Sclerostin and Vascular Calcification in CKD and Renal Transplant

NCT ID: NCT04066855

Last Updated: 2019-08-26

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 36 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2019-12-31
• Study Completion Date: 2020-09-30

Brief Summary

the aim of the research is to determine the degree of vascular calcification in chronic kidney disease and post-transplant and whether there is a correlation with the level of serum sclerostin.

Detailed Description

Sclerostin is a 22-kDa glycoprotein encoded by the SOST gene. This glycoprotein is almost exclusively synthesized by osteocytes that are not present near the bone surface but lie in the mineralized cortical and cancellous bone (3).

Sclerostin can exert its inhibitory effects on bone formation by not only inhibiting proliferation, differentiation and function of osteoblast cells but also facilitating their apoptosis(4).

Wnt/β-catenin signalling pathway participates in bone homeostasis and diseases.(5,6) But beyond that, many lines of evidence derived from cell cultures and animal studies indicate that this signalling pathway plays a prominent role in the pathogenesis of atherosclerosis and vascular calcification(VC) (7-10).

Serum sclerostin levels in CKD patients are remarkably higher than those in the normal population, with their values increasing across the CKD stages(4,11).

However; the studies on the association of serum sclerostin with VC and mortality in renal disease patients have yielded conflicting results. Some investigations showed a positive correlation, whereas others suggested no or even negative correlation(12).

VC occurs frequently in CKD patients and its incidence increases across the CKD stages (19). Notably, VC is associated with cardiovascular events (CVEs) and poor prognosis in CKD. It is well recognized that VC occurs in the early years of kidney disease patients recently, even prior to the occurrence of disordered phosphate homeostasis.VC is recognized as a pathological process of osteogenesis initiated by inflammatory factors in vessels(20).

The upregulation of sclerostin in calcified tissues led researchers and clinicians to come up with a hypothesis that sclerostin may be related to the pathogenic mechanism of VC in renal disease patients, leading to a large number of studies to examine the association between sclerostin and VC in CKD patients. However, these studies reported inconsistent results, with some studies showing positive association between sclerostin and VC in CKD patients,(21-24) whereas others showing negative association (25-28) or no association at all(29).

As in CKD patients, kidney transplant recipients' (KTRs') VC strongly predicts cardiovascular events and all-cause mortality over conventional risk factors.

Conditions

Vascular Calcification; Chronic Kidney Failure

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Study Groups

Chronic Kidney Disease (CKD)

patients diagnosed as CKD

No interventions assigned to this group

Renal transplant

recipients of renal transplantation

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Chronic Kidney disease stages 4 and 5
• Renal transplant recipients

Exclusion Criteria

• Significant co-morbidity: advanced cancer, advanced liver disease, tertiary hyperparathyroidism

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Ahmed Faisal Mohamed Mohamed Saleh

OTHER

Sponsor Role: lead

Responsible Party

Ahmed Faisal Mohamed Mohamed Saleh

Principal Investigator

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Ahmed FMM Saleh, MSc

Role: PRINCIPAL_INVESTIGATOR

Assiut University

Central Contacts

Ahmed FMM Saleh, MSc

Role: CONTACT

a-faisal-mm@hotmail.com

+201095066331

References

Li Z, Qin Y, Du L, Luo X. An improvement of carotid intima-media thickness and pulse wave velocity in renal transplant recipients. BMC Med Imaging. 2018 Aug 17;18(1):23. doi: 10.1186/s12880-018-0263-7.

Reference Type: BACKGROUND

PMID: 30119645 (View on PubMed)

Other Identifiers

Sclerostin-Vas-CKD

Identifier Type: -

Identifier Source: org_study_id