Detection of primary myelofibrosis in blood serum via Raman spectroscopy assisted by machine learning approaches; correlation with clinical diagnosis
Primary myelofibrosis (PM) is one of the myeloproliferative neoplasm, where stem cell-derived clonal neoplasms was noticed. Diagnosis of this disease is based on: physical examination, peripheral blood findings, bone marrow morphology, cytogenetics, and molecular markers. However, the molecular mark...
Gespeichert in:
Veröffentlicht in: | Nanomedicine 2023-09, Vol.53, p.102706-102706, Article 102706 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 102706 |
---|---|
container_issue | |
container_start_page | 102706 |
container_title | Nanomedicine |
container_volume | 53 |
creator | Guleken, Zozan Ceylan, Zeynep Aday, Aynur Bayrak, Ayşe Gül Hindilerden, İpek Yönal Nalçacı, Meliha Jakubczyk, Paweł Jakubczyk, Dorota Kula-Maximenko, Monika Depciuch, Joanna |
description | Primary myelofibrosis (PM) is one of the myeloproliferative neoplasm, where stem cell-derived clonal neoplasms was noticed. Diagnosis of this disease is based on: physical examination, peripheral blood findings, bone marrow morphology, cytogenetics, and molecular markers. However, the molecular marker of PM, which is a mutation in the JAK2V617F gene, was observed also in other myeloproliferative neoplasms such as polycythemia vera and essential thrombocythemia. Therefore, there is a need to find methods that provide a marker unique to PM and allow for higher accuracy of PM diagnosis and consequently the treatment of the disease. Continuing, in this study, we used Raman spectroscopy, Principal Components Analysis (PCA), and Partial Least Squares (PLS) analysis as helpful diagnostic tools for PM. Consequently, we used serum collected from PM patients, which were classified using clinical parameters of PM such as the dynamic international prognostic scoring system (DIPSS) for primary myelofibrosis plus score, the JAK2V617F mutation, spleen size, bone marrow reticulin fibrosis degree and use of hydroxyurea drug features. Raman spectra showed higher amounts of C-H, C-C and C-C/C-N and amide II and lower amounts of amide I and vibrations of CH3 groups in PM patients than in healthy ones. Furthermore, shifts of amides II and I vibrations in PM patients were noticed. Machine learning methods were used to analyze Raman regions: (i) 800 cm−1 and 1800 cm−1, (ii) 1600 cm−1–1700 cm−1, and (iii) 2700 cm−1–3000 cm−1 showed 100 % accuracy, sensitivity, and specificity. Differences in the spectral dynamic showed that differences in the amide II and amide I regions were the most significant in distinguishing between PM and healthy subjects. Importantly, until now, the efficacy of Raman spectroscopy has not been established in clinical diagnostics of PM disease using the correlation between Raman spectra and PM clinical prognostic scoring. Continuing, our results showed the correlation between Raman signals and bone marrow fibrosis, as well as JAKV617F. Consequently, the results revealed that Raman spectroscopy has a high potential for use in medical laboratory diagnostics to quantify multiple biomarkers simultaneously, especially in the selected Raman regions.
Herein, a comparative analysis of clinical prognostic scores, with a novel assessment of serum, was conducted by Raman spectroscopy application to PM vs. healthy subjects. Variables with a VIP score greater than 1 are |
