Simultaneous hyperpolarized 13C-pyruvate MRI and 18F-FDG-PET in cancer (hyperPET): feasibility of a new imaging concept using a clinical PET/MRI scanner
In this paper we demonstrate, for the first time, the feasibility of a new imaging concept - combined hyperpolarized 13 C-pyruvate magnetic resonance spectroscopic imaging (MRSI) and 18 F-FDG-PET imaging. This procedure was performed in a clinical PET/MRI scanner with a canine cancer patient. We hav...
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creator | Gutte, Henrik Hansen, Adam E Henriksen, Sarah T Johannesen, Helle H Ardenkjaer-Larsen, Jan Vignaud, Alexandre Hansen, Anders E Børresen, Betina Klausen, Thomas L Wittekind, Anne-Mette N Gillings, Nic Kristensen, Annemarie T Clemmensen, Andreas Højgaard, Liselotte Kjær, Andreas |
description | In this paper we demonstrate, for the first time, the feasibility of a new imaging concept - combined hyperpolarized
13
C-pyruvate magnetic resonance spectroscopic imaging (MRSI) and
18
F-FDG-PET imaging. This procedure was performed in a clinical PET/MRI scanner with a canine cancer patient. We have named this concept
hyper PET
. Intravenous injection of the hyperpolarized
13
C-pyruvate results in an increase of
13
C-lactate,
13
C-alanine and
13
C-CO
2
(
13
C-HCO
3
) resonance peaks relative to the tissue, disease and the metabolic state probed. Accordingly, with dynamic nuclear polarization (DNP) and use of
13
C-pyruvate it is now possible to directly study the
Warburg Effect
through the rate of conversion of
13
C-pyruvate to
13
C-lactate. In this study, we combined it with
18
F-FDG-PET that studies uptake of glucose in the cells. A canine cancer patient with a histology verified local recurrence of a liposarcoma on the right forepaw was imaged using a combined PET/MR clinical scanner. PET was performed as a single-bed, 10 min acquisition, 107 min post injection of 310 MBq
18
F-FDG.
13
C-chemical shift imaging (CSI) was performed just after FDG-PET and 30 s post injection of 23 mL hyperpolarized
13
C-pyruvate. Peak heights of
13
C-pyruvate and
13
C-lactate were quantified using a general linear model. Anatomic
1
H-MRI included axial and coronal T1 vibe, coronal T2-tse and axial T1-tse with fat saturation following gadolinium injection. In the tumor we found clearly increased
13
C-lactate production, which also corresponded to high
18
F-FDG uptake on PET. This is in agreement with the fact that glycolysis and production of lactate are increased in tumor cells compared to normal cells. Yet,
most interestingly
, also in the muscle of the forepaw of the dog high
18
F-FDG uptake was observed. This was due to activity in these muscles prior to anesthesia, which was
not
accompanied by a similarly high
13
C-lactate production. Accordingly, this clearly demonstrates how the
Warburg Effect
directly can be demonstrated by hyperpolarized
13
C-pyruvate MRSI. This was not possible with
18
