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脂肪因子和代谢风险因素对儿科康复中心肥胖儿童辍学和治疗结果的预测价值。

The Predictive Value of Adipokines and Metabolic Risk Factors for Dropouts and Treatment Outcomes in Children With Obesity Treated in a Pediatric Rehabilitation Center.

机构信息

Laboratory of Experimental Medicine and Pediatrics and Member of the Infla-Med Centre of Excellence, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.

Department of Pediatrics, Antwerp University Hospital, Edegem, Belgium.

出版信息

Front Endocrinol (Lausanne). 2022 Jun 13;13:822962. doi: 10.3389/fendo.2022.822962. eCollection 2022.

Abstract

BACKGROUND

Inpatient pediatric obesity treatments are highly effective, although dropouts and weight regain threaten long-term results. Preliminary data indicate that leptin, adiponectin, and cardiometabolic comorbidities might predict treatment outcomes. Previous studies have mainly focused on the individual role of adipokines and comorbidities, which is counterintuitive, as these risk factors tend to cluster. This study aimed to predict the dropouts and treatment outcomes by pre-treatment patient characteristics extended with cardiometabolic comorbidities (individually and in total), leptin, and adiponectin.

METHODS

Children aged 8-18 years were assessed before, immediately after and 6 months after a 12-month inpatient obesity treatment. Anthropometric data were collected at each visit. Pre-treatment lipid profiles; glucose, insulin, leptin, and adiponectin levels; and blood pressure were measured. The treatment outcome was evaluated by the change in body mass index (BMI) standard deviation score (SDS) corrected for age and sex.

RESULTS

We recruited 144 children with a mean age of 14.3 ± 2.2 years and a mean BMI of 36.7 ± 6.2 kg/m corresponding to 2.7 ± 0.4 BMI SDS. The 57 patients who dropped out during treatment and the 44 patients who dropped out during aftercare had a higher pre-treatment BMI compared to the patients who completed the treatment (mean BMI, 38.3 ± 6.8 kg/m vs 35.7 ± 5.5 kg/m) and those who completed aftercare (mean BMI, 34.6 ± 5.3 kg/m vs 37.7 ± 6.3 kg/m) (all p<0.05). Additionally, aftercare attenders were younger than non-attenders (mean age, 13.4 ± 2.3 years vs 14.9 ± 2.0, p<0.05).Patients lost on average 1.0 ± 0.4 SDS during treatment and regained 0.4 ± 0.3 SDS post-treatment corresponding to regain of 43 ± 27% (calculated as the increase in BMI SDS post-treatment over the BMI SDS lost during treatment). A higher BMI and more comorbidities inversely predicted BMI SDS reduction in linear regression (all p<0.05).The absolute BMI SDS increase after returning home was predicted by pre-treatment leptin and systolic blood pressure, whereas the post-treatment BMI SDS regain was predicted by pre-treatment age, leptin, and adiponectin levels (all p<0.05) in multivariate linear regressions.

CONCLUSION

Patients who need treatment the most are at increased risk for dropouts and weight regain, emphasizing the urgent need for interventions to reduce dropout and support inpatients after discharge. Furthermore, this study is the first to report that pre-treatment leptin and adiponectin levels predict post-treatment BMI SDS regain, requiring further research.

摘要

背景

住院儿科肥胖治疗效果显著,但辍学和体重反弹威胁着长期效果。初步数据表明瘦素、脂联素和心脏代谢合并症可能预测治疗结果。先前的研究主要集中在单独的脂联素和合并症的作用,这是反直觉的,因为这些危险因素往往会聚集在一起。本研究旨在通过治疗前患者特征(单独和总体)、瘦素和脂联素预测辍学和治疗结果。

方法

8-18 岁的儿童在住院肥胖治疗 12 个月前后进行评估。每次就诊时都采集人体测量数据。测量治疗前血脂谱、血糖、胰岛素、瘦素和脂联素水平以及血压。通过校正年龄和性别后的体重指数(BMI)标准差评分(SDS)变化评估治疗结果。

结果

我们招募了 144 名平均年龄为 14.3 ± 2.2 岁、平均 BMI 为 36.7 ± 6.2 kg/m²(对应 2.7 ± 0.4 BMI SDS)的儿童。在治疗期间辍学的 57 名患者和在康复期辍学的 44 名患者的治疗前 BMI 高于完成治疗的患者(平均 BMI,38.3 ± 6.8 kg/m²比 35.7 ± 5.5 kg/m²)和完成康复期的患者(平均 BMI,34.6 ± 5.3 kg/m²比 37.7 ± 6.3 kg/m²)(均 p<0.05)。此外,康复期参与者的年龄小于未参与者(平均年龄,13.4 ± 2.3 岁比 14.9 ± 2.0 岁,p<0.05)。患者在治疗期间平均体重减轻 1.0 ± 0.4 SDS,治疗后体重增加 0.4 ± 0.3 SDS,相当于体重增加 43 ± 27%(计算为治疗后 BMI SDS 增加量超过治疗期间 BMI SDS 减少量)。线性回归显示,更高的 BMI 和更多的合并症与 BMI SDS 降低呈负相关(均 p<0.05)。治疗后 BMI SDS 恢复的预测因素为治疗前的年龄、瘦素和脂联素水平。

结论

最需要治疗的患者辍学和体重反弹的风险增加,强调迫切需要干预措施来减少辍学并支持住院患者出院后的康复。此外,本研究首次报道治疗前瘦素和脂联素水平可预测治疗后 BMI SDS 的恢复,需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa39/9234213/e7c61564a1e8/fendo-13-822962-g001.jpg

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