Literature DB >> 9972187

Elevated resting energy expenditure in adolescents with sickle cell anemia.

L E Kopp-Hoolihan1, M D van Loan, W C Mentzer, M B Heyman.   

Abstract

OBJECTIVE: To assess the reliability of standard prediction equations in estimating resting energy expenditure (REE) values in adolescents with sickle cell anemia. SUBJECTS/
DESIGN: Body composition and metabolic measurements were performed in 8 adolescents, aged 11 to 18 years, with homozygous sickle cell anemia. REE was measured by indirect calorimetry under standard conditions, and measurements were compared with 4 prediction formulas (Harris-Benedict, Schofield, Mayo Clinic, and Food and Agriculture Organization/World Health Organization/United Nations University). Fat-free mass was measured to assess REE per unit of actively metabolizing tissue. Fat-free mass was expressed as a mean of values obtained by densitometry, deuterium dilution, 40K-counting, and total body electrical conductivity. STATISTICAL ANALYSES: Repeated measures analysis of variance was performed to determine whether measured REE values and predicted values differed. The Fischer test was used to identify which predicted values differed significantly from the measured REE.
RESULTS: All 4 prediction formulas significantly underestimated REE. Group mean values for the prediction formulas ranged from 83% to 89% of the measured value. REE averaged 47.7 +/- 10.0 kcal/kg fat-free mass per day, which is 30% to 50% higher than reported values in healthy adolescent populations.
CONCLUSIONS: These data suggest that REE is elevated in adolescents with sickle cell anemia. Standard equations used to predict REE are unreliable in these patients. APPLICATIONS: REE in patients with sickle cell anemia is best determined by indirect or direct measurement of energy expenditure. Clinically useful formulas to estimate REE should be developed for patients with conditions, including sickle cell anemia, where the metabolic rate may be altered.

Entities:  

Mesh:

Year:  1999        PMID: 9972187     DOI: 10.1016/S0002-8223(99)00047-4

Source DB:  PubMed          Journal:  J Am Diet Assoc        ISSN: 0002-8223


  4 in total

1.  Letter to the Editor Concerning: Sharma, P.; McCarty, T. R.; Yadav, S.; Ngu, J. N.; and Njei, B. (2019). Impact of Bariatric Surgery on Outcomes of Patients with Sickle Cell Disease: a Nationwide Inpatient Sample Analysis, 2004-2014. Obesity Surgery, 1-8.

Authors:  Stéphanie Ngo; Marinos Fysekidis; Régis Cohen; Abdallah Al-Salameh
Journal:  Obes Surg       Date:  2019-08       Impact factor: 4.129

Review 2.  Prevalence of vitamin D deficiency in sickle cell disease: a systematic review.

Authors:  Vikki G Nolan; Kerri A Nottage; Elliott W Cole; Jane S Hankins; James G Gurney
Journal:  PLoS One       Date:  2015-03-03       Impact factor: 3.240

3.  SOCIOECONOMIC AND NUTRITIONAL CHARACTERISTICS OF CHILDREN AND ADOLESCENTS WITH SICKLE CELL ANEMIA: A SYSTEMATIC REVIEW.

Authors:  Amanda Cristina da Silva de Jesus; Tulio Konstantyner; Ianna Karolina Véras Lôbo; Josefina Aparecida Pellegrini Braga
Journal:  Rev Paul Pediatr       Date:  2018 Oct-Dec

4.  Insulin Sensitivity, Inflammation, and Basal Metabolic Rate in Adults with Sickle Cell Anemia.

Authors:  Kehinde Sola Akinlade; Ayodeji Samuel Kumuyi; Sheu Kadiri Rahamon; John Ayodele Olaniyi
Journal:  Int J Appl Basic Med Res       Date:  2018 Apr-Jun
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.