F-FDG-PET imaging due to inability to discriminate between causes of increased glucose uptake. We propose that this new concept of simultaneous hyperpolarized
13
C-pyruvate MRSI and PET may be highly valuable for image-based non-invasive phenotyping of tumors. This methods may be useful for treatment planning and therapy monitoring. |
format | Article |
fullrecord | <record><control><sourceid>pubmedcentral</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4299777</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>pubmedcentral_primary_oai_pubmedcentral_nih_gov_4299777</sourcerecordid><originalsourceid>FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_42997773</originalsourceid><addsrcrecordid>eNqljTFPwzAQhS0kRCvof7gRhgg3bZKGgaU0lAEJQffo6l7SQ65t2UlR-CX8XFzEwswtT_fuve_OxDid5jJZzGUxEpMQ3mWcTMoyLy_EKM3yNJNpNhZfb3zodYeGbB9gPzjyzmr0_Ek7mM6WiRt8f8SO4Pn1CdBEc1El1cNj8rLaABtQaBR5uP6pRu_mDhrCwFvW3A1gG0Aw9AF8wJZNC8rGvOugD6cNQWk2rFBD7N6efoRINOSvxHmDOtDkVy_FfbXaLNeJ67cH2ikynUddOx_Bfqgtcv33Ynhft_ZYz9OyLIpi9m_AN7dVb3A</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Simultaneous hyperpolarized 13C-pyruvate MRI and 18F-FDG-PET in cancer (hyperPET): feasibility of a new imaging concept using a clinical PET/MRI scanner</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Gutte, Henrik ; Hansen, Adam E ; Henriksen, Sarah T ; Johannesen, Helle H ; Ardenkjaer-Larsen, Jan ; Vignaud, Alexandre ; Hansen, Anders E ; Børresen, Betina ; Klausen, Thomas L ; Wittekind, Anne-Mette N ; Gillings, Nic ; Kristensen, Annemarie T ; Clemmensen, Andreas ; Højgaard, Liselotte ; Kjær, Andreas</creator><creatorcontrib>Gutte, Henrik ; Hansen, Adam E ; Henriksen, Sarah T ; Johannesen, Helle H ; Ardenkjaer-Larsen, Jan ; Vignaud, Alexandre ; Hansen, Anders E ; Børresen, Betina ; Klausen, Thomas L ; Wittekind, Anne-Mette N ; Gillings, Nic ; Kristensen, Annemarie T ; Clemmensen, Andreas ; Højgaard, Liselotte ; Kjær, Andreas</creatorcontrib><description>In this paper we demonstrate, for the first time, the feasibility of a new imaging concept - combined hyperpolarized
13
C-pyruvate magnetic resonance spectroscopic imaging (MRSI) and
18
F-FDG-PET imaging. This procedure was performed in a clinical PET/MRI scanner with a canine cancer patient. We have named this concept
hyper PET
. Intravenous injection of the hyperpolarized
13
C-pyruvate results in an increase of
13
C-lactate,
13
C-alanine and
13
C-CO
2
(
13
C-HCO
3
) resonance peaks relative to the tissue, disease and the metabolic state probed. Accordingly, with dynamic nuclear polarization (DNP) and use of
13
C-pyruvate it is now possible to directly study the
Warburg Effect
through the rate of conversion of
13
C-pyruvate to
13
C-lactate. In this study, we combined it with
18
F-FDG-PET that studies uptake of glucose in the cells. A canine cancer patient with a histology verified local recurrence of a liposarcoma on the right forepaw was imaged using a combined PET/MR clinical scanner. PET was performed as a single-bed, 10 min acquisition, 107 min post injection of 310 MBq
18
F-FDG.
