Volume 9, Issue 4 pp. 373-379
Original Article
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Pituitary-adrenal axis function in sickle cell anemia and its relationship to leukocyte alkaline phosphatase

Barry E. Rosenbloom

Barry E. Rosenbloom

Department of Medicine, Harbor-UCLA Medical Center, Torrance, California

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William D. Odell

William D. Odell

Department of Medicine, Harbor-UCLA Medical Center, Torrance, California

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Kouichi R. Tanaka

Corresponding Author

Kouichi R. Tanaka

Department of Medicine, Harbor-UCLA Medical Center, Torrance, California

Department of Medicine, Harbor-UCLA Medical Center, 1000 West Carson Street, Torrance, CA 90509Search for more papers by this author
First published: December 1980
Citations: 6

Abstract

The function of the pituitary-adrenal axis and leukocyte alkaline phosphatase activity were evaluated in eight patients with sickle cell disease during a painful crisis and when crisis-free. The leukocyte alkaline phosphatase (LAP) score did not increase during crisis; the scores were in the low-normal range during crisis and noncrisis periods. Insulin-induced hypoglycemia produced normal growth hormone responses during both crisis and crisis-free periods. Plasma cortisol concentrations were diminished in the crisis group. Also impaired was 11-deoxycortisol production in both groups after metyrapone. These findings indicate that a mild defect in the hypothalamic-pituitary-adrenal axis exists in sickle cell disease patients.

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