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Genetic studies of leptin concentrations implicate leptin in the regulation of early adiposity

journal contribution
posted on 2024-07-25, 15:48 authored by Hanieh YaghootkarHanieh Yaghootkar, Y. Zhang, C.N. Spracklen, T. Karaderi, L.O. Huang, J. Bradfield, C. Schurmann, R.S. Fine, M.H. Preuss, Z. Kutalik, L.B.L. Wittemans, Y. Lu, S. Metz, S.M. Willems, R. Li-Gao, N. Grarup, S. Wang, S. Molnos, A.A. Sandoval-Zárate, M.A. Nalls, L.A. Lange, J. Haesser, X. Guo, L.-P. Lyytikäinen, M.F. Feitosa, C.M. Sitlani, C. Venturini, A. Mahajan, T. Kacprowski, C.A. Wang, D.I. Chasman, N. Amin, L. Broer, N. Robertson, K.L. Young, M. Allison, P.L. Auer, M. Blüher, J.B. Borja, J. Bork-Jensen, G.D. Carrasquilla, P. Christofidou, A. Demirkan, C.A. Doege, M.E. Garcia, M. Graff, K. Guo, H. Hakonarson, J. Hong, Y.-D.I. Chen, R. Jackson, H. Jakupovic, P. Jousilahti, A.E. Justice, M. Kähönen, J.R. Kizer, J. Kriebel, C.A. Leduc, J. Li, L. Lind, J. Luan, D.A. Mackey, M. Mangino, S. Männistö, J.F.M. Carli, C. Medina-Gomez, D.O. Mook-Kanamori, A.P. Morris, R. de, M. Nauck, I. Prokic, C.E. Pennell, A.D. Pradhan, B.M. Psaty, O.T. Raitakari, R.A. Scott, T. Skaaby, K. Strauch, K.D. Taylor, A. Teumer, A.G. Uitterlinden, Y. Wu, J. Yao, M. Walker, K.E. North, P. Kovacs, M.A. Ikram, C.M. van, P.M. Ridker, S. Lye, G. Homuth, E. Ingelsson, T.D. Spector, B. McKnight, M.A. Province, T. Lehtimäki, L.S. Adair, J.I. Rotter, A.P. Reiner, J.G. Wilson, T.B. Harris, S. Ripatti, H. Grallert, J.B. Meigs, V. Salomaa, T. Hansen, K.W. van, N.J. Wareham, S.F.A. Grant, C. Langenberg, T.M. Frayling, C.M. Lindgren, K.L. Mohlke, R.L. Leibel, R.J.F. Loos, T.O. Kilpeläinen

Leptin influences food intake by informing the brain about the status of body fat stores. Rare LEP mutations associated with congenital leptin deficiency cause severe early-onset obesity that can be mitigated by admin-istering leptin. However, the role of genetic regulation of leptin in polygenic obesity remains poorly understood. We performed an exome-based analysis in up to 57,232 individuals of diverse ancestries to identify genetic variants that influence adiposity-adjusted leptin concen-trations. We identify five novel variants, including four missense variants, in LEP, ZNF800, KLHL31, and ACTL9, and one intergenic variant near KLF14. The missense variant Val94Met (rs17151919) in LEP was common in individuals of African ancestry only, and its association with lower leptin concentrations was specific to this ancestry (P = 2 × 10-16, n = 3,901). Using in vitro analyses, we show that the Met94 allele decreases leptin secretion. We also show that the Met94 allele is associated with higher BMI in young African-ancestry children but not in adults, suggesting that leptin regulates early adiposity. © 2020 by the American Diabetes Association.

History

School affiliated with

  • School of Chemistry (Research Outputs)

Publication Title

Diabetes

Volume

69

Issue

12

Pages/Article Number

2806-2818

Publisher

American Diabetes Association Inc.

ISSN

121797

Date Accepted

2020-09-09