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Initial clinical experience with oral manganese (CMC-001) for liver MR imaging
Recently, a new oral liver-specific manganese-based MR agent (CMC-001) has been introduced. This contrast medium is delivered to the liver in high concentrations in the portal vein and very low doses in the hepatic artery, as only small amounts of manganese enter the general circulation. It is taken...
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Published in: | European radiology 2007-01, Vol.17 (1), p.273-278 |
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creator | Thomsen, Henrik S Barentsz, Jelle O Burcharth, Flemming Chabanova, Elizaveta Dekker, Helena M Moesgaard, Flemming Moller, Jakob M Leth-Espensen, Per Logager, Vibeke Takahashi, Satoru |
description | Recently, a new oral liver-specific manganese-based MR agent (CMC-001) has been introduced. This contrast medium is delivered to the liver in high concentrations in the portal vein and very low doses in the hepatic artery, as only small amounts of manganese enter the general circulation. It is taken up by the hepatocytes and excreted in the bile. Our initial experience with the new MR contrast medium in a variety of patients is reported. A total of 20 patients (11 males and 9 females) were studied with MR imaging 2 h after oral ingestion of the contrast agent. Sixteen patients were referred for evaluation of focal liver lesion(s), whereas in the remaining four patients, evaluation of the biliary tract was requested. In the 17 patients without biliary obstruction, there was an increased signal intensity of the liver parenchyma, whereas in the three patients with biliary obstruction, the uptake was delayed. There was excellent visualization of the biliary system on the T1-weighted images in the 16 patients without biliary obstruction referred for evaluation of a focal liver lesion. In seven patients, the uptake was patchy. In patients with focal liver lesions or biliary tract diseases, it is possible to increase the signal intensity of the liver parenchyma after the oral intake of CMC-001. In patients without biliary tract obstruction, the biliary system is easily visualized. Oral manganese seems to be useful in hepatobiliary MRI. Further research is strongly warranted. |
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This contrast medium is delivered to the liver in high concentrations in the portal vein and very low doses in the hepatic artery, as only small amounts of manganese enter the general circulation. It is taken up by the hepatocytes and excreted in the bile. Our initial experience with the new MR contrast medium in a variety of patients is reported. A total of 20 patients (11 males and 9 females) were studied with MR imaging 2 h after oral ingestion of the contrast agent. Sixteen patients were referred for evaluation of focal liver lesion(s), whereas in the remaining four patients, evaluation of the biliary tract was requested. In the 17 patients without biliary obstruction, there was an increased signal intensity of the liver parenchyma, whereas in the three patients with biliary obstruction, the uptake was delayed. There was excellent visualization of the biliary system on the T1-weighted images in the 16 patients without biliary obstruction referred for evaluation of a focal liver lesion. In seven patients, the uptake was patchy. In patients with focal liver lesions or biliary tract diseases, it is possible to increase the signal intensity of the liver parenchyma after the oral intake of CMC-001. In patients without biliary tract obstruction, the biliary system is easily visualized. Oral manganese seems to be useful in hepatobiliary MRI. Further research is strongly warranted.</description><identifier>ISSN: 0938-7994</identifier><identifier>EISSN: 1432-1084</identifier><identifier>DOI: 10.1007/s00330-006-0336-9</identifier><identifier>PMID: 16763790</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Adult ; Aged ; Biliary tract ; Biliary tract diseases ; Contrast agents ; Contrast media ; Contrast Media - administration & dosage ; Female ; Hepatic artery ; Hepatocytes ; Humans ; Ingestion ; Lesions ; Liver ; Liver diseases ; Liver Diseases - diagnosis ; Magnetic Resonance Imaging ; Male ; Manganese ; Manganese - administration & dosage ; Medical imaging ; Middle Aged ; Parenchyma ; Portal vein ; Retrospective Studies</subject><ispartof>European radiology, 2007-01, Vol.17 (1), p.273-278</ispartof><rights>Springer-Verlag 2006.