D. Eratne, M. Kang, C. Lewis, C. Dang, C. Malpas, M. Keem, J. Grewal, Vladimir Marinov, A. Coe, Cath Kaylor-Hughes, Thomas Borchard, Chhoa Keng-Hong, Alexandra Waxmann, Burcu Saglam, Tomáš Kalinčík, Richard Kanaan, W. Kelso, Andrew Evans, S. Farrand, S. Loi, M. Walterfang, C. Stehmann, Qiao-Xin Li, Steven Collins, C. L. Masters, A. Santillo, Henrik Zetterberg, K. Blennow, S. Berkovic, Dennis Velakoulis, Terence J. O’Brien, Patrick Kwan, O. Hansson, Christopher Fowler, Jane Gunn
{"title":"血浆和脑脊液神经丝蛋白轻链在临床中区分神经退行性疾病和原发性精神疾病","authors":"D. Eratne, M. Kang, C. Lewis, C. Dang, C. Malpas, M. Keem, J. Grewal, Vladimir Marinov, A. Coe, Cath Kaylor-Hughes, Thomas Borchard, Chhoa Keng-Hong, Alexandra Waxmann, Burcu Saglam, Tomáš Kalinčík, Richard Kanaan, W. Kelso, Andrew Evans, S. Farrand, S. Loi, M. Walterfang, C. Stehmann, Qiao-Xin Li, Steven Collins, C. L. Masters, A. Santillo, Henrik Zetterberg, K. Blennow, S. Berkovic, Dennis Velakoulis, Terence J. O’Brien, Patrick Kwan, O. Hansson, Christopher Fowler, Jane Gunn","doi":"10.1101/2024.08.11.24311847","DOIUrl":null,"url":null,"abstract":"INTRODUCTION: Many patients with neurodegenerative disorders (ND) face diagnostic delay and misdiagnosis. We investigated blood and cerebrospinal fluid (CSF) neurofilament light chain (NfL) to distinguish ND from primary psychiatric disorders (ND), a common challenge in clinical settings. METHODS: Plasma and CSF NfL levels were measured and compared between groups, adjusting for age, sex, weight. RESULTS: 337 participants included: 136 ND, 77 PPD, 124 Controls. Plasma NfL was 2.5 fold elevated in ND compared to PPD and had strong diagnostic performance (area under the curve, AUC 0.86, 81%/85% specificity/sensitivity) that was comparable to CSF NfL (2 fold elevated, AUC 0.89, 95%/71% specificity/sensitivity). Diagnostic performance was especially strong in younger people (40-<60years). Additional findings were cut-offs optimised for sensitivity and specificity, and issues important for future clinical translation CONCLUSIONS: This study adds important evidence for a simple blood-based biomarker to assist as a screening test for neurodegeneration and distinction from PPD, in clinical settings.","PeriodicalId":18505,"journal":{"name":"medRxiv","volume":"11 41","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Plasma and CSF neurofilament light chain distinguish neurodegenerative from primary psychiatric conditions in a clinical setting\",\"authors\":\"D. Eratne, M. Kang, C. Lewis, C. Dang, C. Malpas, M. Keem, J. Grewal, Vladimir Marinov, A. Coe, Cath Kaylor-Hughes, Thomas Borchard, Chhoa Keng-Hong, Alexandra Waxmann, Burcu Saglam, Tomáš Kalinčík, Richard Kanaan, W. Kelso, Andrew Evans, S. Farrand, S. Loi, M. Walterfang, C. Stehmann, Qiao-Xin Li, Steven Collins, C. L. Masters, A. Santillo, Henrik Zetterberg, K. Blennow, S. Berkovic, Dennis Velakoulis, Terence J. O’Brien, Patrick Kwan, O. Hansson, Christopher Fowler, Jane Gunn\",\"doi\":\"10.1101/2024.08.11.24311847\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"INTRODUCTION: Many patients with neurodegenerative disorders (ND) face diagnostic delay and misdiagnosis. We investigated blood and cerebrospinal fluid (CSF) neurofilament light chain (NfL) to distinguish ND from primary psychiatric disorders (ND), a common challenge in clinical settings. METHODS: Plasma and CSF NfL levels were measured and compared between groups, adjusting for age, sex, weight. RESULTS: 337 participants included: 136 ND, 77 PPD, 124 Controls. Plasma NfL was 2.5 fold elevated in ND compared to PPD and had strong diagnostic performance (area under the curve, AUC 0.86, 81%/85% specificity/sensitivity) that was comparable to CSF NfL (2 fold elevated, AUC 0.89, 95%/71% specificity/sensitivity). Diagnostic performance was especially strong in younger people (40-<60years). Additional findings were cut-offs optimised for sensitivity and specificity, and issues important for future clinical translation CONCLUSIONS: This study adds important evidence for a simple blood-based biomarker to assist as a screening test for neurodegeneration and distinction from PPD, in clinical settings.\",\"PeriodicalId\":18505,\"journal\":{\"name\":\"medRxiv\",\"volume\":\"11 41\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-08-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"medRxiv\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/2024.08.11.24311847\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"medRxiv","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.08.11.24311847","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Plasma and CSF neurofilament light chain distinguish neurodegenerative from primary psychiatric conditions in a clinical setting
INTRODUCTION: Many patients with neurodegenerative disorders (ND) face diagnostic delay and misdiagnosis. We investigated blood and cerebrospinal fluid (CSF) neurofilament light chain (NfL) to distinguish ND from primary psychiatric disorders (ND), a common challenge in clinical settings. METHODS: Plasma and CSF NfL levels were measured and compared between groups, adjusting for age, sex, weight. RESULTS: 337 participants included: 136 ND, 77 PPD, 124 Controls. Plasma NfL was 2.5 fold elevated in ND compared to PPD and had strong diagnostic performance (area under the curve, AUC 0.86, 81%/85% specificity/sensitivity) that was comparable to CSF NfL (2 fold elevated, AUC 0.89, 95%/71% specificity/sensitivity). Diagnostic performance was especially strong in younger people (40-<60years). Additional findings were cut-offs optimised for sensitivity and specificity, and issues important for future clinical translation CONCLUSIONS: This study adds important evidence for a simple blood-based biomarker to assist as a screening test for neurodegeneration and distinction from PPD, in clinical settings.