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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Veröffentlicht in:European journal of nuclear medicine and molecular imaging 2018-03, Vol.45 (3), p.452-461
Hauptverfasser: Ezawa, Naoki, Katoh, Nagaaki, Oguchi, Kazuhiro, Yoshinaga, Tsuneaki, Yazaki, Masahide, Sekijima, Yoshiki
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container_title European journal of nuclear medicine and molecular imaging
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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
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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 &amp; 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 &amp; 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 ; 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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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