Peritumoral ADC Values Correlate with the MGMT Methylation Status in Patients with Glioblastoma
Different results have been reported concerning the relationship of the apparent diffusion coefficient (ADC) values and the status of methylation as the promoter gene for the enzyme methylguanine-DNA methyltransferase (MGMT) in patients with glioblastomas (GBs). The aim of this study was to investig...
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Veröffentlicht in: | Cancers 2023-02, Vol.15 (5), p.1384 |
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creator | Ladenhauf, Valentin Karl Galijasevic, Malik Kerschbaumer, Johannes Freyschlag, Christian Franz Nowosielski, Martha Birkl-Toeglhofer, Anna Maria Haybaeck, Johannes Gizewski, Elke Ruth Mangesius, Stephanie Grams, Astrid Ellen |
description | Different results have been reported concerning the relationship of the apparent diffusion coefficient (ADC) values and the status of methylation as the promoter gene for the enzyme methylguanine-DNA methyltransferase (MGMT) in patients with glioblastomas (GBs). The aim of this study was to investigate if there were correlations between the ADC values of the enhancing tumor and peritumoral areas of GBs and the MGMT methylation status. In this retrospective study, we included 42 patients with newly diagnosed unilocular GB with one MRI study prior to any treatment and histopathological data. After co-registration of ADC maps with T1-weighted sequences after contrast administration and dynamic susceptibility contrast (DSC) perfusion, we manually selected one region-of-interest (ROI) in the enhancing and perfused tumor and one ROI in the peritumoral white matter. Both ROIs were mirrored in the healthy hemisphere for normalization. In the peritumoral white matter, absolute and normalized ADC values were significantly higher in patients with MGMT-unmethylated tumors, as compared to patients with MGMT-methylated tumors (absolute values
= 0.002, normalized
= 0.0007). There were no significant differences in the enhancing tumor parts. The ADC values in the peritumoral region correlated with MGMT methylation status, confirmed by normalized ADC values. In contrast to other studies, we could not find a correlation between the ADC values or the normalized ADC values and the MGMT methylation status in the enhancing tumor parts. |
doi_str_mv | 10.3390/cancers15051384 |
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= 0.002, normalized
= 0.0007). There were no significant differences in the enhancing tumor parts. The ADC values in the peritumoral region correlated with MGMT methylation status, confirmed by normalized ADC values. In contrast to other studies, we could not find a correlation between the ADC values or the normalized ADC values and the MGMT methylation status in the enhancing tumor parts.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers15051384</identifier><identifier>PMID: 36900177</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Biopsy ; Diagnosis ; Diffusion coefficient ; DNA methylation ; DNA methyltransferase ; Edema ; Gene mapping ; Glioblastoma ; Glioblastoma multiforme ; Health aspects ; Magnetic resonance imaging ; Medical prognosis ; Methods ; Methylation ; Methylguanine ; Methyltransferases ; Nervous system ; Neuropathology ; O6-methylguanine-DNA methyltransferase ; Patients ; Statistical analysis ; Substantia alba ; Tumors</subject><ispartof>Cancers, 2023-02, Vol.15 (5), p.1384</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c489t-dd87972def372c7aeec9d8fdf8d1b4aa35094ddc06a33fd10fb7393abacadbb53</citedby><cites>FETCH-LOGICAL-c489t-dd87972def372c7aeec9d8fdf8d1b4aa35094ddc06a33fd10fb7393abacadbb53</cites><orcidid>0000-0001-6859-8377 ; 0000-0001-6577-0784 ; 0000-0002-9997-4336 ; 0000-0001-6908-145X ; 0000-0001-5518-3359 ; 0000-0002-8228-8217 ; 0000-0001-5790-2724 ; 0000-0002-8068-315X ; 0000-0003-2304-3946</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000073/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000073/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36900177$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ladenhauf, Valentin Karl</creatorcontrib><creatorcontrib>Galijasevic, Malik</creatorcontrib><creatorcontrib>Kerschbaumer, Johannes</creatorcontrib><creatorcontrib>Freyschlag, Christian Franz</creatorcontrib><creatorcontrib>Nowosielski, Martha</creatorcontrib><creatorcontrib>Birkl-Toeglhofer, Anna Maria</creatorcontrib><creatorcontrib>Haybaeck, Johannes</creatorcontrib><creatorcontrib>Gizewski, Elke Ruth</creatorcontrib><creatorcontrib>Mangesius, Stephanie</creatorcontrib><creatorcontrib>Grams, Astrid