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The role of peroxisome proliferator-activated receptor gamma and adiponectin in children with Kawasaki disease.过氧化物酶体增殖物激活受体γ和脂联素在川崎病患儿中的作用。
J Int Med Res. 2021 Mar;49(3):300060521994925. doi: 10.1177/0300060521994925.
2
Macrophage activation syndrome in children with Kawasaki disease: an experience from a tertiary care hospital in northwest India.儿童川崎病中的巨噬细胞活化综合征:来自印度西北部一家三级护理医院的经验。
Rheumatology (Oxford). 2021 Jul 1;60(7):3413-3419. doi: 10.1093/rheumatology/keaa715.
3
Kawasaki Disease in Children Older Than 10 Years: A Clinical Experience From Northwest India.10岁以上儿童的川崎病:来自印度西北部的临床经验
Front Pediatr. 2020 Feb 14;8:24. doi: 10.3389/fped.2020.00024. eCollection 2020.
4
Association of circulating resistin and adiponectin levels with Kawasaki disease: A meta-analysis.循环抵抗素和脂联素水平与川崎病的关联:一项荟萃分析。
Exp Ther Med. 2020 Feb;19(2):1033-1041. doi: 10.3892/etm.2019.8306. Epub 2019 Dec 9.
5
Adiponectin Expression Is Modulated by Long-Term Physical Activity in Adult Patients Affected by Cystic Fibrosis.脂联素表达受成年囊性纤维化患者长期体力活动的调节。
Mediators Inflamm. 2019 Sep 9;2019:2153934. doi: 10.1155/2019/2153934. eCollection 2019.
6
Circulating adipokines are associated with Kawasaki disease.循环脂肪因子与川崎病相关。
Pediatr Rheumatol Online J. 2018 May 8;16(1):33. doi: 10.1186/s12969-018-0243-z.
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Supervised physical exercise improves clinical, anthropometric and biochemical parameters in adult cystic fibrosis patients: A 2-year evaluation.监督下的体育锻炼可改善成年囊性纤维化患者的临床、人体测量和生化参数:一项为期两年的评估。
Clin Respir J. 2018 Jul;12(7):2228-2234. doi: 10.1111/crj.12796. Epub 2018 Apr 30.
8
Carotid Intima-Media Thickness and Lipid Profile in Children With Kawasaki Disease: A Single-Center Follow-up Study After a Mean Duration of 6.9 Years.川崎病患儿颈动脉内中膜厚度及血脂谱:平均 6.9 年后的单中心随访研究。
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Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Scientific Statement for Health Professionals From the American Heart Association.川崎病的诊断、治疗和长期管理:美国心脏协会发布的一份面向医疗保健专业人员的科学声明。
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10
Inflammation, metabolism and adipokines: toward a unified theory.炎症、代谢与脂肪因子:迈向统一理论
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平均随访5.5年的川崎病患儿脂肪细胞因子谱:一项来自印度北部的研究。

Adipocytokine profile in children with Kawasaki disease at a mean follow-up period of 5.5 years: A study from North India.

作者信息

Praharaj Dibya Lochan, Rawat Amit, Gupta Anju, Arora Kanika, Pilania Rakesh Kumar, Bhattad Sagar, Singh Surjit

机构信息

Pediatric Allergy and Immunology Unit, Advanced Pediatrics Centre, Post Graduate Institute of Medical Education and Research, Chandigarh 160012, India.

出版信息

World J Clin Pediatr. 2022 Jul 9;11(4):360-368. doi: 10.5409/wjcp.v11.i4.360.

DOI:10.5409/wjcp.v11.i4.360
PMID:36052116
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9331403/
Abstract

BACKGROUND

Kawasaki disease (KD) is an acute self-limited vasculitis with a predilection for coronary arteries. Children with KD may have altered lipid metabolism and abnormal lipid profiles that may last for prolonged periods. However, there is a paucity of literature on the role of adipocytokines in KD.

AIM

To estimate the levels of adipocytokines (adiponectin, leptin and resistin) during the convalescent phase of KD.

METHODS

Twenty children, who had KD at least three years earlier, were enrolled in this study. In addition, 20 healthy controls were also enrolled. Clinical and laboratory profiles of patients were obtained from hospital records. Serum adiponectin, leptin and resistin levels were estimated by enzyme-linked immunosorbent assay.

RESULTS

Mean age of the patients in the study group was 10.15 ± 3 years and the male: female ratio was 1.5:1. Median serum resistin levels in patients with KD (27.77 ng/mL; [IQR: 18.66, 48.90]) were decreased compared to controls (21.20 ng/mL; [IQR: 14.80, 27.00]) ( = 0.04). Median serum leptin levels in cases and controls were 1.83 ng/mL; (IQR: 1.13, 3.80), and 1.10 ng/mL; (IQR: 0.41, 2.88), respectively ( = 0.09). Median serum adiponectin levels were similar in both cases (12.20 µg/mL; [IQR: 9.76, 17.97]) and controls (13.95 µg/mL; [IQR: 11.17, 22.58]); ( = 0.18). There was no significant difference in all 3 adipocytokines between children with (4/20) and without coronary artery abnormalities (16/20).

CONCLUSION

Serum resistin levels were significantly elevated in patients with KD during the convalescent phase compared to controls. Serum leptin levels appeared to be higher in patients with KD, although the difference was not statistically significant. Adiponectin levels were similar in both cases and controls. Raised resistin and leptin levels may partially explain lipid perturbations observed during the convalescent phase of KD.

摘要

背景

川崎病(KD)是一种急性自限性血管炎,易累及冠状动脉。患KD的儿童可能存在脂质代谢改变和血脂异常,且这种情况可能持续较长时间。然而,关于脂肪细胞因子在KD中的作用的文献较少。

目的

评估KD恢复期脂肪细胞因子(脂联素、瘦素和抵抗素)的水平。

方法

本研究纳入了至少在三年前患过KD的20名儿童。此外,还纳入了20名健康对照。患者的临床和实验室资料从医院记录中获取。采用酶联免疫吸附测定法评估血清脂联素、瘦素和抵抗素水平。

结果

研究组患者的平均年龄为10.15±3岁,男女比例为1.5:1。KD患者的血清抵抗素水平中位数(27.77 ng/mL;[四分位间距:18.66,48.90])低于对照组(21.20 ng/mL;[四分位间距:14.80,27.00])(P = 0.04)。病例组和对照组的血清瘦素水平中位数分别为1.83 ng/mL;(四分位间距:1.13,3.80)和1.10 ng/mL;(四分位间距:0.41,2.88)(P = 0.09)。病例组(12.20 µg/mL;[四分位间距:9.76,17.97])和对照组(13.95 µg/mL;[四分位间距:11.17,22.58])的血清脂联素水平中位数相似;(P = 0.18)。有冠状动脉异常(4/20)和无冠状动脉异常(16/20)的儿童在所有3种脂肪细胞因子方面均无显著差异。

结论

与对照组相比,KD患者在恢复期血清抵抗素水平显著升高。KD患者的血清瘦素水平似乎较高,尽管差异无统计学意义。病例组和对照组的脂联素水平相似。抵抗素和瘦素水平升高可能部分解释了KD恢复期观察到的脂质紊乱。