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High dose vitamin D therapy for chronic pain in children and adolescents with sickle cell disease: results of a randomized double blind pilot study
被引:52
|作者:
Osunkwo, Ifeyinwa
[1
,2
]
Ziegler, Thomas R.
[3
]
Alvarez, Jessica
[3
]
McCracken, Courtney
[2
]
Cherry, Korin
[1
]
Osunkwo, Chinyere E.
[1
]
Ofori-Acquah, Solomon F.
[1
,2
]
Ghosh, Samit
[2
]
Ogunbobode, Adeolu
[2
]
Rhodes, Jim
[1
]
Eckman, James R.
[4
,5
]
Dampier, Carlton
[1
,2
]
Tangpricha, Vin
[3
]
机构:
[1] Ctr Childrens Healthcare Atlanta, Aflac Canc & Blood Disorders, Atlanta, GA USA
[2] Emory Univ, Sch Med, Dept Pediat, Atlanta, GA USA
[3] Emory Univ, Sch Med, Div Endocrinol Metab & Lipids, Atlanta, GA USA
[4] Emory Univ, Sch Med, Dept Hematol Oncol, Winship Canc Inst, Atlanta, GA USA
[5] Georgia Comprehens Sickle Cell Ctr Grady Mem Hosp, Atlanta, GA USA
关键词:
vitamin D;
chronic pain;
sickle cell;
paediatrics;
quality of life;
QUALITY-OF-LIFE;
D DEFICIENCY;
PREVALENCE;
ADULTS;
D O I:
10.1111/bjh.12019
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
We report results of a pilot study of high-dose vitamin D in sickle cell disease (SCD). Subjects were given a 6-week course of oral high-dose cholecalciferol (40 000-100 000 IU per week) or placebo and monitored prospectively for a period of six months. Vitamin D insufficiency and deficiency was present at baseline in 82.5% and 52.5% of subjects, respectively. Subjects who received high-dose vitamin D achieved higher serum 25-hydroxyvitamin D, experienced fewer pain days per week, and had higher physical activity quality-of-life scores. These findings suggest a potential benefit of vitamin D in reducing the number of pain days in SCD. Larger prospective studies with longer duration are needed to confirm these effects.
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页码:211 / 215
页数:5
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