doi_str_mv | 10.1016/j.nano.2023.102706 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2857849037</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1549963423000576</els_id><sourcerecordid>2857849037</sourcerecordid><originalsourceid>FETCH-LOGICAL-c284t-e36ae84f536d1ac12119a3fce908b48f42e3eaa7186d20c0e6d9f6038fa8e3d13</originalsourceid><addsrcrecordid>eNp9kc9OGzEQxldVkUqBF-jJRy5J_Wez8apcKgotElIlBGdrYo-Tibz21t5Q5UF4X5wG9chprNH3m_F8X9N8EXwuuOi-bucRYppLLlVtyCXvPjSnYtH2s75r5cf_b9V-aj6XsuVcLTnvT5uXHzihnShFljwbMw2Q92zYY0ieVjkVKowiW4WUHCuYdwN7JmAPMEBkZaxo1dg07hmUqp3QsVXlwW4oIgsIOVJcMxjHnGoTyzdmU84Y4N_OvzRtmA0UyUJgjmAdDyvPmxMPoeDFWz1rnm5vHq9_ze5__7y7_n4_s1K30wxVB6hbv1CdE2CFFKIH5S32XK9a7VuJCgGWQndOcsuxc73vuNIeNCon1FlzeZxbf_dnh2UyAxWLIUDEtCtG6sVSt301q0rlUWrrwSWjN29mGcHNIQOzNYcMzCEDc8ygQldHCOsRz4TZFEsYLTrK1TrjEr2HvwIrgpRx</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2857849037</pqid></control><display><type>article</type><title>Detection of primary myelofibrosis in blood serum via Raman spectroscopy assisted by machine learning approaches; correlation with clinical diagnosis</title><source>Elsevier ScienceDirect Journals Complete</source><creator>Guleken, Zozan ; Ceylan, Zeynep ; Aday, Aynur ; Bayrak, Ayşe Gül ; Hindilerden, İpek Yönal ; Nalçacı, Meliha ; Jakubczyk, Paweł ; Jakubczyk, Dorota ; Kula-Maximenko, Monika ; Depciuch, Joanna</creator><creatorcontrib>Guleken, Zozan ; Ceylan, Zeynep ; Aday, Aynur ; Bayrak, Ayşe Gül ; Hindilerden, İpek Yönal ; Nalçacı, Meliha ; Jakubczyk, Paweł ; Jakubczyk, Dorota ; Kula-Maximenko, Monika ; Depciuch, Joanna</creatorcontrib><description>Primary myelofibrosis (PM) is one of the myeloproliferative neoplasm, where stem cell-derived clonal neoplasms was noticed. Diagnosis of this disease is based on: physical examination, peripheral blood findings, bone marrow morphology, cytogenetics, and molecular markers. However, the molecular marker of PM, which is a mutation in the JAK2V617F gene, was observed also in other myeloproliferative neoplasms such as polycythemia vera and essential thrombocythemia. Therefore, there is a need to find methods that provide a marker unique to PM and allow for higher accuracy of PM diagnosis and consequently the treatment of the disease. Continuing, in this study, we used Raman spectroscopy, Principal Components Analysis (PCA), and Partial Least Squares (PLS) analysis as helpful diagnostic tools for PM. Consequently, we used serum collected from PM patients, which were classified using clinical parameters of PM such as the dynamic international prognostic scoring system (DIPSS) for primary myelofibrosis plus score, the JAK2V617F mutation, spleen size, bone marrow reticulin fibrosis degree and use of hydroxyurea drug features. Raman spectra showed higher amounts of C-H, C-C and C-C/C-N and amide II and lower amounts of amide I and vibrations of CH3 groups in PM patients than in healthy ones. Furthermore, shifts of amides II and I vibrations in PM patients were noticed. Machine learning methods were used to analyze Raman regions: (i) 800 cm−1 and 1800 cm−1, (ii) 1600 cm−1–1700 cm−1, and (iii) 2700 cm−1–3000 cm−1 showed 100 % accuracy, sensitivity, and specificity. Differences in the spectral dynamic showed that differences in the amide II and amide I regions were the most significant in distinguishing between PM and healthy subjects. Importantly, until now, the efficacy of Raman spectroscopy has not been established in clinical diagnostics of PM disease using the correlation between Raman spectra and PM clinical prognostic scoring. Continuing, our results showed the correlation between Raman signals and bone marrow fibrosis, as well as JAKV617F. Consequently, the results revealed that Raman spectroscopy has a high potential for use in medical laboratory diagnostics to quantify multiple biomarkers simultaneously, especially in the selected Raman regions.
