No Difference in Clinical Progression between Patients Infected with the Predominant Human Immunodeficiency Virus Type 1 Circulating Recombinant Form (CRF) 02_AG Strain and Patients Not Infected with CRF02_AG, in Western and West‐Central Africa: A Four‐Year Prospective Multicenter Study
Author(s) -
Christian Laurent,
Anke Bourgeois,
Mame Awa Faye,
Rose Mougnutou,
Moussa Seydi,
Mandoumbe Guèye,
Florian Liégeois,
Coumba Touré Kane,
Christelle Butel,
Josephine Mbuagbaw,
Léopold Zekeng,
Souleymane Mboup,
Eitel MpoudiNgolé,
Martine Peeters,
Éric Delaporte
Publication year - 2002
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/341833
Subject(s) - viral disease , virology , virus , confidence interval , sida , recombinant dna , prospective cohort study , strain (injury) , immunopathology , medicine , immunology , biology , gastroenterology , gene , biochemistry
To compare human immunodeficiency virus (HIV) type 1 disease progression in patients infected by the predominant strain circulating recombinant form (CRF) 02_AG in western and west-central Africa and in patients infected by other strains, a prospective multicenter cohort study was conducted in Cameroon and Senegal. Among the 335 patients, a broad HIV-1 group M subtype diversity was observed in the envelope V3-V5 region, but strain CRF02_AG predominated in both Cameroon and Senegal (61.2% and 62.9%, respectively; P<.8). Multivariate analyses showed no difference between patients infected by CRF02 strains and those infected by other strains in terms of survival (adjusted hazards ratio [HR], 1.16; 95% confidence interval [CI], 0.76-1.78; P=.5), clinical disease progression (HR, 0.79; 95% CI, 0.50-1.25; P=.3), or square root CD4 cell decline (regression coefficient, -0.01; 95% CI, -0.82 to 0.81; P=.9). This study suggests that the predominance of HIV-1 CRF02_AG strain in western and west-central Africa should have no major clinical consequences.
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