King Susannah J, Nyulasi Ibolya B, Bailey Michael, Kotsimbos Tom, Wilson John W
Nutrition Department, Alfred Hospital, Commercial Road, Melbourne, Victoria 3004, Australia; Department of Medicine, Monash University, Alfred Hospital, Commercial Road, Melbourne, Victoria 3004, Australia; Department of Dietetics and Human Nutrition, La Trobe University, Bundoora, Victoria 3086, Australia.
Nutrition Department, Alfred Hospital, Commercial Road, Melbourne, Victoria 3004, Australia; Department of Medicine, Monash University, Alfred Hospital, Commercial Road, Melbourne, Victoria 3004, Australia.
Clin Nutr. 2014 Feb;33(1):150-5. doi: 10.1016/j.clnu.2013.04.012. Epub 2013 Apr 24.
BACKGROUND & AIMS: Malnutrition is associated with poorer outcome in cystic fibrosis (CF). This follow-up study aimed to document nutritional status changes, including fat-free mass (FFM), in adults with CF; and to identify predictors of FFM loss.
Fifty-eight non-transplanted CF adults (mean ± SD forced expiratory volume in one second (FEV1) 63.7 ± 21.4%predicted; mean ± SD age 30.3 ± 7.7years at baseline) were studied at baseline and 3.6 ± 0.4 years later. Body composition was measured using dual-energy X-ray absorptiometry. At follow-up, blood was analysed for interleukin-6 and tumour necrosis factor-α (TNF-α) on three occasions over six months and averaged for each participant. Associations with annual percentage change in FFM (ann%ΔFFM), including cytokines, CF genotype and annual change in FEV1%predicted (annΔFEV1%), were determined.
Mean FFM was 49.5 ± 8.8 kg at baseline and 49.6 ± 8.9 kg at follow-up (p = 0.66). Ann%ΔFFM ranged from -2.0 to +3.6%. FEV1%predicted declined by 1.2 ± 2.4% per year. Forty percent of participants had elevated average interleukin-6 levels. Ann%ΔFFM was negatively correlated with interleukin-6 levels (rho -0.34, p = 0.008), but not TNF-α or annΔFEV1%. F508DEL homozygote or heterozygote participants had greater FFM loss than those carrying no F508DEL allele (p = 0.01).
Higher serum interleukin-6 and presence of the F508DEL mutation, but not TNF-α, were associated with FFM loss in adults with CF.
营养不良与囊性纤维化(CF)患者较差的预后相关。这项随访研究旨在记录成年CF患者的营养状况变化,包括去脂体重(FFM);并确定FFM丢失的预测因素。
对58名未接受移植的成年CF患者进行研究,基线时平均一秒用力呼气容积(FEV1)为预测值的63.7±21.4%;基线时平均年龄为30.3±7.7岁。在基线时和3.6±0.4年后对患者进行研究。使用双能X线吸收法测量身体成分。随访时,在六个月内分三次对血液中的白细胞介素-6和肿瘤坏死因子-α(TNF-α)进行分析,并计算每位参与者的平均值。确定了包括细胞因子、CF基因型和预测FEV1%的年变化率(annΔFEV1%)与FFM年百分比变化(ann%ΔFFM)之间的关联。
基线时平均FFM为49.5±8.8kg,随访时为49.6±8.9kg(p=0.66)。Ann%ΔFFM范围为-2.0至+3.6%。预测FEV1%每年下降1.2±2.4%。40%的参与者平均白细胞介素-6水平升高。Ann%ΔFFM与白细胞介素-6水平呈负相关(rho=-0.34,p=0.008),但与TNF-α或annΔFEV1%无关。F508DEL纯合子或杂合子参与者的FFM丢失比未携带F508DEL等位基因的参与者更多(p=0.01)。
较高的血清白细胞介素-6水平和F508DEL突变的存在与成年CF患者的FFM丢失有关,而TNF-α则无关。