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Treatment of acromegaly with the growth hormone-receptor antagonist pegvisomant.

Trainer, P J (author)
Drake, W M (author)
Katznelson, L (author)
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Freda, P U (author)
Herman-Bonert, V (author)
van der Lely, A J (author)
Dimaraki, E V (author)
Stewart, P M (author)
Friend, K E (author)
Vance, M L (author)
Besser, G M (author)
Scarlett, J A (author)
Thorner, M O (author)
Parkinson, C (author)
Klibanski, A (author)
Powell, J S (author)
Barkan, A L (author)
Sheppard, M C (author)
Malsonado, M (author)
Rose, D R (author)
Clemmons, D R (author)
Johannsson, Gudmundur, 1960 (author)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för kroppssammansättning och metabolism,Institute of Internal Medicine, Dept of Body Composition and Metabolism
Bengtsson, B A (author)
Stavrou, S (author)
Kleinberg, D L (author)
Cook, D M (author)
Phillips, L S (author)
Bidlingmaier, M (author)
Strasburger, C J (author)
Hackett, S (author)
Zib, K (author)
Bennett, W F (author)
Davis, R J (author)
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 (creator_code:org_t)
2000
2000
English.
In: The New England journal of medicine. - 0028-4793. ; 342:16, s. 1171-7
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Patients with acromegaly are currently treated with surgery, radiation therapy, and drugs to reduce hypersecretion of growth hormone, but the treatments may be ineffective and have adverse effects. Pegvisomant is a genetically engineered growth hormone-receptor antagonist that blocks the action of growth hormone.We conducted a 12-week, randomized, double-blind study of three daily doses of pegvisomant (10 mg, 15 mg, and 20 mg) and placebo, given subcutaneously, in 112 patients with acromegaly.The mean (+/-SD) serum concentration of insulin-like growth factor I (IGF-I) decreased from base line by 4.0+/-16.8 percent in the placebo group, 26.7+/-27.9 percent in the group that received 10 mg of pegvisomant per day, 50.1+/-26.7 percent in the group that received 15 mg of pegvisomant per day, and 62.5+/-21.3 percent in the group that received 20 mg of pegvisomant per day (P<0.001 for the comparison of each pegvisomant group with placebo), and the concentrations became normal in 10 percent, 54 percent, 81 percent, and 89 percent of patients, respectively (P<0.001 for each comparison with placebo). Among patients treated with 15 mg or 20 mg of pegvisomant per day, there were significant decreases in ring size, soft-tissue swelling, the degree of excessive perspiration, and fatigue. The score fortotal symptoms and signs of acromegaly decreased significantly in all groups receiving pegvisomant (P< or =0.05). The incidence of adverse effects was similar in all groups.On the basis of these preliminary results, treatment of patients who have acromegaly with a growth hormone-receptor antagonist results in a reduction in serum IGF-I concentrations and in clinical improvement.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Keyword

Acromegaly
blood
drug therapy
Adenoma
drug therapy
pathology
Adult
Autoantibodies
blood
Double-Blind Method
Female
Human Growth Hormone
adverse effects
analogs & derivatives
blood
immunology
therapeutic use
Humans
Insulin-Like Growth Factor I
metabolism
Male
Middle Aged
Pituitary Neoplasms
drug therapy
pathology
Receptors
Somatotropin
antagonists & inhibitors

Publication and Content Type

ref (subject category)
art (subject category)

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