{"title":"冷冻血清中神经丝轻链基质的比较及长期稳定性。","authors":"Lea Tybirk, Cindy Søndersø Knudsen, Tina Parkner","doi":"10.1016/j.cca.2025.120637","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Neurofilament light chain (NfL) is a sensitive biomarker of neuronal damage and degeneration increasingly used both in research and clinical practice. We aimed to investigate the relationship between NfL concentration in cerebrospinal fluid (CSF), serum, and lithium-heparin plasma samples, and the storage stability of NfL in serum at -20 °C.</p><p><strong>Methods: </strong>Serum and lithium-heparin plasma were compared by adding an extra lithium-heparin tube to routine serum NfL requisitions in our hospital until 50 samples were collected. Serum and CSF NfL were compared by extracting results of 955 paired samples from Danish hospitals taken within four hours of each other and analysed in our hospital laboratory. The stability of serum NfL during storage at -20 °C was assessed in 10 samples from the department of neurology, with repeated measurements performed over 12 months.</p><p><strong>Results: </strong>Very strong correlations were observed between serum and lithium-heparin plasma (Spearman's rho = 0.98) and between serum and CSF (Spearman's rho = 0.80). A small positive bias of 3.7 % was found for lithium-heparin plasma versus serum, while the median CSF/serum ratio was 54.5 (range: 1.6-385.6). In both comparisons, considerable variability across individual sample pairs was observed, independent of NfL concentration. In the stability study, the mean change from baseline was -7.1 % (95 %CI: -1.7 %; -12.6 %) after 12 months at -20 °C.</p><p><strong>Conclusions: </strong>NfL concentrations in different matrices were highly correlated, but due to variability across pairs, we recommend using the same matrix to monitor individual patients. Serum NfL concentrations remained stable during 12 months at -20 °C.</p>","PeriodicalId":10205,"journal":{"name":"Clinica Chimica Acta","volume":" ","pages":"120637"},"PeriodicalIF":2.9000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Neurofilament light chain - matrix comparison and long-term stability in frozen serum.\",\"authors\":\"Lea Tybirk, Cindy Søndersø Knudsen, Tina Parkner\",\"doi\":\"10.1016/j.cca.2025.120637\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Neurofilament light chain (NfL) is a sensitive biomarker of neuronal damage and degeneration increasingly used both in research and clinical practice. We aimed to investigate the relationship between NfL concentration in cerebrospinal fluid (CSF), serum, and lithium-heparin plasma samples, and the storage stability of NfL in serum at -20 °C.</p><p><strong>Methods: </strong>Serum and lithium-heparin plasma were compared by adding an extra lithium-heparin tube to routine serum NfL requisitions in our hospital until 50 samples were collected. Serum and CSF NfL were compared by extracting results of 955 paired samples from Danish hospitals taken within four hours of each other and analysed in our hospital laboratory. The stability of serum NfL during storage at -20 °C was assessed in 10 samples from the department of neurology, with repeated measurements performed over 12 months.</p><p><strong>Results: </strong>Very strong correlations were observed between serum and lithium-heparin plasma (Spearman's rho = 0.98) and between serum and CSF (Spearman's rho = 0.80). A small positive bias of 3.7 % was found for lithium-heparin plasma versus serum, while the median CSF/serum ratio was 54.5 (range: 1.6-385.6). In both comparisons, considerable variability across individual sample pairs was observed, independent of NfL concentration. In the stability study, the mean change from baseline was -7.1 % (95 %CI: -1.7 %; -12.6 %) after 12 months at -20 °C.</p><p><strong>Conclusions: </strong>NfL concentrations in different matrices were highly correlated, but due to variability across pairs, we recommend using the same matrix to monitor individual patients. Serum NfL concentrations remained stable during 12 months at -20 °C.</p>\",\"PeriodicalId\":10205,\"journal\":{\"name\":\"Clinica Chimica Acta\",\"volume\":\" \",\"pages\":\"120637\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinica Chimica Acta\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.cca.2025.120637\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MEDICAL LABORATORY TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinica Chimica Acta","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.cca.2025.120637","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
Neurofilament light chain - matrix comparison and long-term stability in frozen serum.
Objective: Neurofilament light chain (NfL) is a sensitive biomarker of neuronal damage and degeneration increasingly used both in research and clinical practice. We aimed to investigate the relationship between NfL concentration in cerebrospinal fluid (CSF), serum, and lithium-heparin plasma samples, and the storage stability of NfL in serum at -20 °C.
Methods: Serum and lithium-heparin plasma were compared by adding an extra lithium-heparin tube to routine serum NfL requisitions in our hospital until 50 samples were collected. Serum and CSF NfL were compared by extracting results of 955 paired samples from Danish hospitals taken within four hours of each other and analysed in our hospital laboratory. The stability of serum NfL during storage at -20 °C was assessed in 10 samples from the department of neurology, with repeated measurements performed over 12 months.
Results: Very strong correlations were observed between serum and lithium-heparin plasma (Spearman's rho = 0.98) and between serum and CSF (Spearman's rho = 0.80). A small positive bias of 3.7 % was found for lithium-heparin plasma versus serum, while the median CSF/serum ratio was 54.5 (range: 1.6-385.6). In both comparisons, considerable variability across individual sample pairs was observed, independent of NfL concentration. In the stability study, the mean change from baseline was -7.1 % (95 %CI: -1.7 %; -12.6 %) after 12 months at -20 °C.
Conclusions: NfL concentrations in different matrices were highly correlated, but due to variability across pairs, we recommend using the same matrix to monitor individual patients. Serum NfL concentrations remained stable during 12 months at -20 °C.
期刊介绍:
The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC)
Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells.
The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.