{"title":"戈谢病携带者的经颅超声检查。","authors":"Fatemeh Omrani, Shahla Ansari-Damavandi, Babak Zamani, Zahra Omrani, Nahid Mohammadzade, Sadra Rohani, Mohammad Rohani","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p><b>Background:</b> Glucocerebrosidase (GBA) mutation is the most common genetic risk factor in Parkinson's disease (PD). Transcranial sonography (TCS) shows increased substantia nigra (SN) echogenicity in both idiopathic and genetic forms of PD. The goal of this study was to compare maximal area of SN hyperechogenicity (aSNmax) and diameter of third ventricle (DTV) between GBA mutation carriers and healthy controls. <b>Methods:</b> Twenty-six carriers of GBA mutation and twenty-six healthy controls underwent TCS. The aSNmax and the DTV were measured. Mini-mental status examination (MMSE) and demographic data of the subjects were recorded, too. <b>Results:</b> Mean aSNmax in GBA mutation carriers was significantly higher (0.31 ± 0.06 cm<sup>2</sup>) than controls (0.16 ± 0.04 cm<sup>2</sup>). Moreover, DTV was significantly higher in GBA mutation carriers group (3.98 ± 0.90 vs 3.29 ± 0.56 cm). <b>Conclusion:</b> Increased SN echogenicity and increased third ventricle diameter in GBA mutation carriers may be caused by alterations in iron metabolism with reference to their genetic status.</p>","PeriodicalId":45759,"journal":{"name":"Iranian Journal of Neurology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2018-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420695/pdf/","citationCount":"0","resultStr":"{\"title\":\"Transcranial sonography in carriers of Gaucher disease.\",\"authors\":\"Fatemeh Omrani, Shahla Ansari-Damavandi, Babak Zamani, Zahra Omrani, Nahid Mohammadzade, Sadra Rohani, Mohammad Rohani\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Background:</b> Glucocerebrosidase (GBA) mutation is the most common genetic risk factor in Parkinson's disease (PD). Transcranial sonography (TCS) shows increased substantia nigra (SN) echogenicity in both idiopathic and genetic forms of PD. The goal of this study was to compare maximal area of SN hyperechogenicity (aSNmax) and diameter of third ventricle (DTV) between GBA mutation carriers and healthy controls. <b>Methods:</b> Twenty-six carriers of GBA mutation and twenty-six healthy controls underwent TCS. The aSNmax and the DTV were measured. Mini-mental status examination (MMSE) and demographic data of the subjects were recorded, too. <b>Results:</b> Mean aSNmax in GBA mutation carriers was significantly higher (0.31 ± 0.06 cm<sup>2</sup>) than controls (0.16 ± 0.04 cm<sup>2</sup>). Moreover, DTV was significantly higher in GBA mutation carriers group (3.98 ± 0.90 vs 3.29 ± 0.56 cm). <b>Conclusion:</b> Increased SN echogenicity and increased third ventricle diameter in GBA mutation carriers may be caused by alterations in iron metabolism with reference to their genetic status.</p>\",\"PeriodicalId\":45759,\"journal\":{\"name\":\"Iranian Journal of Neurology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-07-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420695/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Iranian Journal of Neurology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Iranian Journal of Neurology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景:糖脑苷酶(GBA)突变是帕金森病(PD)最常见的遗传危险因素。经颅超声(TCS)显示特发性和遗传性PD的黑质(SN)回声增强。本研究的目的是比较GBA突变携带者和健康对照组的最大SN高回声面积(aSNmax)和第三脑室直径(DTV)。方法:对26例GBA突变携带者和26例健康对照进行TCS。测量了aSNmax和DTV。同时记录受试者的简易精神状态检查(MMSE)和人口统计数据。结果:GBA突变携带者的平均aSNmax(0.31±0.06 cm2)显著高于对照组(0.16±0.04 cm2)。此外,GBA突变携带者组的DTV(3.98±0.90 cm vs 3.29±0.56 cm)显著高于前者。结论:GBA突变携带者SN回声增强、第三脑室直径增大可能与铁代谢改变有关,并与基因状况有关。
Transcranial sonography in carriers of Gaucher disease.
Background: Glucocerebrosidase (GBA) mutation is the most common genetic risk factor in Parkinson's disease (PD). Transcranial sonography (TCS) shows increased substantia nigra (SN) echogenicity in both idiopathic and genetic forms of PD. The goal of this study was to compare maximal area of SN hyperechogenicity (aSNmax) and diameter of third ventricle (DTV) between GBA mutation carriers and healthy controls. Methods: Twenty-six carriers of GBA mutation and twenty-six healthy controls underwent TCS. The aSNmax and the DTV were measured. Mini-mental status examination (MMSE) and demographic data of the subjects were recorded, too. Results: Mean aSNmax in GBA mutation carriers was significantly higher (0.31 ± 0.06 cm2) than controls (0.16 ± 0.04 cm2). Moreover, DTV was significantly higher in GBA mutation carriers group (3.98 ± 0.90 vs 3.29 ± 0.56 cm). Conclusion: Increased SN echogenicity and increased third ventricle diameter in GBA mutation carriers may be caused by alterations in iron metabolism with reference to their genetic status.