Buntain H M, Schluter P J, Bell S C, Greer R M, Wong J C H, Batch J, Lewindon P, Wainwright C E
Department of Respiratory Medicine, Royal Children's Hospital, Herston, QLD 4029, Australia.
Thorax. 2006 Feb;61(2):146-54. doi: 10.1136/thx.2005.046516. Epub 2005 Dec 29.
A study was undertaken to observe the gains in bone mass in children and adolescents with cystic fibrosis (CF) over 24 months and to examine the relationship between areal bone mineral density (aBMD) and associated clinical parameters including physical activity, nutrition, and 25-hydroxyvitamin D (25OHD).
Areal BMD of the total body (TB), lumbar spine (LS), and total femoral neck (FNt) were repeatedly measured in 85 subjects aged 5-18 years with CF and 100 age and sex matched controls over 2 years. At each visit anthropometric variables, nutritional parameters, pubertal status, disease severity, physical activity, dietary calcium, caloric intake, and serum 25OHD were assessed and related to aBMD.
After adjusting for age, sex, and height Z-score, gains in LS aBMD in children (5-10 years) and TB and FNt aBMD in adolescents (11-18 years) with CF were significantly less than in controls. Lean tissue mass was significantly associated with TB and LS aBMD gains in children and adolescents and explained a significant proportion of the aBMD deficit observed. Lung function parameters were significantly associated with aBMD gains in adolescents with CF.
Inadequate bone mass accrual during childhood and adolescence contributes to the low bone mass observed in adults with CF. Accounting for the height discrepancy which is frequently observed in those with CF, in addition to age and sex, is important when assessing low bone mass in children and adolescents with CF. To optimise an individual's potential to acquire maximal bone mass, it is necessary to maximise nutritional status and limit the progression of chronic suppurative lung disease.
开展了一项研究,以观察囊性纤维化(CF)儿童和青少年在24个月内的骨量增加情况,并研究面积骨密度(aBMD)与包括身体活动、营养和25-羟基维生素D(25OHD)在内的相关临床参数之间的关系。
对85名年龄在5至18岁的CF患者和100名年龄及性别匹配的对照者进行了为期2年的全身(TB)、腰椎(LS)和股骨颈(FNt)的面积骨密度重复测量。每次访视时,评估人体测量变量、营养参数、青春期状态、疾病严重程度、身体活动、膳食钙、热量摄入和血清25OHD,并将其与aBMD相关联。
在调整年龄、性别和身高Z评分后,CF儿童(5至10岁)的LS aBMD增加以及CF青少年(11至18岁)的TB和FNt aBMD增加均显著低于对照组。瘦组织质量与儿童和青少年的TB和LS aBMD增加显著相关,并解释了观察到的aBMD不足的很大一部分。肺功能参数与CF青少年的aBMD增加显著相关。
儿童和青少年时期骨量积累不足导致CF成年患者骨量较低。在评估CF儿童和青少年的低骨量时,除年龄和性别外,考虑CF患者中经常观察到的身高差异也很重要。为了优化个体获得最大骨量的潜力,有必要最大限度地提高营养状况并限制慢性化脓性肺病的进展。