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| ID | Type | Description | Link |
|---|---|---|---|
| 2024-A02004-43 | Other Identifier | IDRCB |
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In liver transplantation, the main problem is the shortage of grafts due to the small pool of donors. In order to increase the number of donors, grafts are increasingly being taken from older donors, known as 'expanded criteria' donors, who have liver steatosis lesions. Currently, expanded criteria donors account for 75% of liver transplants, whereas in 2009 they accounted for less than 30% of liver transplants.
Steatosis and its progression Non-alcoholic steatohepatitis (NASH) is an emerging disease in industrialised countries due to obesity, and corresponds to the accumulation of intracytoplasmic triglycerides.
Steatosis is diagnosed when this fat content represents more than 5% of the total liver mass. There are two types of steatosis: microvesicular steatosis and macrovacuolar steatosis, defined by the presence of lipid droplets larger than the nucleus with a nucleus displaced to the periphery. Macrovacuolar steatosis is responsible for impaired liver function if it is present in ≥30% of hepatocytes. It is a factor in poor prognosis for liver transplants, with reduced graft and recipient survival and an increase in early graft dysfunction after liver transplantation. The quantification of hepatic steatosis is based on the pathological analysis of a liver biopsy, which is currently the gold standard.
This technique has disadvantages: it is an invasive method, requiring an experienced pathologist, and presents inter-individual variability in the assessment and quantification of steatosis.
It is therefore essential to develop new non-invasive diagnostic tools that can identify the presence of steatosis > 5% and ≥ 30%. Several non-invasive techniques for diagnosing steatosis have been studied: Fibroscan, CT scan, MRI, but none of those studied previously allow for the accurate quantification of hepatic steatosis, particularly macrovacuolar steatosis, with instant results.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| liver grafts | Experimental |
| |
| Surgical specimens (hepatectomy) | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Near-infrared spectrometer | Device | Scan of the liver via near-infrared spectrometer |
|
| Measure | Description | Time Frame |
|---|---|---|
| Sensibility of near-infrared spectroscopy | Estimate the performance of near-infrared spectroscopy for quantifying hepatic steatosis (>5%). | through study completion, an average of 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| Specificity of the near-infrared spectroscopy | From enrollement to the end of the study at 12 months | |
| Youden's index of the near-infrared spectroscopy | From enrollement to the end of the study at 12 months |
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Inclusion Criteria:
Liver grafts:
Surgical specimens (hepatectomy):
Exclusion Criteria:
Liver grafts:
Surgical specimens (hepatectomy):
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Sophie Chopinet, Dr | Contact | 0491435817 | +33 | promotion.interne@ap-hm.fr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Timone Hospital | Marseille | 13005 | France |
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| ID | Term |
|---|---|
| D005234 | Fatty Liver |
| ID | Term |
|---|---|
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |
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| Likelihood index + and - of the near-infrared spectroscopy | From enrollment to the end of the study at 12 months |
| Nanogram likelihood ratio of the near-infrared spectroscopy | From enrollement to the end of the study at 12 months |
| ROC curve of the near-infrared spectroscopy | From enrollement to the end of the study at 12 months |