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      Pituitary-adrenal axis function in sickle cell anemia and its relationship to leukocyte alkaline phosphatase.

      American Journal of Hematology
      Adult, Alkaline Phosphatase, blood, Anemia, Sickle Cell, physiopathology, Blood Glucose, metabolism, Cortodoxone, Female, Growth Hormone, Humans, Hydrocortisone, Insulin, pharmacology, Leukocytes, enzymology, Male, Metyrapone, Pituitary-Adrenal System, Thalassemia

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          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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