Original Article

Obesity Research (2004) 12, 1060–1066; doi: 10.1038/oby.2004.133

The Val103Ile Polymorphism of Melanocortin-4 Receptor Regulates Energy Expenditure and Weight Gain**

Jarno Rutanen*, Jussi Pihlajamäki*, Pauli Karhapää*, Ilkka Vauhkonen*, Johanna Kuusisto*, Leena Moilanen Mykkänen* and Markku Laakso*

*Department of Medicine, University of Kuopio, Kuopio, Finland

Correspondence: Jussi Pihlajamäki Department of Medicine, Kuopio University Hospital, PB 1777, 70211 Kuopio, Finland. E-mail: pihlajam@uku.fi

**The costs of publication of this article were defrayed, in part, by the payment of page charges. This article must, therefore, be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Received 2 September 2003; Revised  00; Accepted 17 May 2004.

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Abstract

Objective: The melanocortin-4 receptor (MC4R) regulates energy intake. On the basis of animal studies, it may also regulate energy expenditure.

Research Methods and Procedures: The effect of the Val103Ile polymorphism of the MC4R gene on energy metabolism was studied in 229 middle-aged nondiabetic subjects (Group 1, age 51.2 plusminus 9.8 years, BMI 26.8 plusminus 4.5 kg/m2) and on weight gain in 1013 elderly subjects (Group 2, age 69.9 plusminus 2.9 years, BMI 27.4 plusminus 4.1 kg/m2) during a 3.5-year follow-up study. In Group 1, insulin sensitivity, energy expenditure, and substrate oxidation were measured with the hyperinsulinemic euglycemic clamp combined with indirect calorimetry.

Results: In Group 1, the Val103Ile genotype was associated with high rates of energy expenditure (63.42 plusminus 13.40 in eight subjects with the Val103Ile genotype vs. 59.86 plusminus 7.33 J/kg per minute in 221 subjects with the Val103Val genotype, p = 0.007), high rates of glucose oxidation (8.90 plusminus 6.15 vs. 6.07 plusminus 4.38 mumol/kg per minute, p = 0.020), and low levels of free fatty acids (0.45 plusminus 0.18 vs. 0.56 plusminus 0.23 mM, p = 0.029) in the fasting state, and with high rates of glucose oxidation during the clamp (18.88 plusminus 4.63 vs. 17.60 plusminus 3.24 mumol/kg per minute, p = 0.031). In Group 2, the 103Ile allele was associated with an increase in weight gain during the follow-up (0.78 plusminus 3.98 vs. -0.82 plusminus 3.98 kg, p = 0.038).

Discussion: The Val103Ile polymorphism of the MC4R gene is associated with energy expenditure in humans. Furthermore, it may associate with glucose oxidation, free fatty acid levels, and weight gain.

Keywords:

energy metabolism, glucose oxidation, central nervous system, hyperinsulinemic euglycemic clamp, insulin sensitivity

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