Herein, a comparative analysis of clinical prognostic scores, with a novel assessment of serum, was conducted by Raman spectroscopy application to PM vs. healthy subjects. Variables with a VIP score greater than 1 are considered important for the projection of the PLS regression model. Machine learning methods discriminated regions with 100 % accuracy, sensitivity, and specificity. Differences in the spectra dynamic showed, that differences in the amide II and amide I were the most significant in differentiation PM and healthy subjects. Finally, correlation between Raman signals and bone marrow fibrosis, as well as JAKV617 was existed. Consequently, the results reveal, that Raman spectroscopy has a high potential for use in medical laboratory diagnostics to quantify multiple biomarkers simultaneously, especially in the selected Raman regions. [Display omitted]
•Shifts of amide II and amide I vibrations in PM Raman spectra•Correlation between bone marrow fibrosis, JAKV617, and Raman signals•Amide I and amide II regions as significant Raman markers of PM•The accuracy of Raman spectroscopy is around 100 %.</description><identifier>ISSN: 1549-9634</identifier><identifier>EISSN: 1549-9642</identifier><identifier>DOI: 10.1016/j.nano.2023.102706</identifier><language>eng</language><publisher>Elsevier Inc</publisher><subject>Jak2 mutation ; Machine learning ; Partial least squares (PLS) ; Primary myelofibrosis ; Principal components analysis (PCA) ; Raman</subject><ispartof>Nanomedicine, 2023-09, Vol.53, p.102706-102706, Article 102706</ispartof><rights>2023 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c284t-e36ae84f536d1ac12119a3fce908b48f42e3eaa7186d20c0e6d9f6038fa8e3d13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.nano.2023.102706$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids></links><search><creatorcontrib>Guleken, Zozan</creatorcontrib><creatorcontrib>Ceylan, Zeynep</creatorcontrib><creatorcontrib>Aday, Aynur</creatorcontrib><creatorcontrib>Bayrak, Ayşe Gül</creatorcontrib><creatorcontrib>Hindilerden, İpek Yönal</creatorcontrib><creatorcontrib>Nalçacı, Meliha</creatorcontrib><creatorcontrib>Jakubczyk, Paweł</creatorcontrib><creatorcontrib>Jakubczyk, Dorota</creatorcontrib><creatorcontrib>Kula-Maximenko, Monika</creatorcontrib><creatorcontrib>Depciuch, Joanna</creatorcontrib><title>Detection of primary myelofibrosis in blood serum via Raman spectroscopy assisted by machine learning approaches; correlation with clinical diagnosis</title><title>Nanomedicine</title><description>Primary myelofibrosis (PM) is one of the myeloproliferative neoplasm, where stem cell-derived clonal neoplasms was noticed. Diagnosis of this disease is based on: physical examination, peripheral blood findings, bone marrow morphology, cytogenetics, and molecular markers. However, the molecular marker of PM, which is a mutation in the JAK2V617F gene, was observed also in other myeloproliferative neoplasms such as polycythemia vera and essential thrombocythemia. Therefore, there is a need to find methods that provide a marker unique to PM and allow for higher accuracy of PM diagnosis and consequently the treatment of the disease. Continuing, in this study, we used Raman spectroscopy, Principal Components Analysis (PCA), and Partial Least Squares (PLS) analysis as helpful diagnostic tools for PM. Consequently, we used serum collected from PM patients, which were classified using clinical parameters of PM such as the dynamic international prognostic scoring system (DIPSS) for primary myelofibrosis plus score, the JAK2V617F mutation, spleen size, bone marrow reticulin fibrosis degree and use of hydroxyurea drug features. Raman spectra showed higher amounts of C-H, C-C and C-C/C-N and amide II and lower amounts of amide I and vibrations of CH3 groups in PM patients than in healthy ones. Furthermore, shifts of amides II and I vibrations in PM patients were noticed. Machine learning methods were used to analyze Raman regions: (i) 800 cm−1 and 1800 cm−1, (ii) 1600 cm−1–1700 cm−1, and (iii) 2700 cm−1–3000 cm−1 showed 100 % accuracy, sensitivity, and specificity. Differences in the spectral dynamic showed that differences in the amide II and amide I regions were the most significant in distinguishing between PM and healthy subjects. Importantly, until now, the efficacy of Raman spectroscopy has not been established in clinical diagnostics of PM disease using the correlation between Raman spectra and PM clinical prognostic scoring. Continuing, our results showed the correlation between Raman signals and bone marrow fibrosis, as well as JAKV617F. Consequently, the results revealed that Raman spectroscopy has a high potential for use in medical laboratory diagnostics to quantify multiple biomarkers simultaneously, especially in the selected Raman regions.