Ellen</creatorcontrib><title>Peritumoral ADC Values Correlate with the MGMT Methylation Status in Patients with Glioblastoma</title><title>Cancers</title><addtitle>Cancers (Basel)</addtitle><description>Different results have been reported concerning the relationship of the apparent diffusion coefficient (ADC) values and the status of methylation as the promoter gene for the enzyme methylguanine-DNA methyltransferase (MGMT) in patients with glioblastomas (GBs). The aim of this study was to investigate if there were correlations between the ADC values of the enhancing tumor and peritumoral areas of GBs and the MGMT methylation status. In this retrospective study, we included 42 patients with newly diagnosed unilocular GB with one MRI study prior to any treatment and histopathological data. After co-registration of ADC maps with T1-weighted sequences after contrast administration and dynamic susceptibility contrast (DSC) perfusion, we manually selected one region-of-interest (ROI) in the enhancing and perfused tumor and one ROI in the peritumoral white matter. Both ROIs were mirrored in the healthy hemisphere for normalization. In the peritumoral white matter, absolute and normalized ADC values were significantly higher in patients with MGMT-unmethylated tumors, as compared to patients with MGMT-methylated tumors (absolute values
= 0.002, normalized
= 0.0007). There were no significant differences in the enhancing tumor parts. The ADC values in the peritumoral region correlated with MGMT methylation status, confirmed by normalized ADC values. In contrast to other studies, we could not find a correlation between the ADC values or the normalized ADC values and the MGMT methylation status in the enhancing tumor parts.</description><subject>Biopsy</subject><subject>Diagnosis</subject><subject>Diffusion coefficient</subject><subject>DNA methylation</subject><subject>DNA methyltransferase</subject><subject>Edema</subject><subject>Gene mapping</subject><subject>Glioblastoma</subject><subject>Glioblastoma multiforme</subject><subject>Health aspects</subject><subject>Magnetic resonance imaging</subject><subject>Medical prognosis</subject><subject>Methods</subject><subject>Methylation</subject><subject>Methylguanine</subject><subject>Methyltransferases</subject><subject>Nervous system</subject><subject>Neuropathology</subject><subject>O6-methylguanine-DNA methyltransferase</subject><subject>Patients</subject><subject>Statistical analysis</subject><subject>Substantia alba</subject><subject>Tumors</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkkFP3DAQha2qqCDg3FtlqZdeFuw4ieNTtdrSpRKrIpX2ak3sCWuUxNR2ivj3dbRAAdWXWJNvnuc9DSHvOTsRQrFTA6PBEHnFKi6a8g05KJgsFnWtyrfP7vvkOMYblo8QXNbyHdkXtWKMS3lA9CUGl6bBB-jp8suK_oJ-wkhXPgTsISG9c2lL0xbpZr25ohtM2_tcd36kPxKkKVI30stcwDHFHbzunW97iMkPcET2OugjHj98D8nPr2dXq_PFxff1t9XyYmHKRqWFtY1UsrDYCVkYCYhG2aazXWN5WwKIiqnSWsNqEKKznHWtFEpACwZs21bikHze6d5O7YDW5GmyI30b3ADhXntw-uWf0W31tf-j-RwMkyIrfHpQCP53jiDpwUWDfQ8j-inqQjZ1hvMgGf34Cr3xUxizv5mqcsi1qv5R19CjdmPn88NmFtVLWfI8vxJNpk7-Q822cHDGj9i5XH_RcLprMMHHGLB7MsmZnvdCv9qL3PHheTZP_OMWiL-NEbVu</recordid><startdate>20230222</startdate><enddate>20230222</enddate><creator>Ladenhauf, Valentin Karl</creator><creator>Galijasevic, Malik</creator><creator>Kerschbaumer, Johannes</creator><creator>Freyschlag, Christian Franz</creator><creator>Nowosielski, Martha</creator><creator>Birkl-Toeglhofer, Anna Maria</creator><creator>Haybaeck, Johannes</creator><creator>Gizewski, Elke Ruth</creator><creator>Mangesius, Stephanie</creator><creator>Grams, Astrid Ellen</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6859-8377</orcidid><orcidid>https://orcid.org/0000-0001-6577-0784</orcidid><orcidid>https://orcid.org/0000-0002-9997-4336</orcidid><orcidid>https://orcid.org/0000-0001-6908-145X</orcidid><orcidid>https://orcid.org/0000-0001-5518-3359</orcidid><orcidid>https://orcid.org/0000-0002-8228-8217</orcidid><orcidid>https://orcid.org/0000-0001-5790-2724</orcidid><orcidid>https://orcid.org/0000-0002-8068-315X</orcidid><orcidid>https://orcid.org/0000-0003-2304-3946</orcidid></search><sort><creationdate>20230222</creationdate><title>Peritumoral ADC Values Correlate with the MGMT Methylation Status in Patients with Glioblastoma</title><author>Ladenhauf, Valentin Karl ; Galijasevic, Malik ; Kerschbaumer, Johannes ; Freyschlag, Christian Franz ; Nowosielski, Martha ; Birkl-Toeglhofer, Anna Maria ; Haybaeck, Johannes ; Gizewski, Elke Ruth ; Mangesius, Stephanie ; Grams, Astrid Ellen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c489t-dd87972def372c7aeec9d8fdf8d1b4aa35094ddc06a33fd10fb7393abacadbb53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Biopsy</topic><topic>Diagnosis</topic><topic>Diffusion