune function (CD4), viral load status and depression severity (CESD) were also assessed semi-annually, along with an interview to determine medication intake and illicit drug use. Results: HAART was not available to any participant at the rime of enrollment (baseline), while 44% reported taking HAART at their most recent visit (mean duration of HAART 36.3 +/- 12.6 months). HAART-treated women had improved neurocognitive performance compared with those not treated with HAART. Women taking HAART for 18 months or more showed the strongest neurocognitive performance with improved verbal fluency psychomotor and executive functions. These functions worsened among women not taking HAART. Substance abuse status, severity of depressive symptoms, age and educational revel did not influence the HAART treatment effects on neurocognitive performance. Neurocognitive improvements were strongly associated with the magnitude of CD4 cell count increases. Conclusions: HAART appeared to produce beneficial effect on neurocognitive functioning in HIV-infected women with severely impaired immune systems. Benefits were greatest for women who reported receiving HAART for more than 18 months. (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:341 / 345
页数:5
相关论文
共 24 条
[1]  
[Anonymous], 1963, MED CLIN N AM
[2]   Levels of human immunodeficiency virus type 1 RNA in cerebrospinal fluid correlate with AIDS dementia stage [J].
Brew, BJ ;
Pemberton, L ;
Cunningham, P ;
Law, MG .
JOURNAL OF INFECTIOUS DISEASES, 1997, 175 (04) :963-966
[3]   Effect of combination therapy with zidovudine and didanosine on neuropsychological functioning in patients with symptomatic HIV disease: A comparison of simultaneous and alternating regimens [J].
Brouwers, P ;
Hendricks, M ;
Lietzau, JA ;
Pluda, JM ;
Mitsuya, H ;
Broder, S ;
Yarchoan, R .
AIDS, 1997, 11 (01) :59-66
[4]   QUIESCENT LYMPHOCYTES-T AS AN INDUCIBLE VIRUS RESERVOIR IN HIV-1 INFECTION [J].
BUKRINSKY, MI ;
STANWICK, TL ;
DEMPSEY, MP ;
STEVENSON, M .
SCIENCE, 1991, 254 (5030) :423-427
[5]  
*CDC, 1999, HIV AIDS SURVEILLANC, V11, P1
[6]  
Cohen R. A., 1993, NEUROPSYCHOLOGY ATTE
[7]  
DELIA L, 1996, PSYCHOL ASSESSMENT
[8]   Cerebrospinal fluid HIV-1 RNA during treatment with ritonavir/saquinavir or ritonavir/saquinavir/stavudine [J].
Gisolf, EH ;
Enting, RH ;
Jurriaans, S ;
de Wolf, F ;
van der Ende, ME ;
Hoetelmans, RMW ;
Portegies, P ;
Danner, SA .
AIDS, 2000, 14 (11) :1583-1589
[9]   A trial comparing nucleoside monotherapy with combination therapy in HIV-infected adults with CD4 cell counts from 200 to 500 per cubic millimeter [J].
Hammer, SM ;
Katzenstein, DA ;
Hughes, MD ;
Gundacker, H ;
Schooley, RT ;
Haubrich, RH ;
Henry, WK ;
Lederman, MM ;
Phair, JP ;
Niu, M ;
Hirsch, MS ;
Merigan, TC ;
Blaschke, TF ;
Simpson, D ;
McLaren, C ;
Rooney, J ;
Salgo, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (15) :1081-1090
[10]  
Heaton R K, 1995, J Int Neuropsychol Soc, V1, P231