Effects of Red Blood Cell Transfusion on Resting Energy Expenditure in Adolescents with Sickle Cell Anemia

Author:

Harmatz Paul1,Heyman Melvin B.2,Cunningham John3,Lee Philip D. K.45,Styles Lori6,Quirolo Keith6,Kopp‐Hoolihan Lori12,Ghiron Jim7,Hintz Raymond L.5,Vichinsky Elliott6

Affiliation:

1. Department of Gastroenterology and Nutrition Children's Hospital Oakland Oakland California

2. Department of Pediatrics University of California, San Francisco San Francisco California

3. Department of Nutrition University of Massachusetts Amherst Massachusetts

4. Department of Endocrinology Children's Hospital Oakland Oakland California

5. Department of Pediatrics Stanford University Medical School Stanford California U.S.A.

6. Department of Hematology/Oncology Children's Hospital Oakland Oakland California

7. Department of Pulmonology Children's Hospital Oakland Oakland California

Abstract

ABSTRACTBackground:Previous studies indicate that resting energy expenditure is elevated in children with sickle cell anemia, possibly caused in part by hemolysis and increased erythropoietic activity. The purpose of the present investigation was to determine whether erythrocyte transfusion normalizes resting energy expenditure in sickle cell anemia.Methods:Five adolescents with sickle cell anemia (12‐16 years old; 4 boys, 1 girl) were studied before and 1 week after erythrocyte transfusion before elective surgery or at the initial transfusion for growth failure. Resting energy expenditure was measured by indirect calorimetry, and laboratory measures were determined by routine, validated methods. Data comparisons were by nonparametric analysis.Results:After erythrocyte transfusion, total hemoglobin levels increased (difference (D = 15 g/l; p < 0.05), whereas hemoglobin S (D = ‐0.36; p < 0.05) and reticulocyte count (D = ‐0.12; p < 0.05) decreased. Mean pretransfusion resting energy expenditure was elevated to 124% above predicted levels (p < 0.05) and increased further to 134% above prediction (p < 0.05) vs. pretransfusion levels). Plasma triiodothyronine (T3) levels increased (D = 0.17 nmol/l; p < 0.05), reverse T3 (rT3) levels tended to decline (D = ‐0.04 nmol/l; p = 0.14), and rT3/T3 decreased (D = ‐0.03; p < 0.05). Plasma insulin‐like growth factor‐I (IGF‐I) levels were low‐normal before transfusion and did not change, despite the change in resting energy expenditure.Conclusions:The results confirm that resting energy expenditure is elevated in patients with sickle cell anemia. However, resting energy expenditure further increased after transfusion, despite decreased erythropoietic activity. A posttransfusion decrease in rT3/T3 may contribute to the increased resting energy expenditure. That there was no change in IGF‐I implies that the growth hormone‐IGF system is not involved in posttransfusion regulation of resting energy expenditure. Therefore, our data are not consistent with the hypothesis that increased resting energy expenditure in sickle cell anemia is directly related to erythropoietic activity. The mechanisms by which resting energy expenditure increases after transfusion in sickle cell anemia require additional investigation.

Funder

National Institutes of Health

Publisher

Wiley

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