coefficient</topic><topic>DNA methylation</topic><topic>DNA methyltransferase</topic><topic>Edema</topic><topic>Gene mapping</topic><topic>Glioblastoma</topic><topic>Glioblastoma multiforme</topic><topic>Health aspects</topic><topic>Magnetic resonance imaging</topic><topic>Medical prognosis</topic><topic>Methods</topic><topic>Methylation</topic><topic>Methylguanine</topic><topic>Methyltransferases</topic><topic>Nervous system</topic><topic>Neuropathology</topic><topic>O6-methylguanine-DNA methyltransferase</topic><topic>Patients</topic><topic>Statistical analysis</topic><topic>Substantia alba</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ladenhauf, Valentin Karl</creatorcontrib><creatorcontrib>Galijasevic, Malik</creatorcontrib><creatorcontrib>Kerschbaumer, Johannes</creatorcontrib><creatorcontrib>Freyschlag, Christian Franz</creatorcontrib><creatorcontrib>Nowosielski, Martha</creatorcontrib><creatorcontrib>Birkl-Toeglhofer, Anna Maria</creatorcontrib><creatorcontrib>Haybaeck, Johannes</creatorcontrib><creatorcontrib>Gizewski, Elke Ruth</creatorcontrib><creatorcontrib>Mangesius, Stephanie</creatorcontrib><creatorcontrib>Grams, Astrid Ellen</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ladenhauf, Valentin Karl</au><au>Galijasevic, Malik</au><au>Kerschbaumer, Johannes</au><au>Freyschlag, Christian Franz</au><au>Nowosielski, Martha</au><au>Birkl-Toeglhofer, Anna Maria</au><au>Haybaeck, Johannes</au><au>Gizewski, Elke Ruth</au><au>Mangesius, Stephanie</au><au>Grams, Astrid Ellen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Peritumoral ADC Values Correlate with the MGMT Methylation Status in Patients with Glioblastoma</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2023-02-22</date><risdate>2023</risdate><volume>15</volume><issue>5</issue><spage>1384</spage><pages>1384-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>Different results have been reported concerning the relationship of the apparent diffusion coefficient (ADC) values and the status of methylation as the promoter gene for the enzyme methylguanine-DNA methyltransferase (MGMT) in patients with glioblastomas (GBs). The aim of this study was to investigate if there were correlations between the ADC values of the enhancing tumor and peritumoral areas of GBs and the MGMT methylation status. In this retrospective study, we included 42 patients with newly diagnosed unilocular GB with one MRI study prior to any treatment and histopathological data. After co-registration of ADC maps with T1-weighted sequences after contrast administration and dynamic susceptibility contrast (DSC) perfusion, we manually selected one region-of-interest (ROI) in the enhancing and perfused tumor and one ROI in the peritumoral white matter. Both ROIs were mirrored in the healthy hemisphere for normalization. In the peritumoral white matter, absolute and normalized ADC values were significantly higher in patients with MGMT-unmethylated tumors, as compared to patients with MGMT-methylated tumors (absolute values
= 0.002, normalized
= 0.0007). There were no significant differences in the enhancing tumor parts. The ADC values in the peritumoral region correlated with MGMT methylation status, confirmed by normalized ADC values. In contrast to other studies, we could not find a correlation between the ADC values or the normalized ADC values and the MGMT methylation status in the enhancing tumor parts.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>36900177</pmid><doi>10.3390/cancers15051384</doi><orcidid>https://orcid.org/0000-0001-6859-8377</orcidid><orcidid>https://orcid.org/0000-0001-6577-0784</orcidid><orcidid>https://orcid.org/0000-0002-9997-4336</orcidid><orcidid>https://orcid.org/0000-0001-6908-145X</orcidid><orcidid>https://orcid.org/0000-0001-5518-3359</orcidid><orcidid>https://orcid.org/0000-0002-8228-8217</orcidid><orcidid>https://orcid.org/0000-0001-5790-2724</orcidid><orcidid>https://orcid.org/0000-0002-8068-315X</orcidid><orcidid>https://orcid.org/0000-0003-2304-3946</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biopsy Diagnosis Diffusion coefficient DNA methylation DNA methyltransferase Edema Gene mapping Glioblastoma Glioblastoma multiforme Health aspects Magnetic resonance imaging Medical prognosis Methods Methylation Methylguanine Methyltransferases Nervous system Neuropathology O6-methylguanine-DNA methyltransferase Patients Statistical analysis Substantia alba Tumors |
title | Peritumoral ADC Values Correlate with the MGMT Methylation Status in Patients with Glioblastoma |
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