Hyperphagia, Severe Obesity, Impaired Cognitive Function, and Hyperactivity Associated With Functional Loss of One Copy of the Brain-Derived Neurotrophic Factor (BDNF) Gene
- Juliette Gray1,
- Giles S.H. Yeo1,
- James J. Cox2,
- Jenny Morton3,
- Anna-Lynne R. Adlam4,
- Julia M. Keogh1,
- Jack A. Yanovski5,
- Areeg El Gharbawy5,
- Joan C. Han5,
- Y.C. Loraine Tung1,
- John R. Hodges4,
- F. Lucy Raymond2,
- Stephen O’Rahilly1 and
- I. Sadaf Farooqi1
- 1University Department of Clinical Biochemistry, Cambridge Institute for Medical Research, Addenbrooke’s Hospital, Cambridge, U.K
- 2University Department of Medical Genetics, Cambridge Institute for Medical Research, Addenbrooke’s Hospital, Cambridge, U.K
- 3West Midlands Regional Genetics Service, Birmingham Women’s Hospital, Birmingham, U.K
- 4Medical Research Council, Cognition and Brain Sciences Unit, and the Department of Clinical Neurosciences, Addenbrooke’s Hospital, Cambridge, U.K
- 5Unit on Growth and Obesity, Developmental Endocrinology Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland
- Address correspondence and reprint requests to I. Sadaf Farooqi, University Department of Clinical Biochemistry, Cambridge Institute for Medical Research, Addenbrooke’s Hospital, Cambridge, CB2 2XY, U.K. E-mail: isf20{at}cam.ac.uk
Abstract
The neurotrophin brain-derived neurotrophic factor (BDNF) inhibits food intake, and rodent models of BDNF disruption all exhibit increased food intake and obesity, as well as hyperactivity. We report an 8-year-old girl with hyperphagia and severe obesity, impaired cognitive function, and hyperactivity who harbored a de novo chromosomal inversion, 46,XX,inv(11)(p13p15.3), a region encompassing the BDNF gene. We have identified the proximal inversion breakpoint that lies 850 kb telomeric of the 5′ end of the BDNF gene. The patient’s genomic DNA was heterozygous for a common coding polymorphism in BDNF, but monoallelic expression was seen in peripheral lymphocytes. Serum concentration of BDNF protein was reduced compared with age- and BMI-matched subjects. Haploinsufficiency for BDNF was associated with increased ad libitum food intake, severe early-onset obesity, hyperactivity, and cognitive impairment. These findings provide direct evidence for the role of the neurotrophin BDNF in human energy homeostasis, as well as in cognitive function, memory, and behavior.
- BAC, bacterial artificial chromosome
- BDNF, brain-derived neurotrophic factor
- FISH, fluorescence in situ hybridization
- TrkB, tropomyosin-related kinase B
Footnotes
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Additional information for this article can be found in an online appendix at http://diabetes.diabetesjournals.org.
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- Accepted August 21, 2006.
- Received April 24, 2006.
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