Visualization of multiple organ amyloid involvement in systemic amyloidosis using 11C-PiB PET imaging
Purpose To investigate the utility of Pittsburgh compound B (PiB) positron emission tomography (PET) imaging for evaluating whole-body amyloid involvement in patients with systemic amyloidosis. Methods Whole-body 11 C-PiB PET was performed in seven patients with systemic immunoglobulin light-chain (...
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creator | Ezawa, Naoki Katoh, Nagaaki Oguchi, Kazuhiro Yoshinaga, Tsuneaki Yazaki, Masahide Sekijima, Yoshiki |
description | Purpose
To investigate the utility of Pittsburgh compound B (PiB) positron emission tomography (PET) imaging for evaluating whole-body amyloid involvement in patients with systemic amyloidosis.
Methods
Whole-body
11
C-PiB PET was performed in seven patients with systemic immunoglobulin light-chain (AL) amyloidosis, seven patients with hereditary transthyretin (ATTRm) amyloidosis, one asymptomatic
TTR
mutation carrier and three healthy controls. The correlations between clinical organ involvement, radiological
11
C-PiB uptake and histopathological findings were analysed for each organ.
Results
Organ involvement on
11
C-PiB PET imaging showed good correlations with the clinical findings for the heart and stomach. Abnormal tracer uptake was also observed in the spleen, lachrymal gland, submandibular gland, sublingual gland, lymph node, brain, scalp, extraocular muscles, nasal mucosa, pharynx, tongue and nuchal muscles, most of which were asymptomatic. Physiological tracer uptake was universally observed in the urinary tract (kidney, renal pelvis, ureter and bladder) and enterohepatic circulatory system (liver, gallbladder, bile duct and small intestine) in all participants. Most of the patients and one healthy control subject showed asymptomatic tracer uptake in the lung and parotid gland. The peripheral nervous system did not show any tracer uptake even in patients with apparent peripheral neuropathy. Histological amyloid deposition was confirmed in biopsied myocardium and gastric mucosa where abnormal
11
C-PiB retention was observed.
Conclusions
11
C-PiB PET imaging can be used clinically in the systemic evaluation of amyloid distribution in patients with AL and ATTRm amyloidosis. Quantitative analysis of
11
C-PiB PET images may be useful in therapy evaluation and will reveal whether amyloid clearance is correlated with clinical response. |
doi_str_mv | 10.1007/s00259-017-3814-1 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1937764205</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1993474973</sourcerecordid><originalsourceid>FETCH-LOGICAL-c388t-24d5569a67f948a229090de522e97be7a220f21593c5356baf848c27c53a17383</originalsourceid><addsrcrecordid>eNp1kMtKAzEUhgdRsFYfwF3AjZtoLpNJstRSL1Cwi-o2pNNMSckkNZkp1Kc3ZVREcHVu33845y-KS4xuMEL8NiFEmIQIc0gFLiE-Kka4whJyJOTxT87RaXGW0gYhLIiQo8K82dRrZz90Z4MHoQFt7zq7dQaEuNYe6Hbvgl0B63fB7UxrfJdzkPapM62tv-ch2QT6ZP0aYDyBc3sP5tMFsK1e5955cdJol8zFVxwXrw_TxeQJzl4enyd3M1hTITpIyhVjldQVb2QpNCESSbQyjBAj-dLw3EENwUzSmlFWLXUjSlETniuNORV0XFwPe7cxvPcmdaq1qTbOaW9CnxSWlPOqJIhl9OoPugl99Pm6TEla8lJymik8UHUMKUXTqG3MP8W9wkgdjFeD8Sobrw7GK5w1ZNCkzPq1ib82_yv6BHZbhNY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1993474973</pqid></control><display><type>article</type><title>Visualization of multiple organ amyloid involvement in systemic amyloidosis using 11C-PiB PET imaging</title><source>SpringerNature Journals</source><creator>Ezawa, Naoki ; Katoh, Nagaaki ; Oguchi, Kazuhiro ; Yoshinaga, Tsuneaki ; Yazaki, Masahide ; Sekijima, Yoshiki</creator><creatorcontrib>Ezawa, Naoki ; Katoh, Nagaaki ; Oguchi, Kazuhiro ; Yoshinaga, Tsuneaki ; Yazaki, Masahide ; Sekijima, Yoshiki</creatorcontrib><description>Purpose
To investigate the utility of Pittsburgh compound B (PiB) positron emission tomography (PET) imaging for evaluating whole-body amyloid involvement in patients with systemic amyloidosis.
