In vitro high resolution 1h-spectroscopy of the human prostate: Benign prostatic hyperplasia, normal peripheral zone and adenocarcinoma

1H‐spectra at 360 MHz from perchloric extracts of 35 human prostate specimens were obtained. First, we sought to define what peaks can be assigned in vitro, and thus, potentially seen in vivo. Second, we sought to try to discriminate between adenocarcinoma, normal peripheral zone and benign prostati...

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Veröffentlicht in:Magnetic resonance in medicine 1993-03, Vol.29 (3), p.285-291
Hauptverfasser: Schiebler, Mark L., Miyamoto, Kent K., White, Mark, Maygarden, Susan J., Mohler, James L.
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container_end_page 291
container_issue 3
container_start_page 285
container_title Magnetic resonance in medicine
container_volume 29
creator Schiebler, Mark L.
Miyamoto, Kent K.
White, Mark
Maygarden, Susan J.
Mohler, James L.
description 1H‐spectra at 360 MHz from perchloric extracts of 35 human prostate specimens were obtained. First, we sought to define what peaks can be assigned in vitro, and thus, potentially seen in vivo. Second, we sought to try to discriminate between adenocarcinoma, normal peripheral zone and benign prostatic hyperplasia using spectral fingerprints. Thirteen samples of adenocarcinoma, 11 samples of benign prostatic hyperplasia, and 11 samples of normal contralateral peripheral zone were analyzed by obtaining a ratio from the maximum area of each major peak and the area of an added standard (3‐trimethyl‐silyl‐propionic acid). There was a significantly larger benign prostate hyperplasia citrate standardized peak area when compared to the adenocarcinoma citrate standardized peak area for each patient (P < 0.05). However, the citrate standardized peak areas from the normal peripheral zones were not significantly different from those found in the adenocarcino‐mas. Four out of 13 cases of stromal hyperplasia had similarly low levels of citrate as their respective gland's adenocarcinoma. We also found a sharp peak at 2.05 ppm that was seen in 4 out of 13 adenocarcinoma samples and in only 1 out of 13 of the benign prostate hypertrophy samples which has tentatively been assigned to N‐acetyl neuraminic acid. Further studies are required to assess whether low citrate levels alone can serve to exclusively diagnose adenocarcinoma of the prostate.
doi_str_mv 10.1002/mrm.1910290302
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We also found a sharp peak at 2.05 ppm that was seen in 4 out of 13 adenocarcinoma samples and in only 1 out of 13 of the benign prostate hypertrophy samples which has tentatively been assigned to N‐acetyl neuraminic acid. 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Reson. Med</addtitle><description>1H‐spectra at 360 MHz from perchloric extracts of 35 human prostate specimens were obtained. First, we sought to define what peaks can be assigned in vitro, and thus, potentially seen in vivo. Second, we sought to try to discriminate between adenocarcinoma, normal peripheral zone and benign prostatic hyperplasia using spectral fingerprints. Thirteen samples of adenocarcinoma, 11 samples of benign prostatic hyperplasia, and 11 samples of normal contralateral peripheral zone were analyzed by obtaining a ratio from the maximum area of each major peak and the area of an added standard (3‐trimethyl‐silyl‐propionic acid). There was a significantly larger benign prostate hyperplasia citrate standardized peak area when compared to the adenocarcinoma citrate standardized peak area for each patient (P &lt; 0.05). However, the citrate standardized peak areas from the normal peripheral zones were not significantly different from those found in the adenocarcino‐mas. Four out of 13 cases of stromal hyperplasia had similarly low levels of citrate as their respective gland's adenocarcinoma. We also found a sharp peak at 2.05 ppm that was seen in 4 out of 13 adenocarcinoma samples and in only 1 out of 13 of the benign prostate hypertrophy samples which has tentatively been assigned to N‐acetyl neuraminic acid. 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Miscellaneous investigative techniques</subject><subject>prostate</subject><subject>Prostate - chemistry</subject><subject>Prostate - metabolism</subject><subject>Prostate - pathology</subject><subject>Prostatic Hyperplasia - metabolism</subject><subject>Prostatic Hyperplasia - pathology</subject><subject>Prostatic Neoplasms - metabolism</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Sialic Acids - analysis</subject><subject>Sialic Acids - metabolism</subject><subject>spectroscopy</subject><subject>Urinary system</subject><issn>0740-3194</issn><issn>1522-2594</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkUFv1DAUhC0EKtvClRuSD4hTU-zYjmNupYLSqgsSWqjExXKcl8aQ2MFOgOUP8Lcx2tX25Of5ZizrDULPKDmjhJSvxjieUUVJqQgj5QO0oqIsi1Io_hCtiOSkYFTxx-g4pW-EEKUkP0JHsqozq1bo75XHP90cA-7dXY8jpDAsswse075IE9iMkg3TFocOzz3gfhmNx1NWZzPDa_wGvLs7CM7ifjtBnAaTnDnFPsTRDDgrbuoh5vFP8ICNb7FpwQdronU-jOYJetSZIcHT_XmCPr97u7l4X9x8vLy6OL8pHJWkLKqGcMIaChVQxlUtKWGqVdAAEZxy0TDataKGSoCpRUdVbRro2s5S2yoia3aCXu7ezR_-sUCa9eiShWEwHsKStBRVWVdMZOPzvXFpRmj1FN1o4lbvN5f5iz03yZqhi8Zblw42XpVK8DLb1M72yw2wPWBK9P_2dG5P37en15_W97ecLXZZl2b4fcia-F1Xkkmhbz9c6uvN9e366xepN-wfBdOfzQ</recordid><startdate>199303</startdate><enddate>199303</enddate><creator>Schiebler, Mark L.</creator><creator>Miyamoto, Kent K.</creator><creator>White, Mark</creator><creator>Maygarden, Susan J.