de Koning Lisanne, Warnink-Kavelaars Jessica, van Rossum Marion, Limmen Selina, Van der Looven Ruth, Muiño-Mosquera Laura, van der Hulst Annelies, Oosterlaan Jaap, Rombaut Lies, Engelbert Raoul
Center of Expertise Urban Vitality, Faculty of Health, University of Applied Sciences Amsterdam, Amsterdam, Netherlands.
Department of Rehabilitation Medicine, Amsterdam UMC Location University of Amsterdam, Amsterdam, Netherlands.
Front Pediatr. 2023 Mar 17;11:1057070. doi: 10.3389/fped.2023.1057070. eCollection 2023.
Health problems in patients with heritable connective tissue disorders (HCTD) are diverse and complex and might lead to lower physical activity (PA) and physical fitness (PF). This study aimed to investigate the PA and PF of children with heritable connective tissue disorders (HCTD).
PA was assessed using an accelerometer-based activity monitor (ActivPAL) and the mobility subscale of the Pediatric Evaluation of Disability Inventory Computer Adaptive Test (PEDI-CAT). PF was measured in terms of cardiovascular endurance using the Fitkids Treadmill Test (FTT); maximal hand grip strength, using hand grip dynamometry (HGD) as an indicator of muscle strength; and motor proficiency, using the Bruininks-Oseretsky Test of Motor Proficiency-2 (BOTMP-2).
A total of 56 children, with a median age of 11.6 (interquartile range [IQR], 8.8-15.8) years, diagnosed with Marfan syndrome (MFS), = 37, Loeys-Dietz syndrome (LDS), = 6, and genetically confirmed Ehlers-Danlos (EDS) syndromes, = 13 (including classical EDS = 10, vascular EDS = 1, dermatosparaxis EDS = 1, arthrochalasia EDS = 1), participated. Regarding PA, children with HCTD were active for 4.5 (IQR 3.5-5.2) hours/day, spent 9.2 (IQR 7.6-10.4) hours/day sedentary, slept 11.2 (IQR 9.5-11.5) hours/day, and performed 8,351.7 (IQR 6,456.9-1,0484.6) steps/day. They scored below average (mean (standard deviation [SD]) -score -1.4 (1.6)) on the PEDI-CAT mobility subscale. Regarding PF, children with HCTD scored well below average on the FFT (mean (SD) -score -3.3 (3.2)) and below average on the HGD (mean (SD) -score -1.1 (1.2)) compared to normative data. Contradictory, the BOTMP-2 score was classified as average (mean (SD) -score.02 (.98)). Moderate positive correlations were found between PA and PF (r(39) = .378, < .001). Moderately sized negative correlations were found between pain intensity and fatigue and time spent actively (r(35) = .408, < .001 and r(24) = .395 < .001, respectively).
This study is the first to demonstrate reduced PA and PF in children with HCTD. PF was moderately positively correlated with PA and negatively correlated with pain intensity and fatigue. Reduced cardiovascular endurance, muscle strength, and deconditioning, combined with disorder-specific cardiovascular and musculoskeletal features, are hypothesized to be causal. Identifying the limitations in PA and PF provides a starting point for tailor-made interventions.
遗传性结缔组织病(HCTD)患者的健康问题多样且复杂,可能导致身体活动(PA)和身体素质(PF)降低。本研究旨在调查遗传性结缔组织病(HCTD)患儿的身体活动和身体素质。
使用基于加速度计的活动监测仪(ActivPAL)和儿童残疾评定量表计算机自适应测试(PEDI-CAT)的活动子量表评估身体活动。通过Fitkids跑步机测试(FTT)测量心血管耐力来评估身体素质;使用握力计(HGD)测量最大握力作为肌肉力量指标;使用布鲁因inks-奥塞列茨基运动技能测试-2(BOTMP-2)评估运动能力。
共有56名儿童参与,中位年龄为11.6岁(四分位间距[IQR],8.8 - 15.8岁),诊断为马凡综合征(MFS),n = 37,洛伊斯-迪茨综合征(LDS),n = 6,以及基因确诊的埃勒斯-当洛综合征(EDS),n = 13(包括经典型EDS 10例,血管型EDS 1例,皮肤松弛型EDS 1例,关节松弛型EDS 1例)。关于身体活动,HCTD患儿每天活动4.5小时(IQR 3.5 - 5.2),每天久坐9.2小时(IQR 7.6 - 10.4),每天睡眠11.2小时(IQR 9.5 - 11.5),每天步数为8351.7步(IQR 6456.9 - 10484.6)。他们在PEDI-CAT活动子量表上的得分低于平均水平(均值(标准差[SD])z得分 -1.4(1.6))。关于身体素质,与标准数据相比,HCTD患儿在FTT上的得分远低于平均水平(均值(SD)z得分 -3.3(3.2)),在HGD上的得分低于平均水平(均值(SD)z得分 -1.1(1.2))。矛盾的是,BOTMP-2得分被归类为平均水平(均值(SD)z得分0.02(0.98))。身体活动和身体素质之间存在中度正相关(r(39) = 0.378,P < 0.001)。疼痛强度和疲劳与活动时间之间存在中等程度的负相关(分别为r(35) = 0.408,P < 0.001和r(24) = 0.395,P < 0.001)。
本研究首次证明HCTD患儿的身体活动和身体素质降低。身体素质与身体活动呈中度正相关,与疼痛强度和疲劳呈负相关。心血管耐力、肌肉力量下降以及身体机能减退,再加上特定疾病的心血管和肌肉骨骼特征,被认为是其原因。识别身体活动和身体素质的局限性为量身定制的干预措施提供了起点。