Mortality of treated HIV-1 positive individuals according to viral subtype in Europe and Canada: collaborative cohort analysis
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Author(s)
Type
Journal Article
Abstract
Objectives: To estimate prognosis by viral subtype in HIV-1-infected individuals from
start of antiretroviral therapy (ART) and after viral failure.
Design: Collaborative analysis of data from eight European and three Canadian
cohorts.
Methods: Adults (N>20 000) who started triple ART between 1996 and 2012 and
had data on viral subtype were followed for mortality. We estimated crude and
adjusted (for age, sex, regimen, CD4þ cell count, and AIDS at baseline, period of
starting ART, stratified by cohort, region of origin and risk group) mortality hazard
ratios (MHR) by subtype. We estimated MHR subsequent to viral failure defined as
two HIV-RNA measurements greater than 500 copies/ml after achieving viral
suppression.
Results: The most prevalent subtypes were B (15 419; 74%), C (2091; 10%), CRF02AG
(1057; 5%), A (873; 4%), CRF01AE (506; 2.4%), G (359; 1.7%), and D (232; 1.1%).
Subtypes were strongly patterned by region of origin and risk group. During 104 649
person-years of observation, 1172/20 784 patients died. Compared with subtype B,
mortality was higher for subtype A, but similar for all other subtypes. MHR for A versus B
were 1.13 (95% confidence interval 0.85,1.50) when stratified by cohort, increased to
1.78 (1.27,2.51) on stratification by region and risk, and attenuated to 1.59 (1.14,2.23)
on adjustment for covariates. MHR for A versus B was 2.65 (1.64,4.28) and 0.95
(0.57,1.57) for patients who started ART with CD4þ cell count below, or more than, 100
cells/ml, respectively. There was no difference in mortality between subtypes A, B and C
after viral failure.
Conclusion: Patients with subtype A had worse prognosis, an observation which may
be confounded by socio-demographic factors.
start of antiretroviral therapy (ART) and after viral failure.
Design: Collaborative analysis of data from eight European and three Canadian
cohorts.
Methods: Adults (N>20 000) who started triple ART between 1996 and 2012 and
had data on viral subtype were followed for mortality. We estimated crude and
adjusted (for age, sex, regimen, CD4þ cell count, and AIDS at baseline, period of
starting ART, stratified by cohort, region of origin and risk group) mortality hazard
ratios (MHR) by subtype. We estimated MHR subsequent to viral failure defined as
two HIV-RNA measurements greater than 500 copies/ml after achieving viral
suppression.
Results: The most prevalent subtypes were B (15 419; 74%), C (2091; 10%), CRF02AG
(1057; 5%), A (873; 4%), CRF01AE (506; 2.4%), G (359; 1.7%), and D (232; 1.1%).
Subtypes were strongly patterned by region of origin and risk group. During 104 649
person-years of observation, 1172/20 784 patients died. Compared with subtype B,
mortality was higher for subtype A, but similar for all other subtypes. MHR for A versus B
were 1.13 (95% confidence interval 0.85,1.50) when stratified by cohort, increased to
1.78 (1.27,2.51) on stratification by region and risk, and attenuated to 1.59 (1.14,2.23)
on adjustment for covariates. MHR for A versus B was 2.65 (1.64,4.28) and 0.95
(0.57,1.57) for patients who started ART with CD4þ cell count below, or more than, 100
cells/ml, respectively. There was no difference in mortality between subtypes A, B and C
after viral failure.
Conclusion: Patients with subtype A had worse prognosis, an observation which may
be confounded by socio-demographic factors.
Date Issued
2016-01-28
Date Acceptance
2015-10-07
Citation
AIDS, 2016, 30 (3), pp.503-513
ISSN
0269-9370
Publisher
Lippincott, Williams & Wilkins
Start Page
503
End Page
513
Journal / Book Title
AIDS
Volume
30
Issue
3
License URL
Subjects
Science & Technology
Life Sciences & Biomedicine
Immunology
Infectious Diseases
Virology
antiretroviral therapy
HIV-1 subtype
mortality
prognosis
viral failure
COMBINATION ANTIRETROVIRAL THERAPY
T-CELL DECLINE
DISEASE PROGRESSION
IMMUNOLOGICAL RESPONSE
TYPE-1 SUBTYPES
NAIVE PATIENTS
IMPACT
DIVERSITY
INFECTIONS
RESISTANCE
Publication Status
Published