{"title":"Heart rate variability analysis of electrocardiography in pediatric immune-mediated autonomic neuropathy","authors":"Masafumi Sanefuji , Toshiyuki Maeda , Takashi Kumamoto , Yoshiyasu Ogata , Fumio Ichinose , Takuji Nakamura , Hiroto Doi , Shunya Nakane , Muneaki Matsuo","doi":"10.1016/j.nerep.2023.100187","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>Immune-mediated autonomic neuropathies are difficult to diagnose in childhood because of the extreme rarity, nonspecific symptoms, and infrequent detection of autoantibodies specific to the disorders. There is a need for objective testing methods that are easily applicable to pediatric patients.</p></div><div><h3>Description of case series</h3><p>Case 1 was a 13-year-old boy who showed autonomic symptoms of fatigue, tachycardia, and hypertension with sensorimotor impairments, including diminished tendon reflexes, delayed nerve conduction, and enhanced peripheral nerves on MRI. Case 2 was a 9-year-old boy who exhibited autonomic signs of postural orthostatic tachycardia with no abnormalities in a nerve conduction test and MRI but decreased heart rate variability (HRV) on conventional electrocardiography (ECG). Case 3 was a 14-year-old girl with autonomic symptoms of hypohidrosis, constipation, and coughing episodes, with alteration of various HRV metrics on 24-hour Holter ECG. Although serum autoantibodies to ganglionic acetylcholine receptor were not detected in any patients, intravenous immunoglobulin therapy was effective in all cases, suggesting immune-mediated mechanisms.</p></div><div><h3>Conclusion</h3><p>In the latter two patients, the diagnosis of immune-mediated autonomic neuropathies was underscored by HRV on ECG, especially 24-hour Holter ECG. Further studies are required to establish its clinical significance.</p></div>","PeriodicalId":100950,"journal":{"name":"Neuroimmunology Reports","volume":"4 ","pages":"Article 100187"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuroimmunology Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667257X23000256","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract
Introduction
Immune-mediated autonomic neuropathies are difficult to diagnose in childhood because of the extreme rarity, nonspecific symptoms, and infrequent detection of autoantibodies specific to the disorders. There is a need for objective testing methods that are easily applicable to pediatric patients.
Description of case series
Case 1 was a 13-year-old boy who showed autonomic symptoms of fatigue, tachycardia, and hypertension with sensorimotor impairments, including diminished tendon reflexes, delayed nerve conduction, and enhanced peripheral nerves on MRI. Case 2 was a 9-year-old boy who exhibited autonomic signs of postural orthostatic tachycardia with no abnormalities in a nerve conduction test and MRI but decreased heart rate variability (HRV) on conventional electrocardiography (ECG). Case 3 was a 14-year-old girl with autonomic symptoms of hypohidrosis, constipation, and coughing episodes, with alteration of various HRV metrics on 24-hour Holter ECG. Although serum autoantibodies to ganglionic acetylcholine receptor were not detected in any patients, intravenous immunoglobulin therapy was effective in all cases, suggesting immune-mediated mechanisms.
Conclusion
In the latter two patients, the diagnosis of immune-mediated autonomic neuropathies was underscored by HRV on ECG, especially 24-hour Holter ECG. Further studies are required to establish its clinical significance.