2017
DOI: 10.1016/j.jcmg.2016.06.005
|View full text |Cite
|
Sign up to set email alerts
|

Observations With Simultaneous 18F-FDG PET and MR Imaging in Peripheral Artery Disease

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
6
0

Year Published

2017
2017
2024
2024

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 7 publications
(7 citation statements)
references
References 4 publications
1
6
0
Order By: Relevance
“…Simultaneous acquisition of PET, when added to established imaging modalities, may thereby offer valuable complementary information to improve the assessment of atherosclerotic plaque composition in carotid, coronary, and peripheral artery disease (5,29,30). However, as previously reported, we observed no correlation of 18-FDG PET tracer uptake with cellular inflammation in SFA plaques (31), but we noted a trend toward increased uptake in fibroatheromas as compared to fibro-calcific plaques as identified by OCT. Other PET tracers might offer better characterization of LEAD plaques, but they were not available for human application at the time of initiation of our study. Gallium-68 DOTA-0-Tyr3-Octreotate (68Ga-DOTATATE) PET has shown potential in identifying vulnerable atherosclerotic plaques with high somatostatin receptor expression, while 11-carbon (11C)-choline and 18Ffluoromethylcholine (FMCH) tracers may improve the characterization of high-risk atherosclerotic plaques by detecting increased choline metabolism (32).…”
Section: Discussionsupporting
confidence: 59%
“…Simultaneous acquisition of PET, when added to established imaging modalities, may thereby offer valuable complementary information to improve the assessment of atherosclerotic plaque composition in carotid, coronary, and peripheral artery disease (5,29,30). However, as previously reported, we observed no correlation of 18-FDG PET tracer uptake with cellular inflammation in SFA plaques (31), but we noted a trend toward increased uptake in fibroatheromas as compared to fibro-calcific plaques as identified by OCT. Other PET tracers might offer better characterization of LEAD plaques, but they were not available for human application at the time of initiation of our study. Gallium-68 DOTA-0-Tyr3-Octreotate (68Ga-DOTATATE) PET has shown potential in identifying vulnerable atherosclerotic plaques with high somatostatin receptor expression, while 11-carbon (11C)-choline and 18Ffluoromethylcholine (FMCH) tracers may improve the characterization of high-risk atherosclerotic plaques by detecting increased choline metabolism (32).…”
Section: Discussionsupporting
confidence: 59%
“…Collectively, nuclear imaging techniques advance the non-invasive evaluation of PAD beyond traditional means by offering quantitative regional analysis of vascular and muscle physiology, whereas traditional non-invasive vascular diagnostic tools have primarily focused on hemodynamic (e.g., ABI, TBI, ultrasound) or structural (e.g., angiography) assessments of the lower extremities. It's important to note that while SPECT/CT and PET/CT imaging have demonstrated potential in PAD, the recent emergence of PET/MR imaging may also provide additional opportunities for partnering high-sensitivity molecular (PET) and high-resolution structural (MR) imaging in the setting of lower extremity PAD ( 38 , 48 ).…”
Section: Discussionmentioning
confidence: 99%
“…One recent study by Jiang et al ( 37 ) applied serial 18 F-FDG PET/CT imaging in PAD patients before and after sonodynamic therapy to the femoropopliteal artery, which demonstrated that PET/CT imaging could detect and quantify therapeutic reductions in arterial inflammation in the setting of PAD. Another recent study focused on evaluating the utility of a combined 18 F-FDG PET and MR imaging approach for simultaneous assessment of both plaque morphology and arterial inflammation in a small sample size of PAD patients, but did not find any significant correlations between 18 F-FDG arterial uptake and histological measures of arterial inflammation ( 38 ). Thus, ongoing work focused on targeted imaging of arterial inflammation in the setting of PAD is warranted to fully elucidate the potential role of PET imaging as a non-invasive biomarker of PAD-induced inflammation.…”
Section: Molecular Imaging Of Peripheral Artery Inflammation and Atherosclerosismentioning
confidence: 99%
“…In terms of molecular markers, there is a need to identify and validate novel markers that are specific and sensitive to PAD pathophysiology. Unlike carotid and coronary plaques, previous studies found that femoral artery plaque 18 F-FDG uptake did not correlate with plaque macrophage content and activity, suggesting a unique pathophysiology of PAD and a need for specific markers [ 116 , 146 ]. However, translating molecular markers from preclinical studies to clinical settings presents its challenges.…”
Section: Challenges and Future Directionsmentioning
confidence: 99%