A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Endothelial function in long-term survivors of childhood acute lymphoblastic leukemia: Effects of a home-based exercise program
Alaotsikko: Effects of a home-based exercise program
Tekijät: Jarvela LS, Niinikoski H, Heinonen OJ, Lahteenmaki PM, Arola M, Kemppainen J
Kustantaja: WILEY-BLACKWELL
Kustannuspaikka: Hoboken, N.J.
Julkaisuvuosi: 2013
Journal: Pediatric Blood and Cancer
Tietokannassa oleva lehden nimi: PEDIATRIC BLOOD & CANCER
Lehden akronyymi: PEDIATR BLOOD CANCER
Numero sarjassa: 9
Vuosikerta: 60
Numero: 9
Aloitussivu: 1546
Lopetussivu: 1551
Sivujen määrä: 6
ISSN: 1545-5009
DOI: https://doi.org/10.1002/pbc.24565
Tiivistelmä
Background The risk for cardiovascular disease (CVD) is increased in long-term survivors of childhood acute lymphoblastic leukemia (ALL). Chemotherapy may have direct toxic effects on vascular endothelium, potentially increasing the significance of endothelial dysfunction in the development of CVD in ALL survivors. Endothelial structure and function can be measured with carotid intima media thickness (IMT) and brachial flow mediated dilation (FMD). IMT and FMD are intermediate markers of CVD. We studied endothelial function and the effects of an exercise program on vascular endothelium in long-term survivors of childhood ALL. Procedure Twenty-one 16-30 year old long-term survivors of ALL (age at diagnosis 16 years) and 21 healthy controls were studied at baseline, and 17 of the ALL survivors participated in a 16 week home-based exercise program. IMT and FMD were studied before and after the exercise program. Results At baseline, the ALL survivors had impaired overall FMD response (FMDauc, P=0.02). FMDmax(%) was 22% lower (P=0.06) and FMD at 40seconds 44% lower (P=0.01) compared to healthy controls. After the exercise program, FMD at 40seconds (P<0.01) and IMT (P=0.02) improved. The mean overall FMD response increased by 25% after the exercise program, but this change was not statistically significant (P=0.27). Conclusions Our results show that the excess burden of CVD morbidity in this population may possibly be alleviated by simple means. The importance of physical activity on the health of childhood ALL survivors should be emphasized. Longer, controlled studies are needed to confirm our findings. Pediatr Blood Cancer 2013;160:1546-1551. (c) 2013 Wiley Periodicals, Inc.
Background The risk for cardiovascular disease (CVD) is increased in long-term survivors of childhood acute lymphoblastic leukemia (ALL). Chemotherapy may have direct toxic effects on vascular endothelium, potentially increasing the significance of endothelial dysfunction in the development of CVD in ALL survivors. Endothelial structure and function can be measured with carotid intima media thickness (IMT) and brachial flow mediated dilation (FMD). IMT and FMD are intermediate markers of CVD. We studied endothelial function and the effects of an exercise program on vascular endothelium in long-term survivors of childhood ALL. Procedure Twenty-one 16-30 year old long-term survivors of ALL (age at diagnosis 16 years) and 21 healthy controls were studied at baseline, and 17 of the ALL survivors participated in a 16 week home-based exercise program. IMT and FMD were studied before and after the exercise program. Results At baseline, the ALL survivors had impaired overall FMD response (FMDauc, P=0.02). FMDmax(%) was 22% lower (P=0.06) and FMD at 40seconds 44% lower (P=0.01) compared to healthy controls. After the exercise program, FMD at 40seconds (P<0.01) and IMT (P=0.02) improved. The mean overall FMD response increased by 25% after the exercise program, but this change was not statistically significant (P=0.27). Conclusions Our results show that the excess burden of CVD morbidity in this population may possibly be alleviated by simple means. The importance of physical activity on the health of childhood ALL survivors should be emphasized. Longer, controlled studies are needed to confirm our findings. Pediatr Blood Cancer 2013;160:1546-1551. (c) 2013 Wiley Periodicals, Inc.
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