TY - JOUR
T1 - The use of plasma androstenedione in monitoringtherapy of patients with congenital adrenal hyperplasia
AU - Cavallo, Anita
AU - Corn, Carolyn
AU - Bryan, George T.
AU - Meyer, Walter J.
N1 - Funding Information:
From the Department of Pediatrics, University of Texas Medical Branch " Some patients were studied on the Clinical Research Center of the University of Texas Medical Branch Supported by Grant RR-73 from the General Clinical Research Centers Program of Division of Research Resources, National Institutes of Health," the research was supported by the Department of Pediatrics, University of Texas Medical Branch, Galveston. *Reprint address: Division of Endocrinology, Depm'tment of Pediatrics, University of Texas Medical Branch, Galveston, TX 77550.
PY - 1979/7
Y1 - 1979/7
N2 - Therapy of congenital adrenal hyperplasia transidtionally is monitored by the amount of urinary 17-KS. However, 24-hour urine collections are difficult to obtain and are often unreliable. Measurement of the plasma concentrations of androgens, such as Δ or T, would therefore be a more convenient way to determine the efficacy of treatment. Over a period of 2 to 24 months, 23 patients were periodically assessed by clinical examination, bone age, and determinations of plasma Δ, plasma T, and 24-hour urinary 17-KS. Plasma T concentration correlated well with clinical control in females and in preadolescent males, but not in infant and pubertal males. By contrast, plasma Δ concentration correlated well with clinical control in either sex, regardless of stage of puberty. The present study suggests that monitoring plasma Δ concentration is useful in the long-term management of patients with CAH.
AB - Therapy of congenital adrenal hyperplasia transidtionally is monitored by the amount of urinary 17-KS. However, 24-hour urine collections are difficult to obtain and are often unreliable. Measurement of the plasma concentrations of androgens, such as Δ or T, would therefore be a more convenient way to determine the efficacy of treatment. Over a period of 2 to 24 months, 23 patients were periodically assessed by clinical examination, bone age, and determinations of plasma Δ, plasma T, and 24-hour urinary 17-KS. Plasma T concentration correlated well with clinical control in females and in preadolescent males, but not in infant and pubertal males. By contrast, plasma Δ concentration correlated well with clinical control in either sex, regardless of stage of puberty. The present study suggests that monitoring plasma Δ concentration is useful in the long-term management of patients with CAH.
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U2 - 10.1016/S0022-3476(79)80078-5
DO - 10.1016/S0022-3476(79)80078-5
M3 - Article
C2 - 480011
AN - SCOPUS:0018398563
SN - 0022-3476
VL - 95
SP - 33
EP - 37
JO - The Journal of Pediatrics
JF - The Journal of Pediatrics
IS - 1
ER -