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The corticomedullary gradient is largely responsible for developing the gradients that are needed to concentrate urine (more solutes and less water). The ability of the kidneys to produce concentrated urine is a major determinant of the ability to survive the warm weather. When temperatures are high, we lose water through sweat, and so the kidneys retain water to maintain fluidity in the blood. The maintenance of a sodium (salt) gradient is required for urine concentration because increased medullary sodium concentration increases the reabsorption of water into the kidney, to be redistributed in the blood. The purpose of this study is to know if the corticomedullary gradient is altered in patients across a wide spectrum of kidney disease using sodium Magnetic Resonance Imaging (MRI), a machine that takes pictures and measures the salt content in the kidneys. 23Na kidney MRI, will provide functional MR of the kidney as a non-invasive tool to describe medullary function to improve management of chronic and kidney disease.
This study is a pilot exploratory study (preliminary project to assess the use of a kidney sodium coil across a wide spectrum of kidney disease). Approximately 200 patients from the London Health Sciences Regional Renal Program will be recruited. This study involves two visits at Robarts Research Institute or St. Joseph's Hospital, London, Ontario depending on scanner availability, lasting approximately 2 hours.
At the first study visit participants will undergo a sodium MRI scan of your kidneys. Prior to the scan, participants will have their sitting blood pressure and heart rate measured three times consecutively using a standard automatic blood pressure monitor. In addition to this, participants will be asked to provide a spot urine sample and have blood work done. If participants have been treated for nephrolithiasis, they will be responsible for completing a 24-hour urine volume test sometime the week before the MRI scan.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Adult CKD stage 1-5 participants |
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| Adult transplanted participants | • Age greater than or equal to 18 years |
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| Adult dialysis participants |
|
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| Adult ADPKD | • Age greater than or equal to 18 years |
| |
| Adults treated for nephrolithiasis | • Age greater than or equal to 18 years |
| |
| Adult healthy controls including kidney donors |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Sodium-23 MRI | Diagnostic Test | Participants will lay in the MRI bed for approximately 60 minutes during scanning while the MRI technologist takes detailed pictures of their kidneys. |
| Measure | Description | Time Frame |
|---|---|---|
| Exploratory cortico-medullary gradient measurement | Exploratory cortico-medullary gradient measurement in a large range of kidney disease by measuring sodium medullary to cortex ratio with23Na kidney MRI in: 1) stage 1-5 CKD patients 2) transplanted patients 3) dialysis patients 4) ADPKD patients 5) nephrolithiasis patients (characteristically associated with salt loading) 6) healthy controls including kidney donors | Throughout study visit, on average 2 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Urinary osmolarity | To evaluate the relationship between sodium medullary to cortex ratio and urinary osmolarity | Throughout study visit, on average 2 hours |
| Renal Function | To evaluate the relationship between sodium medullary to cortex ratio and renal function |
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Inclusion Criteria:
Exclusion Criteria:
Pregnant, breastfeeding or intending pregnancy
Contraindication to MRI
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CKD stage 1-5 Transplanted patients Maintenance dialysis (hemo and PD) ADPKD patient Patients treated for nephrolithiasis Healthy controls, including kidney donors
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Christopher W McIntyre, MD | Contact | 5196858500 | 58502 | christopher.mcintyre@lhsc.on.ca |
| Sandrine Lemoine, MD | Contact |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Victoria Hospital, London Health Sciences Centre | Recruiting | London | Ontario | N6A 5W9 | Canada |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 38688870 | Derived | Lemoine S, Akbari A, Brahm G, Dorie J, Tamasi T, Penny J, McIntyre CW. Redefining the concept of residual renal function with kidney sodium MRI: a pilot study. Nephrol Dial Transplant. 2024 Oct 30;39(11):1809-1816. doi: 10.1093/ndt/gfae070. |
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| ID | Term |
|---|---|
| D051436 | Renal Insufficiency, Chronic |
| D053040 | Nephrolithiasis |
| D016891 | Polycystic Kidney, Autosomal Dominant |
| ID | Term |
|---|---|
| D051437 | Renal Insufficiency |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
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Complete blood count, urea, electrolytes, calcium, phosphate, 25-hydroxyVitamin D, CRP, glucose, intact PTH, creatinine, cystatin C, and osmolality.
| Throughout study visit, on average 2 hours |
| Native and transplanted kidney | To compare sodium medullary to cortex ratio between native kidney and transplanted kidney | Throughout study visit, on average 2 hours |
| Kidney biopsy | To compare sodium medullary to cortex ratio between transplanted kidney and kidney biopsy | Throughout study visit, on average 2 hours |
| Residual renal function | To evaluate sodium medullary to cortex ratio in dialysis patients and renal residual function | Throughout study visit, on average 2 hours |
| Nephrolithiasis | To compare sodium medullary to cortex ratio between healthy control and patients who have nephrolithiasis | Throughout study visit, on average 2 hours |
| ADPKD | To evaluate the ability to measure sodium medullary to cortex ratio in autosomal dominant polycystic kidney disease | Throughout study visit, on average 2 hours |
| Clinical practice | To determinate if measurement of sodium medullary to cortex ratio measurement is meaningful in clinical practice | Throughout study visit, on average 2 hours |
| 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 |
| D052878 | Urolithiasis |
| D007690 | Polycystic Kidney Diseases |
| D052177 | Kidney Diseases, Cystic |
| D000015 | Abnormalities, Multiple |
| D000013 | Congenital Abnormalities |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D000072661 | Ciliopathies |
| D030342 | Genetic Diseases, Inborn |