M. Arnadottir et al., ADRENOCORTICOTROPIC HORMONE LOWERS SERUM LP(A) AND LDL CHOLESTEROL CONCENTRATIONS IN HEMODIALYSIS-PATIENTS, Kidney international, 52(6), 1997, pp. 1651-1655
Previously, we have shown that short-term administration of adrenocort
icotrophic hormone (ACTH) results in reduced concentrations of apolipo
protein B-containing lipoproteins, including lipoprotein(a), and reduc
ed activities of hepatic lipase. These effects were observed in steroi
d-treated patients suffering from iatrogenic ACTH deficiency and in he
althy individuals. The direct nature of the influence of ACTH on hepat
ic lipoprotein metabolism was confirmed by in vitro experiments. The a
im of the present investigation was to study the effects of ACTH treat
ment on uremic patients, who exhibit disturbed lipoprotein pattern due
to the slow removal of triglyceride-rich lipoproteins and who probabl
y are ACTH resistant. Eight patients on chronic hemodialysis were stud
ied. After one intramuscular injection of Synacthen Depot (a synthetic
ACTH(1-24) preparation from Ciba Geigy AG, Basel, Switzerland) 1 mg,
the only change noted was a significant reduction of 26% in median lip
oprotein(a) concentration. After five injections, a further decrease (
65%) was found in the lipoprotein(a) concentration. Also, reductions i
n median concentrations of total cholesterol, low density lipoprotein
cholesterol and apolipoprotein B were observed. The magnitude of these
changes was 15 to 30%. In contrast to previously studied groups, no c
hanges were observed regarding triglyceride metabolism. Significantly
increased median concentration of apolipoprotein CIII was found. Howev
er, the excess apolipoprotein CIII was confined to the fraction that w
as not associated with apolipoprotein B. Thus, administration of ACTH
to uremic patients improved their atherogenic lipoprotein profile, a f
act that may have future therapeutic implications. In comparison to pr
eviously studied groups, the uremic patients responded rather slowly a
nd not at all regarding triglyceride metabolism.