Functional Magnetic Resonance Imaging Analysis of Food-Related Brain Activity in Patients with Lipodystrophy Undergoing Leptin Replacement Therapy

Author:

Aotani Daisuke12,Ebihara Ken12,Sawamoto Nobukatsu3,Kusakabe Toru1,Aizawa-Abe Megumi12,Kataoka Sachiko1,Sakai Takeru1,Iogawa Hitomi1,Ebihara Chihiro1,Fujikura Junji1,Hosoda Kiminori123,Fukuyama Hidenao3,Nakao Kazuwa1

Affiliation:

1. Department of Medicine and Clinical Science (D.A., K.E., T.K., M.A.-A., S.K., T.S., H.I., C.E., J.F., K.H., K.N.), Kyoto University Graduate School of Medicine, Kyoto 606-8507, Japan

2. Department of Experimental Therapeutics (D.A., K.E., M.A.-A., K.H.), Translational Research Center, Kyoto University Hospital; Kyoto 606-8507, Japan

3. Kyoto University Graduate School of Medicine, Human Brain Research Center (N.S., H.F.), Kyoto 606-8507, Japan

Abstract

Abstract Context: Lipodystrophy is a disease characterized by a paucity of adipose tissue and low circulating concentrations of adipocyte-derived leptin. Leptin-replacement therapy improves eating and metabolic disorders in patients with lipodystrophy. Objective: The aim of the study was to clarify the pathogenic mechanism of eating disorders in lipodystrophic patients and the action mechanism of leptin on appetite regulation. Subjects and Interventions: We investigated food-related neural activity using functional magnetic resonance imaging in lipodystrophic patients with or without leptin replacement therapy and in healthy controls. We also measured the subjective feelings of appetite. Results: Although there was little difference in the enhancement of neural activity by food stimuli between patients and controls under fasting, postprandial suppression of neural activity was insufficient in many regions of interest including amygdala, insula, nucleus accumbens, caudate, putamen, and globus pallidus in patients when compared with controls. Leptin treatment effectively suppressed postprandial neural activity in many of these regions of interest, whereas it showed little effect under fasting in patients. Consistent with these results, postprandial formation of satiety feeling was insufficient in patients when compared with controls, which was effectively reinforced by leptin treatment. Conclusions: This study demonstrated the insufficiency of postprandial suppression of food-related neural activity and formation of satiety feeling in lipodystrophic patients, which was effectively restored by leptin. The findings in this study emphasize the important pathological role of leptin in eating disorders in lipodystrophy and provide a clue to understanding the action mechanism of leptin in human, which may lead to development of novel strategies for prevention and treatment of obesity.

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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