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Sarcopenia in chronic kidney disease (CKD) affects 50% of dialysis patients and 20% of patients with non-dialyzed CKD and reduce quality of life and survival. The pathophysiology of uremic sarcopenia is multifactorial (accumulation of toxins, metabolic disturbances, etc.) and poorly characterized. These pejorative factors are associated with malnutrition and a sedentary lifestyle. Currently, there are no strategies to combat sarcopenia with the exception of physical activity, which is only possible for a limited number of patients due to their comorbidities. Developing new pharmacological strategies to combat sarcopenia is necessary.
FGF19 is a growth factor produced in the ileum involved in metabolic homeostasis. In the laboratory, a new function of FGF19 has been discovered. FGF19 acts as a hormonal factor stimulating muscle mass and strength. Preliminary studies had shown a decrease in the concentration and secretion of FGF19 in response to a meal in haemodialysis patients. However, the link between FGF19, muscle mass and CKD has never been demonstrated. The aim of this study is to assess the relationship between the concentration and secretion of FGF19 and muscle function in a large population of patients with CKD of different stages. Given the hormonal communication between the bone and the muscle, the investigators will also recover the bone histological parameters from a bone biopsy if dialysis patients are to benefit from this as part of their follow-up.
The investigators hypothesize that a decrease in FGF19 concentration and secretion in CKD is associated with a decrease in muscle mass and strength.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| CKD patients | Experimental | Patients with CKD, non-diabetic, without a history of renal transplantation, without digestive pathology, aged 18 to 70 and an estimate of the glomerular filtration rate (eGFR) <60 ml / min / 1.73m2 according to the formula of CKD-EPI. |
|
| Haemodialysis patients | Active Comparator | Patients on hemodialysis, for more than 3 months, with no history of kidney transplantation, without digestive pathology, aged 18 to 70 with a BMI between 18 and 30 kg / m2 |
|
| Healthy volunteers | Active Comparator | Healthy volunteers (controls) recruited from the population of living kidney donors or among patients from the nephrology department whose check-up shows no renal pathology |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Meal test and muscle biopsies | Procedure | The FGF19 parameters will be assessed in fasting and in postprandial period after the consumption of a hyper-carbohydrate and hyper-lipidic test meal called Flexmeal. A muscle biopsies by a needle will be performed before and after the Flexmeal. |
| Measure | Description | Time Frame |
|---|---|---|
| Correlation between the fasting plasma concentration of FGF19 and the muscle mass | Study the correlation between the fasting plasma concentration of FGF19 and the muscle mass in % of body weight, measured by DEXA scanner (Dual-X-Ray-Absorptiometry) in non-dialyzed MRC patients with a measured glomerular filtration rate (mDFG) <60 ml / min /1.73m², hemodialysis patients and healthy voluntary being assessed for a kidney donation or a nephrological check-up with no renal pathology.. | At the end of the study (55 months) |
| Measure | Description | Time Frame |
|---|---|---|
| Correlation between fasting plasma FGF19 concentration and Glomerular Filtration Rate (GFR) | Correlation between fasting plasma FGF19 concentration and Glomerular Filtration Rate (GFR) measured by a reference method (Iohexol clearance or Tc DTPA) for non-dialysis patients (in ml/min/1.73m2) | At the end of the study (55 months) |
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Inclusion Criteria:
-For the patient population:
For control group:
For all of the study participants:
o Non diabetic (fasting blood glucose <1.26 g / L, or absence of insulin or oral antidiabetic treatment)
Exclusion Criteria:
For the patient population:
For control group:
For all of the study participants:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Laetitia KOPPE, MD | Contact | +33 4 72 67 87 15 | laetitia.koppe@chu-lyon.fr | |
| Cécile BARNEL | Contact | +33 4 78 86 37 12 | cecile.barnel@chu-lyon.fr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centre Hospitalier Lyon SUD | Recruiting | Pierre-Bénite | 69310 | France |
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| ID | Term |
|---|---|
| D051436 | Renal Insufficiency, Chronic |
| ID | Term |
|---|---|
| D051437 | Renal Insufficiency |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
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|
| Correlation between fasting plasma FGF19 concentration and muscle strength |
Correlation between fasting plasma FGF19 concentration and muscle strength in kilograms in the Hand Grip |
| At the end of the study (55 months) |
| Correlation between fasting plasma FGF19 concentration and muscle performance | Correlation between fasting plasma FGF19 concentration and muscle performance assessed by the 6-minute walk test (TM6) evaluated in metres and by the SPPB (Short Physical Performance Battery) test with a score between 0 and 12 | At the end of the study (55 months) |
| Correlation between fasting plasma FGF19 concentration and muscle quality | Correlation between fasting plasma FGF19 concentration and muscle quality assessed by ultrasound (echogenicity intensity (EI) from 0 for black to 255 white and qualitatively by the Heckmatt visual assessment scale (Grade I to IV)). | At the end of the study (55 months) |
| Correlation between fasting plasma FGF19 concentration and muscle mass | Correlation between fasting plasma FGF19 concentration and muscle mass obtained by ultrasound by measuring the cross-sectional area (in mm2) of the rectus femoris muscle (RF-CSA, Rectus femoris anatomical cross-sectional area) | At the end of the study (55 months) |
| Correlation between fasting plasma FGF19 concentration and bone density | Correlation between fasting plasma FGF19 concentration and bone density determined by DEXA scan (total T-score) | At the end of the study (55 months) |
| Correlation between fasting plasma FGF19 concentration and bone quality in dialysis patients | Correlation between fasting plasma FGF19 concentration and bone quality in dialysis patients as assessed by the level of bone remodelling determined on bone biopsy (BFR/BS) | At the end of the study (55 months) |
| Correlation between fasting plasma FGF19 concentration and physical activity | Correlation between fasting plasma FGF19 concentration and physical activity assessed by the STAQ questionnaire (in hours/week) only if the primary endpoint is significant. | At the end of the study (55 months) |
| Correlation between fasting plasma FGF19 concentration and faecal bacterial microbiological profile | Correlation between fasting plasma FGF19 concentration and faecal bacterial microbiological profile by 16s sequencing of stool samples (analysis performed in a second step) | At the end of the study (55 months) |
| Correlation between fasting plasma FGF19 concentration and the number of adverse events | Correlation between fasting plasma FGF19 concentration and the number of adverse events such as mortality, cardiovascular events and fractures throughout the protocol | At the end of the study (55 months) |
| D005261 |
| Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |