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High-dose contrast-enhanced MRI in multiple sclerosis
T Koudriavtseva1, C Pozzilli, C Di Biasi
1Department of Neurosciences, University of Rome, La Sapienza, Italy.
Abstract:
Contrast-enhanced MRI is effective for assessing disease activity in multiple sclerosis (MS) and may provide an outcome measure for testing the efficacy of treatment in clinical trials. To compare the sensitivity of high-dose gadolinium-HP-DO3A with that of a standard dose of gadolinium-DTPA, we studied 16 patients with relapsing-remitting MS in the acute phase of the disease. Each underwent two MRI examinations within at most 48 h. The initial MRI study was with a standard dose of gadolinium-DTPA (0.1 mmol/kg), and the second one an experimental dose of gadolinium-HP-DO3A (0.3 mmol/kg). No adverse effects were attributed to the contrast media. The high-dose study revealed more enhancing lesions than the standard-dose study (56 vs 38). This difference was found to be more relevant for infratentorial and small lesions. Furthermore, with the higher dose, there was a marked qualitative improvement in the visibility and delineation of the lesions.
Insights
High-dose gadolinium-HP-DO3A contrast agent detected more active lesions in multiple sclerosis (MS) patients than standard gadolinium-DTPA. This enhanced detection improves assessment of disease activity and treatment efficacy in MS clinical trials.
Area of Science:
- Radiology
- Neurology
- Medical Imaging
Background:
- Contrast-enhanced magnetic resonance imaging (MRI) is crucial for evaluating disease activity in multiple sclerosis (MS).
- It serves as a potential outcome measure for assessing therapeutic efficacy in clinical trials.
- Comparing different contrast agents is essential for optimizing diagnostic sensitivity.
Purpose of the Study:
- To compare the sensitivity of a high dose of gadolinium-HP-DO3A against a standard dose of gadolinium-DTPA.
- To evaluate the impact of contrast agent dose on detecting active lesions in relapsing-remitting MS.
Main Methods:
- 16 patients with relapsing-remitting MS in the acute phase underwent two MRI scans within 48 hours.
- The first MRI used a standard dose of gadolinium-DTPA (0.1 mmol/kg).
- The second MRI used an experimental high dose of gadolinium-HP-DO3A (0.3 mmol/kg).
Main Results:
- The high-dose gadolinium-HP-DO3A study identified significantly more enhancing lesions (56) compared to the standard-dose gadolinium-DTPA (38).
- This difference was particularly notable for infratentorial and smaller lesions.
- A marked improvement in lesion visibility and delineation was observed with the higher dose contrast agent.
Conclusions:
- High-dose gadolinium-HP-DO3A demonstrates superior sensitivity in detecting active lesions in MS compared to standard gadolinium-DTPA.
- This enhanced sensitivity can improve the assessment of MS disease activity.
- Gadolinium-HP-DO3A may offer a more effective tool for MS clinical trials.
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