CGRP and PACAP-38 play an important role in diagnosing pediatric migraine

被引:19
作者
Liu, Junhui [1 ]
Wang, Guan [1 ]
Dan, Yuan [1 ]
Liu, Xinjie [1 ]
机构
[1] Shandong Univ, Dept Pediat, Qilu Hosp, 107 West Wenhua Rd, Jinan 250012, Shandong, Peoples R China
关键词
Pediatric migraine; Pituitary adenylate cyclase-activating polypeptide-38; Calcitonin gene-related peptide; ROC curve; Logistic regression; Diagnostic value; GENE-RELATED PEPTIDE; CORTICAL SPREADING DEPRESSION; PRIMARY HEADACHES; PLASMA; CHILDREN; NEURONS; SENSITIZATION; POPULATION; PREVALENCE; INCREASE;
D O I
10.1186/s10194-022-01435-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: An increasing number of studies have suggested that the important role of vasoactive peptides, such as pituitary adenylate cyclase-activating polypeptide-38 (PACAP-38) and calcitonin gene-related peptide (CGRP), in the pathophysiology of migraine seems undeniable in adults, but studies in pediatric migraine patients remain scarce. We prospectively investigated CGRP and PACAP-38 plasma levels in children with migraine during ictal and interictal periods and compared the results between migraine patients with aura and without aura. We were the first to explore the diagnostic value of a combination of CGRP and PACAP-38. Methods: Seventy-six migraine patients aged 4-18 years and seventy-seven age-matched healthy children were included in the study. Plasma vasoactive peptides were measured using the enzyme-linked immunosorbent assay (ELISA). Differences and correlations of groups were analyzed using the independent samples t-test, analysis of variance (ANOVA), Mann-Whitney U test, and multiple linear regression. We also performed logistic regression and receiver operating characteristic curve (ROC) analyses to evaluate the diagnostic value of CGRP and PACAP-38 in pediatric migraine. Results: PACAP-38 and CGRP levels in migraine patients during the ictal and interictal periods were higher than those in controls (p < 0.001). PACAP-38 and CGRP levels in migraine patients with aura and without aura were higher than those in controls (p < 0.001). PACAP-38 and CGRP were independent risk factors in diagnosing pediatric migraine (adjusted OR (PACAP-38) =1.331, 95% CI: 1.177-1.506, p <0.001; adjusted OR (CGRP) = 1.113, 95% CI: 1.064-1.165, p<0.001). Area Under Curve (AUC) comparison: Combination (0.926) > CGRP (0.869) > PACAP-38 (0.867). Conclusions: Our study found almost the same changes in CGRP and PACAP levels in pediatric migraine, suggesting that CGRP and PACAP-38 may work together to play an integral role in pediatric migraine. Higher CGRP levels were found in the ictal phase than in the interictal phase and with aura group than without aura group, indicating that CGRP may take part in the formation of pain and aura. Moreover, ROC and logistic regression analyses suggested that CGRP and PACAP-38 are good indicators to diagnose pediatric migraine, and the combination of CGRP and PACAP-38 was valuable in diagnosing pediatric migraine and differentiating pediatric migraine from non-migraine headaches.
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页数:13
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