Open AccessCD4 cell count and the risk of infective and non‐infective serious non‐AIDS events in HIV‐positive persons seen for care in Italy
Author(s) -
Madeddu Giordano,
D'Arminio Monforte Antonella,
Girardi Enrico,
Di Biagio Antonio,
Lo Caputo Sergio,
Piolini Roberta,
Marchetti Giulia,
Pellizzer Giampietro,
Giacometti Andrea,
Galli Laura,
Antinori Andrea,
Cozzi Lepri Alessandro
Publication year - 2014
Publication title -
journal of the international aids society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.724
H-Index - 62
ISSN - 1758-2652
DOI - 10.7448/ias.17.4.19509
Subject(s) - medicine , infective endocarditis , pneumonia , poisson regression , cohort , incidence (geometry) , pediatrics , population , physics , environmental health , optics
Serious non‐AIDS events (SNAE) are frequent in HIV patients receiving cART. Current CD4 count was shown to be more strongly associated with infective compared to not‐infective SNAE and unable to predict cardiovascular events. We investigated the relationship between baseline and current CD4 count and the risk of both infective and non‐infective SNAE in HIV‐positive patients according to current ART use. Methods We included all HIV‐positive persons enrolled in the ICONA Foundation Study cohort who had at least one follow‐up visit. SNAE were grouped in infective (pneumonia, sepsis, endocarditis and meningitis) and non‐infective (malignancies, chronic kidney disease, cardiovascular events, hepatic events and pancreatitis) aetiology. Incidence of these event groups were calculated overall and according to baseline and current CD4 count (grouped as 0–200, 201–350, 351–500, 501–750, and >750 cells/mm 3 ). Participants’ follow‐up accrued from the date of enrolment (baseline) to a diagnosis of SNAE or their last visit. An event was defined the first time one of the considered SNAE occurred so that each person contributed a single event. A Poisson regression model for each of the two endpoints was used. Results A total of 10,822 patients were included (25.3% females, 38.2% heterosexuals) and 26.6% had hepatitis co‐infections. Median age was 36 (IQR 31–42) years. Overall, 423 not‐infective and 385 infective SNAE were included. The most frequent non‐infective SNAE were malignancies ( n =202) and the most frequent infective SNAE were pneumonia ( n =289). Crude rates of non‐infective SNAE were 0.78, 1.08 and 0.80/100 PYFU, and those of infective SNAE were 1.00, 0.51 and 0.66/100 PYFU in ART naive, currently off and currently on ART patients, respectively. Higher current CD4 count was associated with reduced risk of both infective and non‐infective SNAE in naives and in patients on ART (Table 1). The association was less strong in the group which suspended ART (for non‐infective SNAE the p value for interaction between current log‐CD4 and ART‐status, p =0.004). Conversely, we found no association between baseline CD4 count and risk of non‐infective SNAE in people treated with ART ( p value for interaction = 0.0001). When CVD were considered separately, there was no association with CD4 count (not shown). Conclusions Our findings show that, differently from ART naive, in ART‐treated patients, non‐infective SNAE are predicted by current but not by baseline CD4, suggesting that immune restoration is crucial to prevent these events.