13
C-chemical shift imaging (CSI) was performed just after FDG-PET and 30 s post injection of 23 mL hyperpolarized
13
C-pyruvate. Peak heights of
13
C-pyruvate and
13
C-lactate were quantified using a general linear model. Anatomic
1
H-MRI included axial and coronal T1 vibe, coronal T2-tse and axial T1-tse with fat saturation following gadolinium injection. In the tumor we found clearly increased
13
C-lactate production, which also corresponded to high
18
F-FDG uptake on PET. This is in agreement with the fact that glycolysis and production of lactate are increased in tumor cells compared to normal cells. Yet,
most interestingly
, also in the muscle of the forepaw of the dog high
18
F-FDG uptake was observed. This was due to activity in these muscles prior to anesthesia, which was
not
accompanied by a similarly high
13
C-lactate production. Accordingly, this clearly demonstrates how the
Warburg Effect
directly can be demonstrated by hyperpolarized
13
C-pyruvate MRSI. This was not possible with
18
F-FDG-PET imaging due to inability to discriminate between causes of increased glucose uptake. We propose that this new concept of simultaneous hyperpolarized
13
C-pyruvate MRSI and PET may be highly valuable for image-based non-invasive phenotyping of tumors. This methods may be useful for treatment planning and therapy monitoring.</description><identifier>EISSN: 2160-8407</identifier><identifier>PMID: 25625025</identifier><language>eng</language><publisher>e-Century Publishing Corporation</publisher><subject>Original</subject><ispartof>American journal of nuclear medicine and molecular imaging, 2014-12, Vol.5 (1), p.38-45</ispartof><rights>AJNMMI Copyright © 2015 2015</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299777/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299777/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,725,778,782,883,53774,53776</link.rule.ids></links><search><creatorcontrib>Gutte, Henrik</creatorcontrib><creatorcontrib>Hansen, Adam E</creatorcontrib><creatorcontrib>Henriksen, Sarah T</creatorcontrib><creatorcontrib>Johannesen, Helle H</creatorcontrib><creatorcontrib>Ardenkjaer-Larsen, Jan</creatorcontrib><creatorcontrib>Vignaud, Alexandre</creatorcontrib><creatorcontrib>Hansen, Anders E</creatorcontrib><creatorcontrib>Børresen, Betina</creatorcontrib><creatorcontrib>Klausen, Thomas L</creatorcontrib><creatorcontrib>Wittekind, Anne-Mette N</creatorcontrib><creatorcontrib>Gillings, Nic</creatorcontrib><creatorcontrib>Kristensen, Annemarie T</creatorcontrib><creatorcontrib>Clemmensen, Andreas</creatorcontrib><creatorcontrib>Højgaard, Liselotte</creatorcontrib><creatorcontrib>Kjær, Andreas</creatorcontrib><title>Simultaneous hyperpolarized 13C-pyruvate MRI and 18F-FDG-PET in cancer (hyperPET): feasibility of a new imaging concept using a clinical PET/MRI scanner</title><title>American journal of nuclear medicine and molecular imaging</title><description>In this paper we demonstrate, for the first time, the feasibility of a new imaging concept - combined hyperpolarized
13
C-pyruvate magnetic resonance spectroscopic imaging (MRSI) and
18
F-FDG-PET imaging. This procedure was performed in a clinical PET/MRI scanner with a canine cancer patient. We have named this concept
hyper PET
. Intravenous injection of the hyperpolarized
13
C-pyruvate results in an increase of
13
C-lactate,
13
C-alanine and
13
C-CO
2
(
13
C-HCO
3
) resonance peaks relative to the tissue, disease and the metabolic state probed. Accordingly, with dynamic nuclear polarization (DNP) and use of
13
C-pyruvate it is now possible to directly study the
Warburg Effect
through the rate of conversion of
13
C-pyruvate to
13
C-lactate. In this study, we combined it with
18
F-FDG-PET that studies uptake of glucose in the cells. A canine cancer patient with a histology verified local recurrence of a liposarcoma on the right forepaw was imaged using a combined PET/MR clinical scanner. PET was performed as a single-bed, 10 min acquisition, 107 min post injection of 310 MBq
18
F-FDG.
