Leptin secretory dynamics and associated disordered eating psychopathology across the weight spectrum

被引:21
作者
Baskaran, Charumathi [1 ,2 ,3 ]
Eddy, Kamryn T. [2 ,4 ]
Miller, Karen K. [3 ]
Meenaghan, Erinne [3 ]
Misra, Madhusmita [1 ,2 ,3 ]
Lawson, Elizabeth A. [3 ]
机构
[1] Massachusetts Gen Hosp Children, Pediat Endocrine Unit, 101 Merrimac,Suite 615, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, 101 Merrimac,Suite 615, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp Children, Neuroendocrine Unit, Boston, MA USA
[4] Massachusetts Gen Hosp Children, Eating Disorder Clin Res Program, Boston, MA USA
基金
美国国家卫生研究院;
关键词
POLYCYSTIC-OVARY-SYNDROME; BODY-MASS INDEX; QUESTIONNAIRE EDE-Q; ANOREXIA-NERVOSA; PLASMA LEPTIN; PEPTIDE-YY; INSULIN-RESISTANCE; CIRCULATING LEPTIN; ADOLESCENT GIRLS; ADIPOSE-TISSUE;
D O I
10.1530/EJE-15-0875
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Leptin secretory dynamics across the weight spectrum and their relationship with disordered eating psychopathology have not been studied. Our objective was to compare leptin secretory dynamics in 13 anorexia nervosa (AN), 12 overweight/obese (OB) and 12 normal-weight women using deconvolution analysis. Methods: In this cross-sectional study conducted at a tertiary referral center, serum leptin levels were obtained every 20 min from 2000 to 0800 h. Dual energy X-ray absorptiometry was used to measure percent body fat. Disordered eating psychopathology was assessed by the Eating Disorders Examination-Questionnaire (EDE-Q) and the Eating Disorders Inventory-2 (EDI-2). Results: The groups differed for basal leptin secretion (BASAL) (P=0.02). Mean leptin pulse amplitude, pulse mass, total pulsatile secretion (TPS) and area under the curve (AUC) were significantly different between groups before and after adjustment for BASAL (P<0.0001 for all). Leptin AUC correlated strongly with TPS (r=0.97, P<0.0001) and less with BASAL (r=0.35, P=0.03). On multivariate analysis, only TPS was a significant predictor of leptin AUC (P<0.0001). TPS was inversely associated with most EDE-Q and EDI-2 parameters and the associations remained significant for EDE-Q eating concern (P=0.01), and EDI-2 asceticism, ineffectiveness and social insecurity (P<0.05) after adjusting for BASAL. These relationships were not significant when controlled for percent body fat. Conclusion: Secretory dynamics of leptin differ across weight spectrum, with mean pulse amplitude, mean pulse mass and TPS being low in AN and high in OB. Pulsatile, rather than basal secretion, is the major contributor to leptin AUC. Decreased pulsatile leptin is associated with disordered eating psychopathology, possibly reflecting low percent body fat in AN.
引用
收藏
页码:503 / 512
页数:10
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