C. Allavena et al., RELATIONSHIP OF TRACE-ELEMENT, IMMUNOLOGICAL MARKERS, AND HIV-1 INFECTION PROGRESSION, Biological trace element research, 47(1-3), 1995, pp. 133-138
Trace elements (selenium, zinc, copper), beta(2) microglobulin levels,
CD4, and CD8 cell counts have been determined in 80 HIV1 seropositive
patients. The study group consisted of 19 females and 61 males with a
ge mean of 35 +/- 10 yr, at stage IV of infection (CDC-Atlanta classif
ication) and treated by AZT. No severe renal or liver diseases or hypo
albuminemia were observed in this group.Se values were significantly l
ower than in normal adults, 48.3 +/- 17 mu g/L vs 71 +/- 12 mu g/L; Zn
was moderately diminished, 1 +/- 0.2 mg/L vs 1.2 +/- 0.2 mg/L, wherea
s copper values were in the normal range, 1.2 +/- 0.3 mg/L vs 1.1 +/-
0.5 mg/L. Se or Zn deficiency was found in 60 and 30 subjects, respect
ively. Blood Se and Zn decreases were associated in 23 patients. Moreo
ver, all patients showed higher beta(2) microglobulin values than the
upper normal limit of 2.4 mg/L. Negative correlations were found betwe
en Zn and beta 2 microglobulin (p < 0.005) and between Se and beta(2)
microglobulin (p < 0.05). Moreover, there was a positive correlation b
etween Se and Zn values (p < 0.05). Nineteen subjects died 1 yr later
(group I), and 61 remained alive (group II). With respect to the clini
cal evolution, a significant difference between both groups was found
in Se and beta 2 microglobulin levels as well as in CD4 cell counts. T
he correlations previously observed persisted in group II, whereas no
correlation was noted in group I. In addition, the patients of group I
had significantly lower Se values, which were below 30 mu g/L in 10 c
ases. These results confirm the prevalence of abnormalities in Se and
Zn levels and their relationships with nonspecific markers of immune s
ystem activity in more advanced HIV disease. Impairment of trace eleme
nt status and mainly Se status appeared, at least partially, to reflec
t the disease activity/progression and subsequently the immune dysregu
lation.