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c327t-af3af29efa1fd45f196362d9925e53624588ce1a3dfee7addf5f015237ad71f03</citedby><cites>FETCH-LOGICAL-c327t-af3af29efa1fd45f196362d9925e53624588ce1a3dfee7addf5f015237ad71f03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16763790$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thomsen, Henrik S</creatorcontrib><creatorcontrib>Barentsz, Jelle O</creatorcontrib><creatorcontrib>Burcharth, Flemming</creatorcontrib><creatorcontrib>Chabanova, Elizaveta</creatorcontrib><creatorcontrib>Dekker, Helena M</creatorcontrib><creatorcontrib>Moesgaard, Flemming</creatorcontrib><creatorcontrib>Moller, Jakob M</creatorcontrib><creatorcontrib>Leth-Espensen, Per</creatorcontrib><creatorcontrib>Logager, Vibeke</creatorcontrib><creatorcontrib>Takahashi, Satoru</creatorcontrib><title>Initial clinical experience with oral manganese (CMC-001) for liver MR imaging</title><title>European radiology</title><addtitle>Eur Radiol</addtitle><description>Recently, a new oral liver-specific manganese-based MR agent (CMC-001) has been introduced. This contrast medium is delivered to the liver in high concentrations in the portal vein and very low doses in the hepatic artery, as only small amounts of manganese enter the general circulation. It is taken up by the hepatocytes and excreted in the bile. Our initial experience with the new MR contrast medium in a variety of patients is reported. A total of 20 patients (11 males and 9 females) were studied with MR imaging 2 h after oral ingestion of the contrast agent. Sixteen patients were referred for evaluation of focal liver lesion(s), whereas in the remaining four patients, evaluation of the biliary tract was requested. In the 17 patients without biliary obstruction, there was an increased signal intensity of the liver parenchyma, whereas in the three patients with biliary obstruction, the uptake was delayed. There was excellent visualization of the biliary system on the T1-weighted images in the 16 patients without biliary obstruction referred for evaluation of a focal liver lesion. In seven patients, the uptake was patchy. In patients with focal liver lesions or biliary tract diseases, it is possible to increase the signal intensity of the liver parenchyma after the oral intake of CMC-001. In patients without biliary tract obstruction, the biliary system is easily visualized. Oral manganese seems to be useful in hepatobiliary MRI. Further research is strongly warranted.</description><subject>Adult</subject><subject>Aged</subject><subject>Biliary tract</subject><subject>Biliary tract diseases</subject><subject>Contrast agents</subject><subject>Contrast media</subject><subject>Contrast Media - administration & dosage</subject><subject>Female</subject><subject>Hepatic artery</subject><subject>Hepatocytes</subject><subject>Humans</subject><subject>Ingestion</subject><subject>Lesions</subject><subject>Liver</subject><subject>Liver diseases</subject><subject>Liver Diseases - diagnosis</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Manganese</subject><subject>Manganese - administration & dosage</subject><subject>Medical imaging</subject><subject>Middle Aged</subject><subject>Parenchyma</subject><subject>Portal vein</subject><subject>Retrospective Studies</subject><issn>0938-7994</issn><issn>1432-1084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNpdkFtLxDAQhYMouq7-AF-kIIg-VGeaNGkeZfEGq4Loc4jtZI102zXZevn3RnZB8GkOw5mZMx9jBwhnCKDOIwDnkAPIPAmZ6w02QsGLHKESm2wEmle50lrssN0Y3wBAo1DbbAelklxpGLH7284vvW2zuvWdr5OgrwUFT11N2adfvmZ9SM257Wa2o0jZyeRuki7iaeb6kLX-g0J295j5uZ35brbHtpxtI-2v65g9X10-TW7y6cP17eRimte8UMvcOm5doclZdI0oHWrJZdFoXZRUJiXKqqoJLW8ckbJN40oHWBY8aYUO-Jgdr_YuQv8-UFyauY81tW0K2Q_RyEqAlkIm49E_41s_hC5lMxwLJQCVwuTClasOfYyBnFmE9FH4NgjmF7VZoTYJtflFbXSaOVxvHl7m1PxNrNnyH_iFd2Y</recordid><startdate>20070101</startdate><enddate>20070101</enddate><creator>Thomsen, Henrik S</creator><creator>Barentsz, Jelle O</creator><creator>Burcharth, Flemming</creator><creator>Chabanova, Elizaveta</creator><creator>Dekker, Helena M</creator><creator>Moesgaard, Flemming</creator><creator>Moller, Jakob M</creator><creator>Leth-Espensen, Per</creator><creator>Logager, Vibeke</creator><creator>Takahashi, Satoru</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QO</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20070101</creationdate><title>Initial clinical experience with oral manganese (CMC-001) for liver MR imaging</title><author>Thomsen, Henrik S ; Barentsz, Jelle