Intestinal Phosphate Transporter Expression in CKD Patients

Chronic Kidney Diseases Clinical Trial

— PeTRA  

Official title:

Joint Study on Intestinal Phosphate-TRAnsporter Expression in CKD Patients

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02539680
• Other study ID #: 14-145
• Status: Terminated
• Phase: N/A
• First received: August 25, 2015
• Last updated: November 22, 2017
• Start date: September 2015
• Est. completion date: November 2017

Study information

• Verified date: April 2017
• Source: RWTH Aachen University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of the present study is to study the expression of the various phosphate transporters in patients with normal or moderately impaired renal function or in patients on dialysis. In particular, the investigators want to clarify whether NaPi-IIb expression level decreases in CKD patients, which would render it a potentially inadequate pharmaceutical target in these patients.

Description:

Elevated serum phosphate is a potent predictor of death and cardiovascular events in patients with renal disease. Control of serum-phosphate to desired target ranges is insufficient in many patients with advanced chronic kidney disease (CKD), in particular dialysis patients despite dietary restrictions, optimized dialysis regimens and the use of phosphate binders. One reason why for example, phosphate binders are insufficient to control phosphate uptake in the intestine or why they even loose efficacy, is a compensatory upregulation of phosphate transporters in the gut wall.

Thus, several companies attempt to specifically interfere with intestinal phosphate transporters, in particular the NaPi-IIb transporter. However, recent Chugai data obtained in experimental CKD challenge the assumption that NaPi-IIb is the major therapeutic target in this situation. In addition to NaPi-IIb, PiT-1 and -2 also might contribute to phosphate transport.

In normal human intestinal mucosa the most prominent expression of all 3 transporters is observed in the duodenum, i.e. an area, which can easily be assessed by endoscopy.

During endoscopy a biopsy for research purposes will be obtained. Chugai will evaluate the expression level of NaPi-IIb, PiT-1, PiT-2, and villin1 at the mRNA and, if possible, the protein level.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 18
• Est. completion date: November 2017
• Est. primary completion date: October 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Upper endoscopy for suspected or known esophageal or gastric pathology

• Upper endoscopy for screening purposes

• Written consent to take part in the study

Exclusion Criteria:

• Food intake within 8 hours prior to the endoscopy

• Major duodenal pathology, in particular duodenitis or duodenal ulcers or tumor

• Contraindication to duodenal biopsy such as bleeding disorder

• Treatment with medication known to regulate the expression or activity of intestinal phosphate transporters (e.g. nicotinamide)

• Kidney transplant patients

• Alcohol or drug abuse

• Mental condition rendering the subject unable to understand the nature, scope and possible consequences of the study

• Participation in a parallel clinical trial

• Subjects who are in any state of dependency to the sponsor or the investigators

• Employees of the sponsor or the investigators

• Subjects who have been committed to an institution by legal or regulatory order

Related Conditions & MeSH terms

• Chronic Kidney Diseases
• Kidney Diseases
• Renal Insufficiency, Chronic

Intervention

Procedure:
• endoscopy
duodenal biopsies

Locations

Country	Name	City	State
Germany	University Hospital Aachen	Aachen	NRW

Sponsors (2)

Lead Sponsor	Collaborator
RWTH Aachen University	Chugai Pharmaceutical

Country where clinical trial is conducted

Germany, 

References & Publications (3)

Block GA, Klassen PS, Lazarus JM, Ofsthun N, Lowrie EG, Chertow GM. Mineral metabolism, mortality, and morbidity in maintenance hemodialysis. J Am Soc Nephrol. 2004 Aug;15(8):2208-18. — View Citation

Lee GJ, Marks J. Intestinal phosphate transport: a therapeutic target in chronic kidney disease and beyond? Pediatr Nephrol. 2015 Mar;30(3):363-71. doi: 10.1007/s00467-014-2759-x. Epub 2014 Feb 5. Review. — View Citation

Marks J, Debnam ES, Unwin RJ. The role of the gastrointestinal tract in phosphate homeostasis in health and chronic kidney disease. Curr Opin Nephrol Hypertens. 2013 Jul;22(4):481-7. doi: 10.1097/MNH.0b013e3283621310. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Differences in the expression level of phosphate transporters in the duodenal of the populations		5 months