Obesity, acanthosis nigricans, insulin resistance, and hyperandrogenemia

Pediatric perspective and natural history

Gail E. Richards, Anita Cavallo, Walter Meyer, Melvin J. Prince, Edward J. Peters, Charles A. Stuart, Edward R. Smith

Research output: Contribution to journalArticle

72 Citations (Scopus)

Abstract

We studied the syndrome of acanthosis nigricans, obesity, insulin resistance, and hyperandrogenemia in 22 patients. Although isolated case reports in adolescents have appeared, this syndrome has not received full recognition as a pediatric entity. Our patients (17 girls, five boys) had a mean weight 5.7 SD above the mean for age, although mean height was only 0.5 SD above the mean for age. All patients had acanthosis nigricans. Their insulin resistance was significantly greater than that in a control group with comparable obesity. Fasting insulin concentration was 5.25 μU/ml in lean controls, 19.6 μU/ml in obese controls, and 49.8 μU/ml in study patients (P<0.002). Mean glucose disappearance rate during an insulin tolerance test was 6.7%/min in lean controls, 5.19%/min in obese controls, and 2.35%/min in study patients (P<0.02). After menarche, mean plasma testosterone concentration was 106 ng/dl, compared with <50 ng/dl in all lean and obese control patients. Data derived from our series of patients lead us to conclude that (1) this is a genetic syndrome, although the exact mode of inheritance is unclear; (2) the natural history of the syndrome invariably begins with the onset of obesity, followed by acanthosis nigricans that worsens with progressive weight gain; (3) acanthosis nigricans is thus a marker for hyperinsulinemia, which occurs before hyperandrogenemia; (4) hyperandrogenemia occurs only after menarche. Identification of this syndrome should permit monitoring for the development of hyperandrogenemia during puberty and determination of other affected family members.

Original languageEnglish (US)
Pages (from-to)893-897
Number of pages5
JournalThe Journal of pediatrics
Volume107
Issue number6
DOIs
StatePublished - 1985

Fingerprint

Acanthosis Nigricans
Natural History
Insulin Resistance
Obesity
Pediatrics
Menarche
Insulin
Hyperinsulinism
Puberty
Weight Gain
Testosterone
Fasting
Weights and Measures
Glucose
Control Groups

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Richards, G. E., Cavallo, A., Meyer, W., Prince, M. J., Peters, E. J., Stuart, C. A., & Smith, E. R. (1985). Obesity, acanthosis nigricans, insulin resistance, and hyperandrogenemia: Pediatric perspective and natural history. The Journal of pediatrics, 107(6), 893-897. https://doi.org/10.1016/S0022-3476(85)80182-7

Obesity, acanthosis nigricans, insulin resistance, and hyperandrogenemia : Pediatric perspective and natural history. / Richards, Gail E.; Cavallo, Anita; Meyer, Walter; Prince, Melvin J.; Peters, Edward J.; Stuart, Charles A.; Smith, Edward R.

In: The Journal of pediatrics, Vol. 107, No. 6, 1985, p. 893-897.

Research output: Contribution to journalArticle

Richards, GE, Cavallo, A, Meyer, W, Prince, MJ, Peters, EJ, Stuart, CA & Smith, ER 1985, 'Obesity, acanthosis nigricans, insulin resistance, and hyperandrogenemia: Pediatric perspective and natural history', The Journal of pediatrics, vol. 107, no. 6, pp. 893-897. https://doi.org/10.1016/S0022-3476(85)80182-7
Richards, Gail E. ; Cavallo, Anita ; Meyer, Walter ; Prince, Melvin J. ; Peters, Edward J. ; Stuart, Charles A. ; Smith, Edward R. / Obesity, acanthosis nigricans, insulin resistance, and hyperandrogenemia : Pediatric perspective and natural history. In: The Journal of pediatrics. 1985 ; Vol. 107, No. 6. pp. 893-897.
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