Inflammatory Markers in Children and Adolescents with Functional Somatic Disorders: A Systematic Review

被引:1
作者
Hansen, Anne Sofie [1 ,2 ]
Rask, Charlotte Ulrikka [3 ,4 ]
Kallesoe, Karen Hansen [3 ,4 ]
机构
[1] Aalborg Univ Hosp, Dept Child & Adolescent Psychiat, DK-9000 Aalborg, Denmark
[2] Aalborg Univ, Dept Clin Med, DK-9000 Aalborg, Denmark
[3] Aarhus Univ Hosp Psychiat, Dept Child & Adolescent Psychiat, DK-8200 Aarhus N, Denmark
[4] Aarhus Univ, Dept Clin Med, DK-8200 Aarhus N, Denmark
来源
CHILDREN-BASEL | 2024年 / 11卷 / 05期
关键词
functional somatic disorders; low-grade inflammation; cytokines; children; adolescents; CHRONIC-FATIGUE-SYNDROME; SYMPTOMS; CYTOKINES; MECHANISMS; QUALITY;
D O I
10.3390/children11050549
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Functional somatic disorders (FSDs) are common in children and adolescents. Recent findings suggest that low-grade inflammation has a role in the development and maintenance of pediatric FSDs. This systematic review included studies with original data on systemic inflammatory markers in children and adolescents with an FSD compared to individuals without an FSD. The literature search identified 1374 articles. After assessment, a total of 15 studies met the inclusion criteria. In total, 41 serum or plasma cytokines were assayed in a population of 696 children and adolescents. Altered cytokine levels in patients with FSDs were reported in 12 studies, whereas three studies found no significant differences when comparing patients with FSDs and controls. The cytokine levels were significantly elevated in nine studies (i.e., IL-2, IL-6, IL-8, IL-12 (p70), CRP, hsCRP, IP-10, MCP-1, sTIM-3, sCD25 and TNF-alpha). The findings indicate that inflammatory response may have a role in the pathophysiology of pediatric FSDs. However, the included studies showed limited quality with potential risk of bias, small study populations and a narrow spectrum of included FSDs, which limits the generalizability of the results. To further explore the potential link between inflammatory markers and pediatric FSDs, future research using a longitudinal study design is recommended.
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页数:12
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