Herein, a comparative analysis of clinical prognostic scores, with a novel assessment of serum, was conducted by Raman spectroscopy application to PM vs. healthy subjects. Variables with a VIP score greater than 1 are considered important for the projection of the PLS regression model. Machine learning methods discriminated regions with 100 % accuracy, sensitivity, and specificity. Differences in the spectra dynamic showed, that differences in the amide II and amide I were the most significant in differentiation PM and healthy subjects. Finally, correlation between Raman signals and bone marrow fibrosis, as well as JAKV617 was existed. Consequently, the results reveal, that Raman spectroscopy has a high potential for use in medical laboratory diagnostics to quantify multiple biomarkers simultaneously, especially in the selected Raman regions. [Display omitted]
•Shifts of amide II and amide I vibrations in PM Raman spectra•Correlation between bone marrow fibrosis, JAKV617, and Raman signals•Amide I and amide II regions as significant Raman markers of PM•The accuracy of Raman spectroscopy is around 100 %.</description><subject>Jak2 mutation</subject><subject>Machine learning</subject><subject>Partial least squares (PLS)</subject><subject>Primary myelofibrosis</subject><subject>Principal components analysis (PCA)</subject><subject>Raman</subject><issn>1549-9634</issn><issn>1549-9642</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kc9OGzEQxldVkUqBF-jJRy5J_Wez8apcKgotElIlBGdrYo-Tibz21t5Q5UF4X5wG9chprNH3m_F8X9N8EXwuuOi-bucRYppLLlVtyCXvPjSnYtH2s75r5cf_b9V-aj6XsuVcLTnvT5uXHzihnShFljwbMw2Q92zYY0ieVjkVKowiW4WUHCuYdwN7JmAPMEBkZaxo1dg07hmUqp3QsVXlwW4oIgsIOVJcMxjHnGoTyzdmU84Y4N_OvzRtmA0UyUJgjmAdDyvPmxMPoeDFWz1rnm5vHq9_ze5__7y7_n4_s1K30wxVB6hbv1CdE2CFFKIH5S32XK9a7VuJCgGWQndOcsuxc73vuNIeNCon1FlzeZxbf_dnh2UyAxWLIUDEtCtG6sVSt301q0rlUWrrwSWjN29mGcHNIQOzNYcMzCEDc8ygQldHCOsRz4TZFEsYLTrK1TrjEr2HvwIrgpRx</recordid><startdate>202309</startdate><enddate>202309</enddate><creator>Guleken, Zozan</creator><creator>Ceylan, Zeynep</creator><creator>Aday, Aynur</creator><creator>Bayrak, Ayşe Gül</creator><creator>Hindilerden, İpek Yönal</creator><creator>Nalçacı, Meliha</creator><creator>Jakubczyk, Paweł</creator><creator>Jakubczyk, Dorota</creator><creator>Kula-Maximenko, Monika</creator><creator>Depciuch, Joanna</creator><general>Elsevier Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202309</creationdate><title>Detection of primary myelofibrosis in blood serum via Raman spectroscopy assisted by machine learning approaches; correlation with clinical diagnosis</title><author>Guleken, Zozan ; Ceylan, Zeynep ; Aday, Aynur ; Bayrak, Ayşe Gül ; Hindilerden, İpek Yönal ; Nalçacı, Meliha ; Jakubczyk, Paweł ; Jakubczyk, Dorota ; Kula-Maximenko, Monika ; Depciuch, Joanna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c284t-e36ae84f536d1ac12119a3fce908b48f42e3eaa7186d20c0e6d9f6038fa8e3d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Jak2 mutation</topic><topic>Machine learning</topic><topic>Partial least squares (PLS)</topic><topic>Primary myelofibrosis</topic><topic>Principal components analysis (PCA)</topic><topic>Raman</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guleken, Zozan</creatorcontrib><creatorcontrib>Ceylan, Zeynep</creatorcontrib><creatorcontrib>Aday, Aynur</creatorcontrib><creatorcontrib>Bayrak, Ayşe Gül</creatorcontrib><creatorcontrib>Hindilerden, İpek Yönal</creatorcontrib><creatorcontrib>Nalçacı, Meliha</creatorcontrib><creatorcontrib>Jakubczyk, Paweł</creatorcontrib><creatorcontrib>Jakubczyk, Dorota</creatorcontrib><creatorcontrib>Kula-Maximenko, Monika</creatorcontrib><creatorcontrib>Depciuch, Joanna</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Nanomedicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guleken, Zozan</au><au>Ceylan, Zeynep</au><au>Aday, Aynur</au><au>Bayrak, Ayşe Gül</au><au>Hindilerden, İpek Yönal</au><au>Nalçacı, Meliha</au><au>Jakubczyk, Paweł</au><au>Jakubczyk, Dorota</au><au>Kula-Maximenko, Monika</au><au>Depciuch, Joanna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of primary myelofibrosis in blood serum via Raman spectroscopy assisted by machine learning approaches; correlation with clinical diagnosis</atitle><jtitle>Nanomedicine</jtitle><date>2023-09</date><risdate>2023</risdate><volume>53</volume><spage>102706</spage><epage>102706</epage><pages>102706-102706</pages><artnum>102706</artnum><issn>1549-9634</issn><eissn>1549-9642</eissn><abstract>Primary myelofibrosis (PM) is one of the myeloproliferative neoplasm, where stem cell-derived clonal neoplasms was noticed. Diagnosis of this