21-hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder

A multicenter study

Carlos Moran, Ricardo Azziz, Enrico Carmina, Didier Dewailly, Franca Fruzzetti, Lourdes Ibañez, Eric S. Knochenhauer, Jose A.M. Marcondes, Berenice B. Mendonca, Duarte Pignatelli, Michel Pugeat, Vincent Rohmer, Phyllis W. Speiser, Selma F. Witchel

Research output: Contribution to journalArticle

119 Citations (Scopus)

Abstract

OBJECTIVE: Our aim was to determine whether the clinical features of 21-hydroxylase-deficient nonclassic adrenal hyperplasia are correlated with either age at symptom onset or age at presentation, or both, and with the degree of adrenocortical abnormality. STUDY DESIGN: In a multicenter cohort design 220 women with nonclassic adrenal hyperplasia, with a basal or adrenocorticotropic hormone - stimulated 17-hydroxyprogesterone level >30.3 nmol/L, were studied, either prospectively (n = 39) or retrospectively (n = 181). Patients were stratified by age of presentation into 5 groups: (1) <10 years (n = 25), (2) 10 to 19 years (n = 64), (3) 20 to 29 years (n = 83), (4) 30 to 39 years (n = 30), and (5) 40 to 49 years (n = 16). Two patients >50 years old were excluded from the analysis because of age. RESULTS: Ninety-two percent of patients <10 years old had premature pubarche at presentation, whereas clitoromegaly and acne were each present in only 20% of these younger subjects. With only patients ≥10 years old considered, presenting clinical features included hirsutism (59%), oligomenorrhea (54%), acne (33%), infertility (13%), clitoromegaly (10%), alopecia (8%), primary amenorrhea (4%), and premature pubarche (4%). Among the patients ≥10 years old, the prevalence but not the degree of hirsutism increased significantly with age. Basal levels of 17-hydroxyprogesterone in adolescents were significantly higher than the levels found either in children (<10 years old) or women 40 to 49 years old (P < .01 and P < .03, respectively), although no difference was noted in the stimulated 17-hydroxyprogesterone levels between age groups. The adrenocorticotropic hormone-stimulated levels but not the basal levels of 17-hydroxyprogesterone were significantly higher in patients with clitoromegaly than in women without clitoromegaly. Alternatively, there were no differences in either basal or stimulated 17-hydroxyprogesterone levels between patients with and those without hirsutism, acne, or alopecia. CONCLUSION: In children <10 years old the most common presenting complaint was premature pubarche, whereas hirsutism and oligomenorrhea were more common in older patients. The prevalence of hirsutism increased with age, suggesting the progressive nature of nonclassic adrenal hyperplasia. Furthermore, the adrenocorticotropic hormone-stimulated levels of 17-hydroxyprogesterone were higher in patients with clitoromegaly, which suggests that the degree of adrenocortical dysfunction in nonclassic adrenal hyperplasia determines, at least in part, the clinical presentation.

Original languageEnglish (US)
Pages (from-to)1468-1474
Number of pages7
JournalAmerican Journal of Obstetrics and Gynecology
Volume183
Issue number6
DOIs
StatePublished - Jan 1 2000

Fingerprint

Steroid 21-Hydroxylase
17-alpha-Hydroxyprogesterone
Multicenter Studies
Hyperplasia
Hirsutism
Acne Vulgaris
Oligomenorrhea
Adrenocorticotropic Hormone
Alopecia
Amenorrhea
Age of Onset
Infertility
Age Groups

Keywords

  • 21-hydroxylase
  • Acne
  • Adrenal hyperplasia
  • Clitoromegaly
  • Hirsutism

ASJC Scopus subject areas

  • Obstetrics and Gynecology

Cite this

Moran, C., Azziz, R., Carmina, E., Dewailly, D., Fruzzetti, F., Ibañez, L., ... Witchel, S. F. (2000). 21-hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study. American Journal of Obstetrics and Gynecology, 183(6), 1468-1474. https://doi.org/10.1067/mob.2000.108020

21-hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder : A multicenter study. / Moran, Carlos; Azziz, Ricardo; Carmina, Enrico; Dewailly, Didier; Fruzzetti, Franca; Ibañez, Lourdes; Knochenhauer, Eric S.; Marcondes, Jose A.M.; Mendonca, Berenice B.; Pignatelli, Duarte; Pugeat, Michel; Rohmer, Vincent; Speiser, Phyllis W.; Witchel, Selma F.

