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Published on: September 1, 2015
CD4+ T-lymphocytes natural decrease in HAART-naïve HIV-infected adults in Abidjan
J Duvignac1, X Anglaret, A Kpozehouen
1INSERM U593, Bordeaux, France. Julien.Duvignac@isped.u-bordeaux2.fr
Insights
The natural decline of CD4 cells in HIV-infected adults in sub-Saharan Africa is similar to that in industrialized nations. Lower baseline body mass index (BMI) is linked to a faster CD4 count decrease.
Area of Science:
- Immunology
- Public Health
- Epidemiology
Background:
- Human Immunodeficiency Virus (HIV) infection leads to a decline in CD4+ T-lymphocyte counts, crucial for immune function.
- Understanding the natural history of CD4+ T-cell decline in untreated HIV-infected individuals is vital for disease management and treatment strategies.
Purpose of the Study:
- To investigate the rate of natural CD4+ T-cell decline in HIV-infected adults in sub-Saharan Africa.
- To identify factors influencing this decline, particularly in the absence of severe morbidity or highly active antiretroviral therapy (HAART).
Main Methods:
- A 7-year prospective cohort study involving biannual CD4+ T-cell measurements.
- Joint modeling approach combining a linear mixed model for CD4+ T-cell changes and a survival model for drop-out.
- Follow-up was censored at severe morbidity events or initiation of HAART.
Main Results:
- The rate of CD4+ T-cell decline was primarily associated with follow-up duration and baseline body mass index (BMI).
- Mean annual CD4+ T-cell decrease varied significantly with baseline BMI: -81/mm³ (-2.2%) for BMI 16 kg/m², -69/mm³ (-1.7%) for BMI 20.4 kg/m², and -55/mm³ (-1.2%) for BMI 25 kg/m².
- A steeper CD4+ T-cell decline was independently linked to shorter event-free follow-up periods.
Conclusions:
- The natural CD4+ T-cell decrease in sub-Saharan African adults, before HAART initiation and without severe morbidity, is comparable to rates observed in industrialized countries.
- Close monitoring of CD4+ T-cell counts is recommended for adults with low BMI in sub-Saharan African settings, where measurements may be less frequent.
Objective:
To study the CD4 natural decrease and its determinants in sub-Saharan African HIV-infected adults.
Method:
We performed a 7-year prospective cohort study, with biannual CD4 measurement. Follow-up was censored at the first severe morbidity event or at HAART initiation. Changes in CD4 values were studied by jointly modelling (a) the correlation between repeated measures through a linear mixed model and (b) the time to drop-out through a survival model.
Results:
690 patients were followed up during 1,382 person-years. Contrasting with the baseline CD4 count and percentage, which were associated with numerous variables, the slopes of both CD4 count and CD4 percentage in the absence of severe morbidity episode were only associated with the follow-up time and with the baseline body mass index (BMI). The mean annual natural decrease in CD4 count (CD4%) was estimated at -81/mm3 (-2.2%), -69/mm3 (-1.7%), and -55/mm3 (-1.2%) for patients with baseline BMI at 16 kg/m2, 20.4 kg/m2, and 25 kg/m2, respectively (p < .001). A steeper decline in the CD4 count was independently associated with a shorter event-free follow-up time.
Conclusion:
These estimates of the CD4 natural decrease in sub-Saharan African patients, while they did not experience any episode of severe morbidity and before they initiate HAART, are in the bracket of those previously reported in industrialized countries. In sub-Saharan African settings with CD4 count being measured less frequently than in industrialized countries, the CD4 should be monitored more closely among adults with low BMI.
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