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Serum Preptin Level and Its Relationship with Bone Mineral Disease in Chronic Kidney Disease Patients

A

Assiut University

Status

Not yet enrolling

Conditions

Preptin

Treatments

Diagnostic Test: serum preptin

Study type

Observational

Funder types

Other

Identifiers

NCT06594042
preptin chronic kidney disease

Details and patient eligibility

About

Aim of the research:To identify preptin level and relationship with bone disease in chronic kidney disease patients.

Full description

Preptin is a 34-aminoacid peptide derived from the E-peptide of pro-insulin-like growth factor 2 (pro-IGF2) that is co-secreted with insulin and upregulates glucose-mediated insulin secretion. High serum preptin levels were described in conditions associated with insulin resistance, such as polycystic ovary syndrome and type 2 diabetes mellitus (T2M). Insulin and also IGF2 are known to be anabolic bone hormones .

Preptin stimulates osteoblastic proliferation and increases mineralization in a concentration-independent manner in osteoblast precursor cell , Despite being associated with insulin resistance, an increased fat mass has beneficial bone effects . While the increased mechanical loading favors bone formation, adipokines and also pancreatic and gut hormones were also proposed to mediate the relationship between fat and bone. The importance of nutritional hormones in maintaining bone mass was, thus, recognized. Insulin has anabolic bone effects, and hyperinsulinemia contributes to increased bone mineral density (BMD). Similar to insulin, insulin-like growth factor 1 (IGF1) and IGF2, preptin was recently proposed to have anabolic bone activity .

End-stage renal disease (ESRD) patients present with specific bone and mineral metabolism disturbances. Chronic kidney disease-associated mineral and bone disorder accounts for increased morbidity and mortality in those patients. Biochemical markers known thus far do not effectively predict the complex bone changes that are observed in ESRD patients .

Enrollment

96 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • both sex groups of patients with age between 18-50 years . pre end stage renal disease and end stage renal disease patients .

Exclusion criteria

  • type 2 diabetic patients

Trial contacts and locations

0

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Central trial contact

Seham Mohammed Ali, specialist; Mohammad Hassan Mostafa, assistant professor of interna

Data sourced from clinicaltrials.gov

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