期刊
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
卷 56, 期 9, 页码 898-904出版社
WILEY
DOI: 10.1111/dmcn.12462
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资金
- Children's Hospital of Philadelphia Ketogenic Diet Team
- Clinical and Translational Research Center team
- NIH [RR-K23-16074]
- Clinical and Translational Research Center [UL1RR024134]
- Nutrition Center at the Children's Hospital of Philadelphia
- Ste-Justine University Hospital Center, Montreal, Canada
AIM The long-term effects of the ketogenic diet, a high fat diet for treating intractable epilepsy, on resting energy expenditure (REE) are unknown. The aim of this study was to evaluate the impact of 15 months of ketogenic diet treatment on growth and REE in children with intractable epilepsy. METHOD Growth, body composition, and REE were assessed at baseline, 3 months and 15 months in 24 children (14 males, 10 females; mean age 5y 6mo [SD 26mo], range 7mo-6y 5mo), 10 with cerebral palsy [CP]). Fifteen were identified as ketogenic diet responders at 3 months and continued on the ketogenic diet until 15 months. These were compared to 75 healthy children (43 males, 32 females; mean age 6y 3mo [SD 21mo] age range 2-9y). REE was expressed as percentage predicted, growth as height (HAz) and weight (WAz) z-scores, and body composition as fat and fat free mass (FFM). RESULTS HAz declined -0.2 and -0.6 from baseline to 3 months and 15 months respectively (p=0.001), while WAz was unchanged. In ketogenic diet responders, FFM, age and CP diagnosis predicted REE (overall R-2=0.76, p<0.001) and REE did not change. REE adjusted for FFM was lower (p<0.01) in children with CP at baseline (mean [standard error], -143[51] kcals/d) and 15 months (-198[53] kcals/d) compared to the healthy children. INTERPRETATION After 15 months of the ketogenic diet, linear growth status declined while weight status and REE were unchanged. REE remained reduced in children with CP.
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