Methods
Whole-body
11
C-PiB PET was performed in seven patients with systemic immunoglobulin light-chain (AL) amyloidosis, seven patients with hereditary transthyretin (ATTRm) amyloidosis, one asymptomatic
TTR
mutation carrier and three healthy controls. The correlations between clinical organ involvement, radiological
11
C-PiB uptake and histopathological findings were analysed for each organ.
Results
Organ involvement on
11
C-PiB PET imaging showed good correlations with the clinical findings for the heart and stomach. Abnormal tracer uptake was also observed in the spleen, lachrymal gland, submandibular gland, sublingual gland, lymph node, brain, scalp, extraocular muscles, nasal mucosa, pharynx, tongue and nuchal muscles, most of which were asymptomatic. Physiological tracer uptake was universally observed in the urinary tract (kidney, renal pelvis, ureter and bladder) and enterohepatic circulatory system (liver, gallbladder, bile duct and small intestine) in all participants. Most of the patients and one healthy control subject showed asymptomatic tracer uptake in the lung and parotid gland. The peripheral nervous system did not show any tracer uptake even in patients with apparent peripheral neuropathy. Histological amyloid deposition was confirmed in biopsied myocardium and gastric mucosa where abnormal
11
C-PiB retention was observed.
Conclusions
11
C-PiB PET imaging can be used clinically in the systemic evaluation of amyloid distribution in patients with AL and ATTRm amyloidosis. Quantitative analysis of
11
C-PiB PET images may be useful in therapy evaluation and will reveal whether amyloid clearance is correlated with clinical response.</description><identifier>ISSN: 1619-7070</identifier><identifier>EISSN: 1619-7089</identifier><identifier>DOI: 10.1007/s00259-017-3814-1</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Amyloidosis ; Bile ducts ; Bladder ; Brain ; Cardiology ; Circulatory system ; Correlation ; Emission analysis ; Evaluation ; Gallbladder ; Gastric mucosa ; Imaging ; Kidneys ; Liver ; Lungs ; Lymph nodes ; Medical imaging ; Medicine ; Medicine & Public Health ; Muscles ; Myocardium ; Nervous system ; Neuroimaging ; Nuclear Medicine ; Oculomotor system ; Oncology ; Original Article ; Orthopedics ; Patients ; Pelvis ; Peripheral nervous system ; Peripheral neuropathy ; Pharynx ; Positron emission ; Positron emission tomography ; Quantitative analysis ; Radiology ; Small intestine ; Spleen ; Stomach ; Tomography ; Tongue ; Urinary bladder ; Urinary tract</subject><ispartof>European journal of nuclear medicine and molecular imaging, 2018-03, Vol.45 (3), p.452-461</ispartof><rights>Springer-Verlag GmbH Germany 2017</rights><rights>European Journal of Nuclear Medicine and Molecular Imaging is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c388t-24d5569a67f948a229090de522e97be7a220f21593c5356baf848c27c53a17383</citedby><cites>FETCH-LOGICAL-c388t-24d5569a67f948a229090de522e97be7a220f21593c5356baf848c27c53a17383</cites><orcidid>0000-0002-6993-0607</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00259-017-3814-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00259-017-3814-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Ezawa, Naoki</creatorcontrib><creatorcontrib>Katoh, Nagaaki</creatorcontrib><creatorcontrib>Oguchi, Kazuhiro</creatorcontrib><creatorcontrib>Yoshinaga, Tsuneaki</creatorcontrib><creatorcontrib>Yazaki, Masahide</creatorcontrib><creatorcontrib>Sekijima, Yoshiki</creatorcontrib><title>Visualization of multiple organ amyloid involvement in systemic amyloidosis using 11C-PiB PET imaging</title><title>European journal of nuclear medicine and molecular imaging</title><addtitle>Eur J Nucl Med Mol Imaging</addtitle><description>Purpose
To investigate the utility of Pittsburgh compound B (PiB) positron emission tomography (PET) imaging for evaluating whole-body amyloid involvement in patients with systemic amyloidosis.
Methods
Whole-body
11
C-PiB PET was performed in seven patients with systemic immunoglobulin light-chain (AL) amyloidosis, seven patients with hereditary transthyretin (ATTRm) amyloidosis, one asymptomatic
TTR
mutation carrier and three healthy controls. The correlations between clinical organ involvement, radiological
11
C-PiB uptake and histopathological findings were analysed for each organ.