</creator><creator>Mohler, James L.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Williams &amp; Wilkins</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>199303</creationdate><title>In vitro high resolution 1h-spectroscopy of the human prostate: Benign prostatic hyperplasia, normal peripheral zone and adenocarcinoma</title><author>Schiebler, Mark L. ; Miyamoto, Kent K. ; White, Mark ; Maygarden, Susan J. ; Mohler, James L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i1702-6b0403b1e6e1349871039d9ebe054145b31fd58e65ea85f198abefdfc1cd90783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Acetates - analysis</topic><topic>Acetates - metabolism</topic><topic>adenocarcinoma</topic><topic>Adenocarcinoma - metabolism</topic><topic>Adenocarcinoma - pathology</topic><topic>benign prostatic hyperplasia</topic><topic>Biological and medical sciences</topic><topic>Citrates - analysis</topic><topic>Citrates - metabolism</topic><topic>Glutamates - analysis</topic><topic>Glutamates - metabolism</topic><topic>Humans</topic><topic>Hydrogen</topic><topic>Inositol - analysis</topic><topic>Inositol - metabolism</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Lactates - analysis</topic><topic>Lactates - metabolism</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>N-Acetylneuraminic Acid</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>prostate</topic><topic>Prostate - chemistry</topic><topic>Prostate - metabolism</topic><topic>Prostate - pathology</topic><topic>Prostatic Hyperplasia - metabolism</topic><topic>Prostatic Hyperplasia - pathology</topic><topic>Prostatic Neoplasms - metabolism</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Sialic Acids - analysis</topic><topic>Sialic Acids - metabolism</topic><topic>spectroscopy</topic><topic>Urinary system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schiebler, Mark L.</creatorcontrib><creatorcontrib>Miyamoto, Kent K.</creatorcontrib><creatorcontrib>White, Mark</creatorcontrib><creatorcontrib>Maygarden, Susan J.</creatorcontrib><creatorcontrib>Mohler, James L.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Magnetic resonance in medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schiebler, Mark L.</au><au>Miyamoto, Kent K.</au><au>White, Mark</au><au>Maygarden, Susan J.</au><au>Mohler, James L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro high resolution 1h-spectroscopy of the human prostate: Benign prostatic hyperplasia, normal peripheral zone and adenocarcinoma</atitle><jtitle>Magnetic resonance in medicine</jtitle><addtitle>Magn. Reson. Med</addtitle><date>1993-03</date><risdate>1993</risdate><volume>29</volume><issue>3</issue><spage>285</spage><epage>291</epage><pages>285-291</pages><issn>0740-3194</issn><eissn>1522-2594</eissn><coden>MRMEEN</coden><abstract>1H‐spectra at 360 MHz from perchloric extracts of 35 human prostate specimens were obtained. First, we sought to define what peaks can be assigned in vitro, and thus, potentially seen in vivo. Second, we sought to try to discriminate between adenocarcinoma, normal peripheral zone and benign prostatic hyperplasia using spectral fingerprints. Thirteen samples of adenocarcinoma, 11 samples of benign prostatic hyperplasia, and 11 samples of normal contralateral peripheral zone were analyzed by obtaining a ratio from the maximum area of each major peak and the area of an added standard (3‐trimethyl‐silyl‐propionic acid). There was a significantly larger benign prostate hyperplasia citrate standardized peak area when compared to the adenocarcinoma citrate standardized peak area for each patient (P &lt; 0.05). However, the citrate standardized peak areas from the normal peripheral zones were not significantly different from those found in the adenocarcino‐mas. Four out of 13 cases of stromal hyperplasia had similarly low levels of citrate as their respective gland's adenocarcinoma. We also found a sharp peak at 2.05 ppm that was seen in 4 out of 13 adenocarcinoma samples and in only 1 out of 13 of the benign prostate hypertrophy samples which has tentatively been assigned to N‐acetyl neuraminic acid. Further studies are required to assess whether low citrate levels alone can serve to exclusively diagnose adenocarcinoma of the prostate.</abstract><cop>Baltimore</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>7680746</pmid><doi>10.1002/mrm.1910290302</doi><tpages>7</tpages></addata></record>
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subjects Acetates - analysis
Acetates - metabolism
adenocarcinoma
Adenocarcinoma - metabolism
Adenocarcinoma - pathology
benign prostatic hyperplasia
Biological and medical sciences
Citrates - analysis
Citrates - metabolism
Glutamates - analysis
Glutamates - metabolism
Humans
Hydrogen
Inositol - analysis
Inositol - metabolism
Investigative techniques, diagnostic techniques (general aspects)
Lactates - analysis
Lactates - metabolism
Magnetic Resonance Spectroscopy
Male
Medical sciences
N-Acetylneuraminic Acid
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
prostate
Prostate - chemistry
Prostate - metabolism
Prostate - pathology
Prostatic Hyperplasia - metabolism
Prostatic Hyperplasia - pathology
Prostatic Neoplasms - metabolism
Prostatic Neoplasms - pathology
Sialic Acids - analysis
Sialic Acids - metabolism
spectroscopy
Urinary system
title In vitro high resolution 1h-spectroscopy of the human prostate: Benign prostatic hyperplasia, normal peripheral zone and adenocarcinoma
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