O ; Burcharth, Flemming ; Chabanova, Elizaveta ; Dekker, Helena M ; Moesgaard, Flemming ; Moller, Jakob M ; Leth-Espensen, Per ; Logager, Vibeke ; Takahashi, Satoru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c327t-af3af29efa1fd45f196362d9925e53624588ce1a3dfee7addf5f015237ad71f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biliary tract</topic><topic>Biliary tract diseases</topic><topic>Contrast agents</topic><topic>Contrast media</topic><topic>Contrast Media - administration & dosage</topic><topic>Female</topic><topic>Hepatic artery</topic><topic>Hepatocytes</topic><topic>Humans</topic><topic>Ingestion</topic><topic>Lesions</topic><topic>Liver</topic><topic>Liver diseases</topic><topic>Liver Diseases - diagnosis</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Manganese</topic><topic>Manganese - administration & dosage</topic><topic>Medical imaging</topic><topic>Middle Aged</topic><topic>Parenchyma</topic><topic>Portal vein</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thomsen, Henrik S</creatorcontrib><creatorcontrib>Barentsz, Jelle O</creatorcontrib><creatorcontrib>Burcharth, Flemming</creatorcontrib><creatorcontrib>Chabanova, Elizaveta</creatorcontrib><creatorcontrib>Dekker, Helena M</creatorcontrib><creatorcontrib>Moesgaard, Flemming</creatorcontrib><creatorcontrib>Moller, Jakob M</creatorcontrib><creatorcontrib>Leth-Espensen, Per</creatorcontrib><creatorcontrib>Logager, Vibeke</creatorcontrib><creatorcontrib>Takahashi, Satoru</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</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>MEDLINE - Academic</collection><jtitle>European radiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thomsen, Henrik S</au><au>Barentsz, Jelle O</au><au>Burcharth, Flemming</au><au>Chabanova, Elizaveta</au><au>Dekker, Helena M</au><au>Moesgaard, Flemming</au><au>Moller, Jakob M</au><au>Leth-Espensen, Per</au><au>Logager, Vibeke</au><au>Takahashi, Satoru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Initial clinical experience with oral manganese (CMC-001) for liver MR imaging</atitle><jtitle>European radiology</jtitle><addtitle>Eur Radiol</addtitle><date>2007-01-01</date><risdate>2007</risdate><volume>17</volume><issue>1</issue><spage>273</spage><epage>278</epage><pages>273-278</pages><issn>0938-7994</issn><eissn>1432-1084</eissn><abstract>Recently, a new oral liver-specific manganese-based MR agent (CMC-001) has been introduced. This contrast medium is delivered to the liver in high concentrations in the portal vein and very low doses in the hepatic artery, as only small amounts of manganese enter the general circulation. It is taken up by the hepatocytes and excreted in the bile. Our initial experience with the new MR contrast medium in a variety of patients is reported. A total of 20 patients (11 males and 9 females) were studied with MR imaging 2 h after oral ingestion of the contrast agent. Sixteen patients were referred for evaluation of focal liver lesion(s), whereas in the remaining four patients, evaluation of the biliary tract was requested. In the 17 patients without biliary obstruction, there was an increased signal intensity of the liver parenchyma, whereas in the three patients with biliary obstruction, the uptake was delayed. There was excellent visualization of the biliary system on the T1-weighted images in the 16 patients without biliary obstruction referred for evaluation of a focal liver lesion. In seven patients, the uptake was patchy. In patients with focal liver lesions or biliary tract diseases, it is possible to increase the signal intensity of the liver parenchyma after the oral intake of CMC-001. In patients without biliary tract obstruction, the biliary system is easily visualized. Oral manganese seems to be useful in hepatobiliary MRI. Further research is strongly warranted.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>16763790</pmid><doi>10.1007/s00330-006-0336-9</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Aged Biliary tract Biliary tract diseases Contrast agents Contrast media Contrast Media - administration & dosage Female Hepatic artery Hepatocytes Humans Ingestion Lesions Liver Liver diseases Liver Diseases - diagnosis Magnetic Resonance Imaging Male Manganese Manganese - administration & dosage Medical imaging Middle Aged Parenchyma Portal vein Retrospective Studies |
title | Initial clinical experience with oral manganese (CMC-001) for liver MR imaging |
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