Results
Organ involvement on
11
C-PiB PET imaging showed good correlations with the clinical findings for the heart and stomach. Abnormal tracer uptake was also observed in the spleen, lachrymal gland, submandibular gland, sublingual gland, lymph node, brain, scalp, extraocular muscles, nasal mucosa, pharynx, tongue and nuchal muscles, most of which were asymptomatic. Physiological tracer uptake was universally observed in the urinary tract (kidney, renal pelvis, ureter and bladder) and enterohepatic circulatory system (liver, gallbladder, bile duct and small intestine) in all participants. Most of the patients and one healthy control subject showed asymptomatic tracer uptake in the lung and parotid gland. The peripheral nervous system did not show any tracer uptake even in patients with apparent peripheral neuropathy. Histological amyloid deposition was confirmed in biopsied myocardium and gastric mucosa where abnormal
11
C-PiB retention was observed.
Conclusions
11
C-PiB PET imaging can be used clinically in the systemic evaluation of amyloid distribution in patients with AL and ATTRm amyloidosis. Quantitative analysis of
11
C-PiB PET images may be useful in therapy evaluation and will reveal whether amyloid clearance is correlated with clinical response.</description><subject>Amyloidosis</subject><subject>Bile ducts</subject><subject>Bladder</subject><subject>Brain</subject><subject>Cardiology</subject><subject>Circulatory system</subject><subject>Correlation</subject><subject>Emission analysis</subject><subject>Evaluation</subject><subject>Gallbladder</subject><subject>Gastric mucosa</subject><subject>Imaging</subject><subject>Kidneys</subject><subject>Liver</subject><subject>Lungs</subject><subject>Lymph nodes</subject><subject>Medical imaging</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Muscles</subject><subject>Myocardium</subject><subject>Nervous system</subject><subject>Neuroimaging</subject><subject>Nuclear Medicine</subject><subject>Oculomotor system</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Patients</subject><subject>Pelvis</subject><subject>Peripheral nervous system</subject><subject>Peripheral neuropathy</subject><subject>Pharynx</subject><subject>Positron emission</subject><subject>Positron emission tomography</subject><subject>Quantitative analysis</subject><subject>Radiology</subject><subject>Small intestine</subject><subject>Spleen</subject><subject>Stomach</subject><subject>Tomography</subject><subject>Tongue</subject><subject>Urinary bladder</subject><subject>Urinary tract</subject><issn>1619-7070</issn><issn>1619-7089</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kMtKAzEUhgdRsFYfwF3AjZtoLpNJstRSL1Cwi-o2pNNMSckkNZkp1Kc3ZVREcHVu33845y-KS4xuMEL8NiFEmIQIc0gFLiE-Kka4whJyJOTxT87RaXGW0gYhLIiQo8K82dRrZz90Z4MHoQFt7zq7dQaEuNYe6Hbvgl0B63fB7UxrfJdzkPapM62tv-ch2QT6ZP0aYDyBc3sP5tMFsK1e5955cdJol8zFVxwXrw_TxeQJzl4enyd3M1hTITpIyhVjldQVb2QpNCESSbQyjBAj-dLw3EENwUzSmlFWLXUjSlETniuNORV0XFwPe7cxvPcmdaq1qTbOaW9CnxSWlPOqJIhl9OoPugl99Pm6TEla8lJymik8UHUMKUXTqG3MP8W9wkgdjFeD8Sobrw7GK5w1ZNCkzPq1ib82_yv6BHZbhNY</recordid><startdate>20180301</startdate><enddate>20180301</enddate><creator>Ezawa, Naoki</creator><creator>Katoh, Nagaaki</creator><creator>Oguchi, Kazuhiro</creator><creator>Yoshinaga, Tsuneaki</creator><creator>Yazaki, Masahide</creator><creator>Sekijima, Yoshiki</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</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>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>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6993-0607</orcidid></search><sort><creationdate>20180301</creationdate><title>Visualization of multiple organ amyloid involvement in systemic amyloidosis using 11C-PiB PET imaging</title><author>Ezawa, Naoki ; Katoh, Nagaaki ; Oguchi, Kazuhiro ; Yoshinaga, Tsuneaki ; Yazaki, Masahide ; Sekijima, Yoshiki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c388t-24d5569a67f948a229090de522e97be7a220f21593c5356baf848c27c53a17383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Amyloidosis</topic><topic>Bile ducts</topic><topic>Bladder</topic><topic>Brain</topic><topic>Cardiology</topic><topic>Circulatory system</topic><topic>Correlation</topic><topic>Emission analysis</topic><topic>Evaluation</topic><topic>Gallbladder</topic><topic>Gastric