13
C-chemical shift imaging (CSI) was performed just after FDG-PET and 30 s post injection of 23 mL hyperpolarized
13
C-pyruvate. Peak heights of
13
C-pyruvate and
13
C-lactate were quantified using a general linear model. Anatomic
1
H-MRI included axial and coronal T1 vibe, coronal T2-tse and axial T1-tse with fat saturation following gadolinium injection. In the tumor we found clearly increased
13
C-lactate production, which also corresponded to high
18
F-FDG uptake on PET. This is in agreement with the fact that glycolysis and production of lactate are increased in tumor cells compared to normal cells. Yet,
most interestingly
, also in the muscle of the forepaw of the dog high
18
F-FDG uptake was observed. This was due to activity in these muscles prior to anesthesia, which was
not
accompanied by a similarly high
13
C-lactate production. Accordingly, this clearly demonstrates how the
Warburg Effect
directly can be demonstrated by hyperpolarized
13
C-pyruvate MRSI. This was not possible with
18
F-FDG-PET imaging due to inability to discriminate between causes of increased glucose uptake. We propose that this new concept of simultaneous hyperpolarized
13
C-pyruvate MRSI and PET may be highly valuable for image-based non-invasive phenotyping of tumors. This methods may be useful for treatment planning and therapy monitoring.</description><subject>Original</subject><issn>2160-8407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqljTFPwzAQhS0kRCvof7gRhgg3bZKGgaU0lAEJQffo6l7SQ65t2UlR-CX8XFzEwswtT_fuve_OxDid5jJZzGUxEpMQ3mWcTMoyLy_EKM3yNJNpNhZfb3zodYeGbB9gPzjyzmr0_Ek7mM6WiRt8f8SO4Pn1CdBEc1El1cNj8rLaABtQaBR5uP6pRu_mDhrCwFvW3A1gG0Aw9AF8wJZNC8rGvOugD6cNQWk2rFBD7N6efoRINOSvxHmDOtDkVy_FfbXaLNeJ67cH2ikynUddOx_Bfqgtcv33Ynhft_ZYz9OyLIpi9m_AN7dVb3A</recordid><startdate>20141215</startdate><enddate>20141215</enddate><creator>Gutte, Henrik</creator><creator>Hansen, Adam E</creator><creator>Henriksen, Sarah T</creator><creator>Johannesen, Helle H</creator><creator>Ardenkjaer-Larsen, Jan</creator><creator>Vignaud, Alexandre</creator><creator>Hansen, Anders E</creator><creator>Børresen, Betina</creator><creator>Klausen, Thomas L</creator><creator>Wittekind, Anne-Mette N</creator><creator>Gillings, Nic</creator><creator>Kristensen, Annemarie T</creator><creator>Clemmensen, Andreas</creator><creator>Højgaard, Liselotte</creator><creator>Kjær, Andreas</creator><general>e-Century Publishing Corporation</general><scope>5PM</scope></search><sort><creationdate>20141215</creationdate><title>Simultaneous hyperpolarized 13C-pyruvate MRI and 18F-FDG-PET in cancer (hyperPET): feasibility of a new imaging concept using a clinical PET/MRI scanner</title><author>Gutte, Henrik ; Hansen, Adam E ; Henriksen, Sarah T ; Johannesen, Helle H ; Ardenkjaer-Larsen, Jan ; Vignaud, Alexandre ; Hansen, Anders E ; Børresen, Betina ; Klausen, Thomas L ; Wittekind, Anne-Mette N ; Gillings, Nic ; Kristensen, Annemarie T ; Clemmensen, Andreas ; Højgaard, Liselotte ; Kjær, Andreas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_42997773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Original</topic><toplevel>online_resources</toplevel><creatorcontrib>Gutte, Henrik</creatorcontrib><creatorcontrib>Hansen, Adam E</creatorcontrib><creatorcontrib>Henriksen, Sarah T</creatorcontrib><creatorcontrib>Johannesen, Helle H</creatorcontrib><creatorcontrib>Ardenkjaer-Larsen, Jan</creatorcontrib><creatorcontrib>Vignaud, Alexandre</creatorcontrib><creatorcontrib>Hansen, Anders E</creatorcontrib><creatorcontrib>Børresen, Betina</creatorcontrib><creatorcontrib>Klausen, Thomas L</creatorcontrib><creatorcontrib>Wittekind, Anne-Mette N</creatorcontrib><creatorcontrib>Gillings, Nic</creatorcontrib><creatorcontrib>Kristensen, Annemarie