N. Schinaia et al., CLINICAL FACTORS ASSOCIATED WITH PROGRESSION TO AIDS IN THE ITALIAN COHORT OF HIV-POSITIVE HEMOPHILIACS, Thrombosis and haemostasis, 72(1), 1994, pp. 33-38
This study updates estimates of the cumulative incidence of AIDS among
Italian patients with congenital coagulation disorders (mostly hemoph
iliacs), and elucidates the role of age at seroconversion? type and am
ount of replacement therapy, and HBV co-infection in progression. Info
rmation was collected both retrospectively and prospectively on 767 HI
V-I positive patients enrolled in the on-going national registry of pa
tients with congenital coagulation disorders. The seroconversion date
was estimated as the median point of each patient's seroconversion int
erval, under a Weibull distribution applied to the overall interval. T
he independence of factors associated to faster progression was assess
ed by multivariate analysis. The cumulative incidence of AIDS was esti
mated using the Kaplan-Meier survival analysis at 17.0% (95% CI = 14.1
-19.9%) over an 8-year period for Italian hemophiliacs. Patients with
age greater than or equal to 35 pears exhibited the highest cumulative
incidence of AIDS over the same time period, 32.5% (95% CI = 22.2-42.
8%). Factor IX recipients (i.e. severe B hemophiliacs) had higher cumu
lative incidence of AIDS (23.3% vs 14.2%, p = 0.01) than factor VIII r
ecipients (i.e. severe A hemophiliacs)l as aid severe A hemophiliacs o
n less-than-20,000 IU/yearly of plasma-derived clotting factor concent
rates, as opposed to A hemophiliacs using an average of more than 20,0
00 IU (18.8% vs 10.9%, p = 0.02). No statistically significant differe
nce in progression was observed between HBsAg-positive vs HBsAg-negati
ve hemophiliacs (10.5% vs 16.4%, p = 0.10). Virological, immunological
or both reasons can account for such findings, and should be investig
ated from the laboratory standpoint.