Zhu Guoliang, Yan Guifang, Luo Ying, Luo Juan
School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Department of Hepatopancreatobiliary Surgery, The First Affiliated Hospital of Chengdu Medical College, Chengdu, China.
Eur J Pain. 2026 Jan;30(1):e70177. doi: 10.1002/ejp.70177.
Although calcitonin gene-related peptide (CGRP) has emerged as a promising therapeutic target in migraine management, current clinical evidence regarding its dynamic variations in paediatric migraine populations remains inconclusive. We conducted a meta-analysis to explore the relationship between blood CGRP levels and paediatric migraine.
We systematically searched for observational studies that reported CGRP levels in paediatric migraine published in English from the PubMed, Web of Science, and Embase electronic databases, or in Chinese from the Chinese National Knowledge Infrastructure and the WanFang Med database. The Newcastle-Ottawa Quality Assessment Scale was used to assess the quality of the included studies. The quality of evidence for each outcome was assessed according to the Grading of Recommendations, Assessment, Development, and Evaluation guidelines.
Of the 1134 identified studies, eight were eligible for inclusion. There was a 'Moderate' level of evidence demonstrating significantly elevated CGRP levels in children with migraine compared to controls (standardised mean difference [SMD] = 1.44, 95% CI 0.61-2.31). Stratification analysis showed the 'Low' level of evidence revealed higher levels during both ictal (SMD = 2.39, 95% CI 0.59-4.19) and interictal phases (SMD = 1.27, 95% CI 0.54-1.99). 'Very low' quality of evidence supported paediatric migraine patients with (SMD = 1.47, 95% CI 0.67-2.27) and without (SMD = 1.11, 95% CI 0.50-1.72) aura had higher CGRP levels than non-migraine controls.
Our findings suggest that CGRP levels may be a potential diagnostic biomarker and prophylactic therapeutic target for paediatric migraine, but need high-quality longitudinal studies to validate.
This systematic review and meta-analysis provides significant evidence that CGRP levels serve as a potential diagnostic biomarker for migraine in children and adolescents. Future research should further explore the diagnostic value of CGRP levels in this population. However, the current evidence does not confirm CGRP as an acute-phase therapeutic target for pediatric and adolescent migraine, necessitating validation through higher-quality studies.
PROSPERO number: CRD42025635332.
尽管降钙素基因相关肽(CGRP)已成为偏头痛治疗中一个有前景的治疗靶点,但目前关于其在儿童偏头痛人群中动态变化的临床证据仍不明确。我们进行了一项荟萃分析,以探讨血CGRP水平与儿童偏头痛之间的关系。
我们系统检索了在PubMed、Web of Science和Embase电子数据库中以英文发表的、或在中国国家知识基础设施和万方医学数据库中以中文发表的、报道儿童偏头痛患者CGRP水平的观察性研究。采用纽卡斯尔-渥太华质量评估量表评估纳入研究的质量。根据推荐分级、评估、制定和评价指南评估每个结局的证据质量。
在1134项确定的研究中,8项符合纳入标准。有“中等”水平的证据表明,与对照组相比,偏头痛儿童的CGRP水平显著升高(标准化均数差[SMD]=1.44,95%CI 0.61-2.31)。分层分析显示,“低”水平的证据表明,在发作期(SMD=2.39,95%CI 0.59-4.19)和发作间期(SMD=1.27,95%CI 0.54-1.99)CGRP水平均较高。“极低”质量的证据支持有先兆(SMD=1.47,95%CI 0.67-2.27)和无先兆(SMD=1.11,95%CI 0.50-1.72)的儿童偏头痛患者的CGRP水平高于非偏头痛对照组。
我们的研究结果表明,CGRP水平可能是儿童偏头痛的潜在诊断生物标志物和预防性治疗靶点,但需要高质量的纵向研究来验证。
这项系统评价和荟萃分析提供了重要证据,表明CGRP水平可作为儿童和青少年偏头痛的潜在诊断生物标志物。未来的研究应进一步探索CGRP水平在该人群中的诊断价值。然而,目前的证据并未证实CGRP是儿童和青少年偏头痛的急性期治疗靶点,需要通过更高质量的研究来验证。
国际前瞻性系统评价注册库编号:CRD42025635332。