T</creatorcontrib><creatorcontrib>Clemmensen, Andreas</creatorcontrib><creatorcontrib>Højgaard, Liselotte</creatorcontrib><creatorcontrib>Kjær, Andreas</creatorcontrib><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of nuclear medicine and molecular imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gutte, Henrik</au><au>Hansen, Adam E</au><au>Henriksen, Sarah T</au><au>Johannesen, Helle H</au><au>Ardenkjaer-Larsen, Jan</au><au>Vignaud, Alexandre</au><au>Hansen, Anders E</au><au>Børresen, Betina</au><au>Klausen, Thomas L</au><au>Wittekind, Anne-Mette N</au><au>Gillings, Nic</au><au>Kristensen, Annemarie T</au><au>Clemmensen, Andreas</au><au>Højgaard, Liselotte</au><au>Kjær, Andreas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous hyperpolarized 13C-pyruvate MRI and 18F-FDG-PET in cancer (hyperPET): feasibility of a new imaging concept using a clinical PET/MRI scanner</atitle><jtitle>American journal of nuclear medicine and molecular imaging</jtitle><date>2014-12-15</date><risdate>2014</risdate><volume>5</volume><issue>1</issue><spage>38</spage><epage>45</epage><pages>38-45</pages><eissn>2160-8407</eissn><abstract>In this paper we demonstrate, for the first time, the feasibility of a new imaging concept - combined hyperpolarized
13
C-pyruvate magnetic resonance spectroscopic imaging (MRSI) and
18
F-FDG-PET imaging. This procedure was performed in a clinical PET/MRI scanner with a canine cancer patient. We have named this concept
hyper PET
. Intravenous injection of the hyperpolarized
13
C-pyruvate results in an increase of
13
C-lactate,
13
C-alanine and
13
C-CO
2
(
13
C-HCO
3
) resonance peaks relative to the tissue, disease and the metabolic state probed. Accordingly, with dynamic nuclear polarization (DNP) and use of
13
C-pyruvate it is now possible to directly study the
Warburg Effect
through the rate of conversion of
13
C-pyruvate to
13
C-lactate. In this study, we combined it with
18
F-FDG-PET that studies uptake of glucose in the cells. A canine cancer patient with a histology verified local recurrence of a liposarcoma on the right forepaw was imaged using a combined PET/MR clinical scanner. PET was performed as a single-bed, 10 min acquisition, 107 min post injection of 310 MBq
18
F-FDG.
13
C-chemical shift imaging (CSI) was performed just after FDG-PET and 30 s post injection of 23 mL hyperpolarized
13
C-pyruvate. Peak heights of
13
C-pyruvate and
13
C-lactate were quantified using a general linear model. Anatomic
1
H-MRI included axial and coronal T1 vibe, coronal T2-tse and axial T1-tse with fat saturation following gadolinium injection. In the tumor we found clearly increased
13
C-lactate production, which also corresponded to high
18
F-FDG uptake on PET. This is in agreement with the fact that glycolysis and production of lactate are increased in tumor cells compared to normal cells. Yet,
most interestingly
, also in the muscle of the forepaw of the dog high
18
F-FDG uptake was observed. This was due to activity in these muscles prior to anesthesia, which was
not
accompanied by a similarly high
13
C-lactate production. Accordingly, this clearly demonstrates how the
Warburg Effect
directly can be demonstrated by hyperpolarized
13
C-pyruvate MRSI. This was not possible with
18
F-FDG-PET imaging due to inability to discriminate between causes of increased glucose uptake. We propose that this new concept of simultaneous hyperpolarized
13
C-pyruvate MRSI and PET may be highly valuable for image-based non-invasive phenotyping of tumors. This methods may be useful for treatment planning and therapy monitoring.</abstract><pub>e-Century Publishing Corporation</pub><pmid>25625025</pmid></addata></record> |
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title | Simultaneous hyperpolarized 13C-pyruvate MRI and 18F-FDG-PET in cancer (hyperPET): feasibility of a new imaging concept using a clinical PET/MRI scanner |
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