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非肥胖阻塞性睡眠呼吸暂停综合征患儿的心脏代谢风险特征。

Cardiometabolic risk profile in non-obese children with obstructive sleep apnea syndrome.

机构信息

Department of Woman, Child, and General and Specialized Surgery, University of Campania "Luigi Vanvitelli", Naples, Italy.

Department of Clinical and Experimental Medicine, University of Foggia, Foggia, Italy.

出版信息

Eur J Pediatr. 2022 Apr;181(4):1689-1697. doi: 10.1007/s00431-021-04366-8. Epub 2022 Jan 10.

Abstract

UNLABELLED

Obstructive sleep apnea syndrome (OSAS) in childhood is a complex disease primarily due both to adenotonsillar hypertrophy and pediatric obesity. Notably, inflammation has been recognized as one of the most important shared pathogenic factor between obesity and OSAS resulting in an increased cardiometabolic risk for these patients. To date, evidence is still limited in non-obese population with OSAS. We aimed to evaluate the cardiometabolic risk profile of a pediatric population of non-obese subjects affected by OSAS. A total of 128 school-aged children (mean age 9.70 ± 3.43) diagnosed with OSAS and 213 non-OSAS children (mean age 9.52 ± 3.35) as control group were enrolled. All subjects underwent a complete clinical and biochemical assessment (including white blood cell count (WBC), platelet count (PLT), mean platelet volume (MPV), % of neutrophils (NEU%), C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), serum glucose, aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma-glutamyl transpeptidase (GGT), uric acid, fasting insulin, iron, ferritin, and transferrin levels). A significant association between inflammation markers (including WBC, PLT, MPV, NEU%, ferritin, CPR, and ESR) and OSAS was found (all p < 0.001). Children with OSAS also showed increased transaminase, glucose, uric acid, and insulin levels (all p < 0.001) compared to healthy controls.

CONCLUSION

Taken together, these findings suggested a worse cardiometabolic profile in non-obese children with OSAS. Given the pivotal pathogenic role of inflammation both for hypoxiemia and metabolic derangements, therapeutic strategies for OSAS might also counteract the increased cardiometabolic risk of these patients, by improving their long-term quality of life.

WHAT IS KNOWN

• Pediatric OSAS has shown a close relationship with obesity and its cardiometabolic comorbidities. • Inflammation represents the hallmark of both obesity and OSAS.

WHAT IS NEW

• Non obese children with OSAS presented with a worse cardiometabolic risk profile. • OSAS treatment might serve as an effective approach also for the increased cardiometabolic risk of these children.

摘要

目的

评估非肥胖阻塞性睡眠呼吸暂停综合征(OSAS)患儿的心脏代谢风险特征。

方法

共纳入 128 名学龄期 OSAS 患儿(平均年龄 9.70 ± 3.43 岁)和 213 名非 OSAS 患儿(平均年龄 9.52 ± 3.35 岁)作为对照组。所有受试者均接受了完整的临床和生化评估(包括白细胞计数、血小板计数、平均血小板体积、中性粒细胞百分比、C 反应蛋白、红细胞沉降率、血糖、天门冬氨酸氨基转移酶、丙氨酸氨基转移酶、γ-谷氨酰转肽酶、尿酸、空腹胰岛素、铁、铁蛋白和转铁蛋白水平)。

结果

OSAS 患儿的炎症标志物(包括白细胞计数、血小板计数、平均血小板体积、中性粒细胞百分比、铁蛋白、C 反应蛋白和红细胞沉降率)与 OSAS 显著相关(均 p<0.001)。与健康对照组相比,OSAS 患儿的转氨酶、血糖、尿酸和胰岛素水平也显著升高(均 p<0.001)。

结论

非肥胖 OSAS 患儿的心脏代谢特征更差。鉴于炎症在低氧血症和代谢紊乱中起着关键的致病作用,OSAS 的治疗策略可能通过改善患者的长期生活质量,从而抵消这些患者的心脏代谢风险增加。

已知

肥胖与 OSAS 及其心脏代谢合并症密切相关。炎症是肥胖和 OSAS 的共同特征。

新发现

非肥胖 OSAS 患儿的心脏代谢风险更高。OSAS 的治疗可能是一种有效的方法,也可以降低这些儿童的心脏代谢风险。

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