Division of Endocrinology, Department of Pediatrics, University of Virginia School of Medicine, Charlottesville, Virginia.
Center for Research in Reproduction, University of Virginia School of Medicine, Charlottesville, Virginia.
J Clin Endocrinol Metab. 2018 Jul 1;103(7):2571-2582. doi: 10.1210/jc.2018-00131.
Peripubertal obesity is associated with variable hyperandrogenemia, but precise mechanisms remain unclear.
To assess insulin resistance, hyperinsulinemia, and LH roles in peripubertal obesity-associated hyperandrogenemia.
Cross-sectional analysis.
Academic clinical research unit.
Eleven obese (body mass index for age ≥95%) peripubertal girls.
Blood samples were taken during a mixed-meal tolerance test (1900 to 2100), overnight (2100 to 0700), while fasting (0700 to 0900), and during an 80 mU/m2/min hyperinsulinemic-euglycemic clamp (0900 to 1100).
The dependent variable was morning free testosterone level; independent variables were insulin sensitivity index (ISI), estimated 24-hour insulin, and estimated 24-hour LH levels.
All participants demonstrated insulin resistance and hyperinsulinemia. ISI, but not estimated 24-hour insulin level, correlated positively with morning free testosterone level when correcting for estimated 24-hour LH level and Tanner stage (rs = 0.68, P = 0.046). The correlation between estimated 24-hour LH and free testosterone levels approached significance after adjusting for estimated 24-hour insulin level and Tanner stage (rs = 0.63, P = 0.067). Estimated 24-hour insulin level did not correlate with free testosterone level after adjusting for estimated 24-hour LH level and Tanner stage (rs = 0.47, P = 0.20).
In insulin-resistant obese girls with hyperinsulinemia, free testosterone levels correlated positively with insulin sensitivity and, likely, circulating LH concentrations but not with circulating insulin levels. In the setting of relatively uniform hyperinsulinemia, variable steroidogenic-cell insulin sensitivity may correlate with metabolic insulin sensitivity and contribute to variable free testosterone concentrations.
青春期前肥胖与可变的高雄激素血症有关,但确切的机制尚不清楚。
评估胰岛素抵抗、高胰岛素血症和 LH 在青春期前肥胖相关高雄激素血症中的作用。
横断面分析。
学术临床研究单位。
11 名肥胖(年龄体重指数≥95%)青春期前女孩。
在混合餐耐量试验期间(1900 至 2100)、过夜(2100 至 0700)、禁食期间(0700 至 0900)和 80 mU/m2/min 高胰岛素正常血糖钳夹期间(0900 至 1100)采集血样。
因变量为清晨游离睾酮水平;自变量为胰岛素敏感指数(ISI)、估计 24 小时胰岛素和估计 24 小时 LH 水平。
所有参与者均表现出胰岛素抵抗和高胰岛素血症。ISI,但不是估计的 24 小时胰岛素水平,在校正估计的 24 小时 LH 水平和 Tanner 阶段后,与清晨游离睾酮水平呈正相关(rs=0.68,P=0.046)。在校正估计的 24 小时 LH 和游离睾酮水平后,估计的 24 小时 LH 与游离睾酮水平的相关性接近显著(rs=0.63,P=0.067)。在校正估计的 24 小时 LH 水平和 Tanner 阶段后,估计的 24 小时胰岛素水平与游离睾酮水平无相关性(rs=0.47,P=0.20)。
在胰岛素抵抗的肥胖、高胰岛素血症的青春期前女孩中,游离睾酮水平与胰岛素敏感性呈正相关,可能与循环 LH 浓度相关,但与循环胰岛素水平无关。在相对一致的高胰岛素血症环境下,可变的类固醇生成细胞胰岛素敏感性可能与代谢胰岛素敏感性相关,并导致可变的游离睾酮浓度。