Clinical distinction between Lewy bodies disease (LBD) and frontotemporal dementia (FTD) is sometimes difficult. Nigrostriatal dopaminergic degeneration occurs in both LBD and FTD, limiting helpfulness of DAT imaging to differentiate these forms of dementia. Several studies have emphasized the usefulness of myocardial scintigraphy with (123)Metaiodobenzylguanidine (I-123-MIGB) in assessing the sympathetic nerve terminals in LBD demonstrating that cardiac I-123-MIGB uptake is decreased in patients with this disease. We investigated the role of cardiac I-123-MIBG scintigraphy in differentiating patients with LBD from those with FTD. Clinical diagnosis of LBD and FTD was determined according to established consensus criteria. Nine patients with LBD (1 possible and 8 probable), 6 patients with FTD, and 16 control subjects were involved in the study. The heart to mediastinum ratio (H/M) of I-123-MIBG uptake was markedly reduced in all patients with LBD (HIM early: 1.25 +/- 0.12; delayed: 1.14 +/- 0.13) whereas it was normal in patients with FTD (H/M early: 1.86 +/- 0.20; delayed: 1.80 +/- 0.23) and in controls (H/M early: 1.91 +/- 0.17: delayed: 1.99 +/- 0.19), suggesting that cardiac I-123-MIBG scintigraphy can help distinguish patients with LBD from those with FTD. (C) 2008 Elsevier Inc. All rights reserved.
Clinical distinction between Lewy bodies disease (LBD) and frontotemporal dementia (FTD) is sometimes difficult. Nigrostriatal dopaminergic degeneration occurs in both LBD and FTD, limiting helpfulness of DAT imaging to differentiate these forms of dementia. Several studies have emphasized the usefulness of myocardial scintigraphy with (123)Metaiodobenzylguanidine (I-123-MIGB) in assessing the sympathetic nerve terminals in LBD demonstrating that cardiac I-123-MIGB uptake is decreased in patients with this disease. We investigated the role of cardiac I-123-MIBG scintigraphy in differentiating patients with LBD from those with FTD. Clinical diagnosis of LBD and FTD was determined according to established consensus criteria. Nine patients with LBD (1 possible and 8 probable), 6 patients with FTD, and 16 control subjects were involved in the study. The heart to mediastinum ratio (H/M) of I-123-MIBG uptake was markedly reduced in all patients with LBD (HIM early: 1.25 +/- 0.12; delayed: 1.14 +/- 0.13) whereas it was normal in patients with FTD (H/M early: 1.86 +/- 0.20; delayed: 1.80 +/- 0.23) and in controls (H/M early: 1.91 +/- 0.17: delayed: 1.99 +/- 0.19), suggesting that cardiac I-123-MIBG scintigraphy can help distinguish patients with LBD from those with FTD. (C) 2008 Elsevier Inc. All rights reserved.
Myocardial I-123-MIBG scintigraphy for differentiation of Lewy bodies disease from FTD
Arabia G;Cascini GL;Morelli M
2010-01-01
Abstract
Clinical distinction between Lewy bodies disease (LBD) and frontotemporal dementia (FTD) is sometimes difficult. Nigrostriatal dopaminergic degeneration occurs in both LBD and FTD, limiting helpfulness of DAT imaging to differentiate these forms of dementia. Several studies have emphasized the usefulness of myocardial scintigraphy with (123)Metaiodobenzylguanidine (I-123-MIGB) in assessing the sympathetic nerve terminals in LBD demonstrating that cardiac I-123-MIGB uptake is decreased in patients with this disease. We investigated the role of cardiac I-123-MIBG scintigraphy in differentiating patients with LBD from those with FTD. Clinical diagnosis of LBD and FTD was determined according to established consensus criteria. Nine patients with LBD (1 possible and 8 probable), 6 patients with FTD, and 16 control subjects were involved in the study. The heart to mediastinum ratio (H/M) of I-123-MIBG uptake was markedly reduced in all patients with LBD (HIM early: 1.25 +/- 0.12; delayed: 1.14 +/- 0.13) whereas it was normal in patients with FTD (H/M early: 1.86 +/- 0.20; delayed: 1.80 +/- 0.23) and in controls (H/M early: 1.91 +/- 0.17: delayed: 1.99 +/- 0.19), suggesting that cardiac I-123-MIBG scintigraphy can help distinguish patients with LBD from those with FTD. (C) 2008 Elsevier Inc. All rights reserved.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
