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Liver Transplantation: Skeletal Effects

Skeletal Effects of Liver Transplantation

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03399227
Enrollment
0
Registered
2018-01-16
Start date
2020-06-01
Completion date
2023-03-31
Last updated
2020-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Liver Diseases, Osteoporosis, Transplant-Related Disorder

Keywords

Bone microarchitecture

Brief summary

Fifty patients awaiting liver transplantation and 50 age and gender matched control subjects with normal liver function will be included in the study. The aim of this project is to compare liver transplantation recipients'bone microarchitecture with healthy controls and to evaluate patients' changes within one year after transplantation

Detailed description

Background: Solid organ transplantation recipients have a high prevalence of osteoporosis and fragility fractures. Deteriorated bone architecture has been shown by high resolution computed tomography (HR-pQCT) in kidney and lung transplantation recipients. In liver transplantation (LeTx) recipients, bone microarchitecture has only been evaluated using the trabecular bone score in a retrospective cohort study; a degraded or partially degraded microarchitecture was detected in most of the patients. Aim: The aim of this project is to compare LeTx recipients' bone microarchitecture with healthy controls and to evaluate patients' changes within one year after transplantation. Methods: HR-pQCT scans of the distal radius and tibia as well as areal bone mineral density measurement of the lumbar spine and hip region will be performed before Tx, 1 and 12 months after Tx in 50 patients. Anabolic and catabolic markers of bone turnover (sclerostin, dickkopf 1, periostin) and traditional bone turnover markers will be evaluated preoperatively, on the day of surgery, and 4 times within the first year after LeTx. In healthy age- and sex-matched controls HR-pQCT, bone mineral density and laboratory parameters will be assessed once. Hypotheses: Based on the HR-pQCT data of kidney and lung transplantation recipients and the trabecular bone score of LeTx recipients, the investigators hypothesize that LeTX recipients have deteriorated bone microarchitecture. Expected outcome: Since bone fragility is not only determined by BMD but bone architecture as well, HR-pQCT data give important information on the patients' bone fragility. The knowledge of the course of bone microarchitecture after liver transplantation may help to develop strategies preventing fragility fractures in LeTx recipients.

Interventions

None listed

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Women, men awaiting liver Transplantation * 20-70 years of age

Exclusion criteria

* Subjects with a history of prior solid organ transplantation * Subjects awaiting a combined liver-kidney transplantation * Cancer within the previous 5 years - except for hepatocellular carcinoma, neuroendocrine tumors and hemangioendothelioma with indication for liver transplantation * Rheumatoid arthritis * Severe renal insufficiency (chronic kidney disease IV, V) * Immobilisation * Intake of drugs with potential effects on BMD like lithium, estrogen-replacement therapy, selective Estrogen-receptor modulators, oral bisphosphonates in the last three months, denosumab and parenteral bisphosphonates in the last year - except calcium, vitamin D and medication necessary for the underlying disease * Non-osteoporotic bone disease * Recent fragility fracture within 6 months Control group: Inclusion Criteria: * Women, men * 20-70 years of age * Normal liver function (defined as liver function parameters and transaminases, such as albumin, thromboplastin time, alanine-aminotransferase, aspartate-aminotransferase, and gamma-glutamyl-transferase within the normal range) Additional

Design outcomes

Primary

MeasureTime frameDescription
Bone microarchitecture of the distal radius12 months to posttransplantationtrabecular bone mineral density measurement (XCT)

Secondary

MeasureTime frameDescription
Bone microarchitecture of the distal radiuspretransplantation to 12 after transplantationbone volume fraction (%)

Other

MeasureTime frameDescription
Bone mineral densitypretransplantation to 12 after transplantationareal bone density measurement of the lumbar spine (T score)
Biochemicalpretransplantation to 12 after transplantationSerum levels of osteocalcin

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026