mucosa</topic><topic>Imaging</topic><topic>Kidneys</topic><topic>Liver</topic><topic>Lungs</topic><topic>Lymph nodes</topic><topic>Medical imaging</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Muscles</topic><topic>Myocardium</topic><topic>Nervous system</topic><topic>Neuroimaging</topic><topic>Nuclear Medicine</topic><topic>Oculomotor system</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Orthopedics</topic><topic>Patients</topic><topic>Pelvis</topic><topic>Peripheral nervous system</topic><topic>Peripheral neuropathy</topic><topic>Pharynx</topic><topic>Positron emission</topic><topic>Positron emission tomography</topic><topic>Quantitative analysis</topic><topic>Radiology</topic><topic>Small intestine</topic><topic>Spleen</topic><topic>Stomach</topic><topic>Tomography</topic><topic>Tongue</topic><topic>Urinary bladder</topic><topic>Urinary tract</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ezawa, Naoki</creatorcontrib><creatorcontrib>Katoh, Nagaaki</creatorcontrib><creatorcontrib>Oguchi, Kazuhiro</creatorcontrib><creatorcontrib>Yoshinaga, 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involvement in systemic amyloidosis using 11C-PiB PET imaging</atitle><jtitle>European journal of nuclear medicine and molecular imaging</jtitle><stitle>Eur J Nucl Med Mol Imaging</stitle><date>2018-03-01</date><risdate>2018</risdate><volume>45</volume><issue>3</issue><spage>452</spage><epage>461</epage><pages>452-461</pages><issn>1619-7070</issn><eissn>1619-7089</eissn><abstract>Purpose
To investigate the utility of Pittsburgh compound B (PiB) positron emission tomography (PET) imaging for evaluating whole-body amyloid involvement in patients with systemic amyloidosis.
Methods
Whole-body
11
C-PiB PET was performed in seven patients with systemic immunoglobulin light-chain (AL) amyloidosis, seven patients with hereditary transthyretin (ATTRm) amyloidosis, one asymptomatic
TTR
mutation carrier and three healthy controls. The correlations between clinical organ involvement, radiological
11
C-PiB uptake and histopathological findings were analysed for each organ.
Results
Organ involvement on
11
C-PiB PET imaging showed good correlations with the clinical findings for the heart and stomach. Abnormal tracer uptake was also observed in the spleen, lachrymal gland, submandibular gland, sublingual gland, lymph node, brain, scalp, extraocular muscles, nasal mucosa, pharynx, tongue and nuchal muscles, most of which were asymptomatic. Physiological tracer uptake was universally observed in the urinary tract (kidney, renal pelvis, ureter and bladder) and enterohepatic circulatory system (liver, gallbladder, bile duct and small intestine) in all participants. Most of the patients and one healthy control subject showed asymptomatic tracer uptake in the lung and parotid gland. The peripheral nervous system did not show any tracer uptake even in patients with apparent peripheral neuropathy. Histological amyloid deposition was confirmed in biopsied myocardium and gastric mucosa where abnormal
11
C-PiB retention was observed.
Conclusions
11
C-PiB PET imaging can be used clinically in the systemic evaluation of amyloid distribution in patients with AL and ATTRm amyloidosis. Quantitative analysis of
11
C-PiB PET images may be useful in therapy evaluation and will reveal whether amyloid clearance is correlated with clinical response.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s00259-017-3814-1</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-6993-0607</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amyloidosis Bile ducts Bladder Brain Cardiology Circulatory system Correlation Emission analysis Evaluation Gallbladder Gastric mucosa Imaging Kidneys Liver Lungs Lymph nodes Medical imaging Medicine Medicine & Public Health Muscles Myocardium Nervous system Neuroimaging Nuclear Medicine Oculomotor system Oncology Original Article Orthopedics Patients Pelvis Peripheral nervous system Peripheral neuropathy Pharynx Positron emission Positron emission tomography Quantitative analysis Radiology Small intestine Spleen Stomach Tomography Tongue Urinary bladder Urinary tract |
title | Visualization of multiple organ amyloid involvement in systemic amyloidosis using 11C-PiB PET imaging |
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