McLaughlin Tracey, Abbasi Fahim, Lamendola Cindy, Frayo R Scott, Cummings David E
Division of Endocrinology, University of Washington, Veterans Affairs Puget Sound Health Care System, Seattle, Washington 98108, USA.
J Clin Endocrinol Metab. 2004 Apr;89(4):1630-5. doi: 10.1210/jc.2003-031572.
Ghrelin, an orexigenic hormone that may play a role in body weight regulation, is reduced in states of obesity. Because obesity is associated with insulin resistance and compensatory hyperinsulinemia, we determined whether these metabolic characteristics were independently associated with suppressed ghrelin concentrations. To investigate this hypothesis, using steady-state plasma glucose concentrations, we identified 20 insulin-resistant (IR) and 20 insulin-sensitive (IS) individuals who were equally obese. The mean body mass indexes were 32.5 +/- 0.4 and 32.0 +/- 0.4 kg/m(2) for the IR and IS groups, respectively. Fasting insulin concentrations were 19.5 and 7.4 micro U/ml (P < 0.001), respectively. Ghrelin concentrations were suppressed in the IR group (252 +/- 19 pg/ml) relative to the IS group (412 +/- 35 pg/ml; P < 0.001). Ghrelin correlated inversely with both insulin resistance (r = -0.64; P < 0.001) and fasting insulin concentration (r = -0.58; P < 0.001). Multivariate analysis confirmed that both insulin resistance and hyperinsulinemia independently predicted low ghrelin concentrations. Our results demonstrate that in obese individuals, insulin resistance and hyperinsulinemia are inversely associated with ghrelin concentrations. Thus, insulin resistance or related metabolic abnormalities may constitute part of a feedback mechanism by which body weight is regulated in humans.
胃饥饿素是一种可能在体重调节中起作用的促食欲激素,在肥胖状态下会减少。由于肥胖与胰岛素抵抗和代偿性高胰岛素血症相关,我们确定了这些代谢特征是否与胃饥饿素浓度受抑制独立相关。为了研究这一假设,我们利用稳态血浆葡萄糖浓度,确定了20名胰岛素抵抗(IR)和20名胰岛素敏感(IS)的个体,他们的肥胖程度相同。IR组和IS组的平均体重指数分别为32.5±0.4和32.0±0.4kg/m²。空腹胰岛素浓度分别为19.5和7.4微单位/毫升(P<0.001)。相对于IS组(412±35皮克/毫升;P<0.001),IR组的胃饥饿素浓度受到抑制(252±19皮克/毫升)。胃饥饿素与胰岛素抵抗(r=-0.64;P<0.001)和空腹胰岛素浓度(r=-0.58;P<0.001)均呈负相关。多变量分析证实,胰岛素抵抗和高胰岛素血症均独立预测胃饥饿素浓度较低。我们的结果表明,在肥胖个体中,胰岛素抵抗和高胰岛素血症与胃饥饿素浓度呈负相关。因此,胰岛素抵抗或相关代谢异常可能构成人类体重调节反馈机制的一部分。