{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,27]],"date-time":"2026-02-27T19:13:41Z","timestamp":1772219621185,"version":"3.50.1"},"reference-count":65,"publisher":"Public Library of Science (PLoS)","issue":"10","license":[{"start":{"date-parts":[[2024,10,28]],"date-time":"2024-10-28T00:00:00Z","timestamp":1730073600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"Takeda Development Center Americas Inc."},{"name":"Takeda Development Center Americas Inc."},{"name":"Takeda Development Center Americas Inc."},{"name":"Takeda Development Center Americas Inc."}],"content-domain":{"domain":["www.plosone.org"],"crossmark-restriction":false},"short-container-title":["PLoS ONE"],"abstract":"<jats:p>\n                    Fabry disease, an X-linked lysosomal storage disorder caused by galactosidase \u03b1 (GLA) gene mutations, exhibits diverse clinical manifestations, and poses significant diagnostic challenges. Early diagnosis and treatment are crucial for improved patient outcomes, pressing the need for reliable biomarkers. In this study, we aimed to identify miRNA candidates as potential biomarkers for Fabry disease using the KingFisher\u2122 automated isolation method and NanoString nCounter\u00ae miRNA detection assay. Clinical serum samples were collected from both healthy subjects and Fabry disease patients. RNA extraction from the samples was performed using the KingFisher\u2122 automated isolation method with the MagMAX mirVana\n                    <jats:sup>TM<\/jats:sup>\n                    kit or manually using the Qiagen miRNeasy kit. The subsequent NanoString nCounter\u00ae miRNA detection assay showed consistent performance and no correlation between RNA input concentration and raw count, ensuring reliable and reproducible results. Interestingly, the detection range and highly differential miRNA between the control and disease groups were found to be distinct depending on the isolation method employed. Nevertheless, enrichment analysis of miRNA-targeting genes consistently revealed significant associations with angiogenesis pathways in both isolation methods. Additionally, our investigation into the impact of enzyme replacement therapy on miRNA expression indicated that some differential miRNAs may be sensitive to treatment. Our study provides valuable insights to identify miRNA biomarkers for Fabry disease. While different isolation methods yielded various detection ranges and highly differential miRNAs, the consistent association with angiogenesis pathways suggests their significance in disease progression. These findings lay the groundwork for further investigations and validation studies, ultimately leading to the development of non-invasive and reliable biomarkers to aid in early diagnosis and treatment monitoring for Fabry disease.\n                  <\/jats:p>","DOI":"10.1371\/journal.pone.0301733","type":"journal-article","created":{"date-parts":[[2024,10,28]],"date-time":"2024-10-28T13:32:27Z","timestamp":1730122347000},"page":"e0301733","update-policy":"https:\/\/doi.org\/10.1371\/journal.pone.corrections_policy","source":"Crossref","is-referenced-by-count":0,"title":["Exploring the diagnostic potential of miRNA signatures in the Fabry disease serum: A comparative study of automated and manual sample isolations"],"prefix":"10.1371","volume":"19","author":[{"ORCID":"https:\/\/orcid.org\/0009-0004-9129-7520","authenticated-orcid":true,"given":"Josephine Y.","family":"Fang","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0009-0009-3296-705X","authenticated-orcid":true,"given":"Saravanan","family":"Ayyadurai","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alyssa F.","family":"Pybus","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hiroshi","family":"Sugimoto","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mark G.","family":"Qian","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"340","published-online":{"date-parts":[[2024,10,28]]},"reference":[{"issue":"1","key":"pone.0301733.ref001","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1186\/1750-1172-5-30","article-title":"Fabry disease.","volume":"5","author":"DP Germain","year":"2010","journal-title":"Orphanet journal of rare diseases"},{"key":"pone.0301733.ref002","doi-asserted-by":"crossref","first-page":"s10","DOI":"10.1590\/1806-9282.66.s1.10","article-title":"Fabry disease: genetics, pathology, and treatment.","volume":"66","author":"TP Bernardes","year":"2020","journal-title":"Revista da Associa\u00e7\u00e3o M\u00e9dica Brasileira."},{"key":"pone.0301733.ref003","article-title":"Demographics of FOS\u2013the Fabry outcome survey","author":"M. 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