disease is based on: physical examination, peripheral blood findings, bone marrow morphology, cytogenetics, and molecular markers. However, the molecular marker of PM, which is a mutation in the JAK2V617F gene, was observed also in other myeloproliferative neoplasms such as polycythemia vera and essential thrombocythemia. Therefore, there is a need to find methods that provide a marker unique to PM and allow for higher accuracy of PM diagnosis and consequently the treatment of the disease. Continuing, in this study, we used Raman spectroscopy, Principal Components Analysis (PCA), and Partial Least Squares (PLS) analysis as helpful diagnostic tools for PM. Consequently, we used serum collected from PM patients, which were classified using clinical parameters of PM such as the dynamic international prognostic scoring system (DIPSS) for primary myelofibrosis plus score, the JAK2V617F mutation, spleen size, bone marrow reticulin fibrosis degree and use of hydroxyurea drug features. Raman spectra showed higher amounts of C-H, C-C and C-C/C-N and amide II and lower amounts of amide I and vibrations of CH3 groups in PM patients than in healthy ones. Furthermore, shifts of amides II and I vibrations in PM patients were noticed. Machine learning methods were used to analyze Raman regions: (i) 800 cm−1 and 1800 cm−1, (ii) 1600 cm−1–1700 cm−1, and (iii) 2700 cm−1–3000 cm−1 showed 100 % accuracy, sensitivity, and specificity. Differences in the spectral dynamic showed that differences in the amide II and amide I regions were the most significant in distinguishing between PM and healthy subjects. Importantly, until now, the efficacy of Raman spectroscopy has not been established in clinical diagnostics of PM disease using the correlation between Raman spectra and PM clinical prognostic scoring. Continuing, our results showed the correlation between Raman signals and bone marrow fibrosis, as well as JAKV617F. Consequently, the results revealed that Raman spectroscopy has a high potential for use in medical laboratory diagnostics to quantify multiple biomarkers simultaneously, especially in the selected Raman regions.
Herein, a comparative analysis of clinical prognostic scores, with a novel assessment of serum, was conducted by Raman spectroscopy application to PM vs. healthy subjects. Variables with a VIP score greater than 1 are considered important for the projection of the PLS regression model. Machine learning methods discriminated regions with 100 % accuracy, sensitivity, and specificity. Differences in the spectra dynamic showed, that differences in the amide II and amide I were the most significant in differentiation PM and healthy subjects. Finally, correlation between Raman signals and bone marrow fibrosis, as well as JAKV617 was existed. Consequently, the results reveal, that Raman spectroscopy has a high potential for use in medical laboratory diagnostics to quantify multiple biomarkers simultaneously, especially in the selected Raman regions. [Display omitted]
•Shifts of amide II and amide I vibrations in PM Raman spectra•Correlation between bone marrow fibrosis, JAKV617, and Raman signals•Amide I and amide II regions as significant Raman markers of PM•The accuracy of Raman spectroscopy is around 100 %.</abstract><pub>Elsevier Inc</pub><doi>10.1016/j.nano.2023.102706</doi><tpages>1</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1549-9634 |
ispartof | Nanomedicine, 2023-09, Vol.53, p.102706-102706, Article 102706 |
issn | 1549-9634 1549-9642 |
language | eng |
recordid | cdi_proquest_miscellaneous_2857849037 |
source | Elsevier ScienceDirect Journals Complete |
subjects | Jak2 mutation Machine learning Partial least squares (PLS) Primary myelofibrosis Principal components analysis (PCA) Raman |
title | Detection of primary myelofibrosis in blood serum via Raman spectroscopy assisted by machine learning approaches; correlation with clinical diagnosis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T06%3A02%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Detection%20of%20primary%20myelofibrosis%20in%20blood%20serum%20via%20Raman%20spectroscopy%20assisted%20by%20machine%20learning%20approaches;%20correlation%20with%20clinical%20diagnosis&rft.jtitle=Nanomedicine&rft.au=Guleken,%20Zozan&rft.date=2023-09&rft.volume=53&rft.spage=102706&rft.epage=102706&rft.pages=102706-102706&rft.artnum=102706&rft.issn=1549-9634&rft.eissn=1549-9642&rft_id=info:doi/10.1016/j.nano.2023.102706&rft_dat=%3Cproquest_cross%3E2857849037%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2857849037&rft_id=info:pmid/&rft_els_id=S1549963423000576&rfr_iscdi=true |