In: American Journal of Obstetrics and Gynecology, Vol. 183, No. 6, 01.01.2000, p. 1468-1474.

Research output: Contribution to journalArticle

Moran, C, Azziz, R, Carmina, E, Dewailly, D, Fruzzetti, F, Ibañez, L, Knochenhauer, ES, Marcondes, JAM, Mendonca, BB, Pignatelli, D, Pugeat, M, Rohmer, V, Speiser, PW & Witchel, SF 2000, '21-hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study', American Journal of Obstetrics and Gynecology, vol. 183, no. 6, pp. 1468-1474. https://doi.org/10.1067/mob.2000.108020
Moran, Carlos ; Azziz, Ricardo ; Carmina, Enrico ; Dewailly, Didier ; Fruzzetti, Franca ; Ibañez, Lourdes ; Knochenhauer, Eric S. ; Marcondes, Jose A.M. ; Mendonca, Berenice B. ; Pignatelli, Duarte ; Pugeat, Michel ; Rohmer, Vincent ; Speiser, Phyllis W. ; Witchel, Selma F. / 21-hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder : A multicenter study. In: American Journal of Obstetrics and Gynecology. 2000 ; Vol. 183, No. 6. pp. 1468-1474.
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T1 - 21-hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder

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AU - Moran, Carlos

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AU - Carmina, Enrico

AU - Dewailly, Didier

AU - Fruzzetti, Franca

AU - Ibañez, Lourdes

AU - Knochenhauer, Eric S.

AU - Marcondes, Jose A.M.

AU - Mendonca, Berenice B.

AU - Pignatelli, Duarte

AU - Pugeat, Michel

AU - Rohmer, Vincent

AU - Speiser, Phyllis W.

AU - Witchel, Selma F.

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AB - OBJECTIVE: Our aim was to determine whether the clinical features of 21-hydroxylase-deficient nonclassic adrenal hyperplasia are correlated with either age at symptom onset or age at presentation, or both, and with the degree of adrenocortical abnormality. STUDY DESIGN: In a multicenter cohort design 220 women with nonclassic adrenal hyperplasia, with a basal or adrenocorticotropic hormone - stimulated 17-hydroxyprogesterone level >30.3 nmol/L, were studied, either prospectively (n = 39) or retrospectively (n = 181). Patients were stratified by age of presentation into 5 groups: (1) <10 years (n = 25), (2) 10 to 19 years (n = 64), (3) 20 to 29 years (n = 83), (4) 30 to 39 years (n = 30), and (5) 40 to 49 years (n = 16). Two patients >50 years old were excluded from the analysis because of age. RESULTS: Ninety-two percent of patients <10 years old had premature pubarche at presentation, whereas clitoromegaly and acne were each present in only 20% of these younger subjects. With only patients ≥10 years old considered, presenting clinical features included hirsutism (59%), oligomenorrhea (54%), acne (33%), infertility (13%), clitoromegaly (10%), alopecia (8%), primary amenorrhea (4%), and premature pubarche (4%). Among the patients ≥10 years old, the prevalence but not the degree of hirsutism increased significantly with age. Basal levels of 17-hydroxyprogesterone in adolescents were significantly higher than the levels found either in children (<10 years old) or women 40 to 49 years old (P < .01 and P < .03, respectively), although no difference was noted in the stimulated 17-hydroxyprogesterone levels between age groups. The adrenocorticotropic hormone-stimulated levels but not the basal levels of 17-hydroxyprogesterone were significantly higher in patients with clitoromegaly than in women without clitoromegaly. Alternatively, there were no differences in either basal or stimulated 17-hydroxyprogesterone levels between patients with and those without hirsutism, acne, or alopecia. CONCLUSION: In children <10 years old the most common presenting complaint was premature pubarche, whereas hirsutism and oligomenorrhea were more common in older patients. The prevalence of hirsutism increased with age, suggesting the progressive nature of nonclassic adrenal hyperplasia. Furthermore, the adrenocorticotropic hormone-stimulated levels of 17-hydroxyprogesterone were higher in patients with clitoromegaly, which suggests that the degree of adrenocortical dysfunction in nonclassic adrenal hyperplasia determines, at least in part, the clinical presentation.

KW - 21-hydroxylase

KW - Acne

KW - Adrenal hyperplasia

KW - Clitoromegaly

KW - Hirsutism

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