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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nanomedicine 2023-09, Vol.53, p.102706-102706, Article 102706
Hauptverfasser: Guleken, Zozan, Ceylan, Zeynep, Aday, Aynur, Bayrak, Ayşe Gül, Hindilerden, İpek Yönal, Nalçacı, Meliha, Jakubczyk, Paweł, Jakubczyk, Dorota, Kula-Maximenko, Monika, Depciuch, Joanna
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