Secondary osteoporosis in liver transplant recipients: a longitudinal study in patients with and without cholestatic liver disease

Scand J Gastroenterol. 2003 Mar;38(3):320-7.

Abstract

Background: Metabolic bone disease is one of the major long-term complications in liver transplant recipients, but it remains unclear which patients are at highest risk for developing severe bone disease following transplantation.

Methods: A total of 46 consecutive, adult patients with chronic liver disease accepted for a liver transplantation waiting list were prospectively included in the study. The patients were classified into two groups: group A--chronic cholestatic liver disease (n = 28), and group B--chronic non-cholestatic liver disease (n = 18). Bone mineral density (BMD) was measured at acceptance for the waiting list and at 3, 12 and 36 months following transplantation. Markers of bone turnover (serum-bone specific alkaline phosphatases (bALP), s-osteocalcin, s-1-collagen-C-terminal telopeptide (1-CTP) and urine N-terminal telopeptides u-Ntx) were measured at acceptance and at 3, 6, 12, 24 and 36 months following transplantation. BMD and markers of bone turnover were compared with similar values in a matched control group of 42 healthy individuals.

Results: BMD decreased significantly during the early post-transplantation period (median bone loss femoral neck (FN) 3 months post-transplant 8.5%). BMD levels declined slightly from 3 to 12 months following transplantation and increased thereafter. The relative bone loss was greatest among group B patients (relative bone loss FN 3 months post-transplant: group A, 8% versus group B, 13%; P = 0.04). At 36 months, 8/17 group A and 2/9 group B patients had BMD levels that exceeded the pretransplant levels (P = 0.12). The early bone loss was positively correlated with an increase in resorption markers (s-1-CTP and u-Ntx). Group B had higher levels of both s-1-CTP and u-Ntx at 3 and 6 months post-transplant than group A patients (P = 0.03). Bone formation markers increased slowly from 6 months post-transplant and onwards. Relative bone loss was positively correlated to total glucocorticoid dose during the first 3 months post-transplant. There were no differences in BMD between patients receiving tacrolimus versus those receiving cyclosporin A.

Conclusion: Bone loss following liver transplantation is considerable in patients with both cholestatic and non-cholestatic liver disease, the first group has the poorest starting-point while the latter group has the greatest bone loss following transplantation. Bone loss is closely correlated with biochemical markers of bone resorption and total dose of glucocorticoids given post-transplant.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Aged
  • Alkaline Phosphatase / blood
  • Alkaline Phosphatase / drug effects
  • Biomarkers / blood
  • Bone Density / drug effects
  • Bone Density / physiology
  • Bone Resorption / blood
  • Bone Resorption / chemically induced
  • Bone Resorption / physiopathology
  • Cholestasis / blood
  • Cholestasis / epidemiology
  • Cholestasis / therapy
  • Collagen / blood
  • Collagen / drug effects
  • Collagen Type I
  • Cyclosporine / therapeutic use
  • Female
  • Femur Neck / drug effects
  • Follow-Up Studies
  • Forearm
  • Fractures, Bone / blood
  • Fractures, Bone / etiology
  • Fractures, Bone / physiopathology
  • Glucocorticoids / therapeutic use
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Liver Diseases / blood
  • Liver Diseases / epidemiology
  • Liver Diseases / therapy
  • Liver Transplantation*
  • Longitudinal Studies
  • Lumbar Vertebrae / drug effects
  • Male
  • Middle Aged
  • Norway / epidemiology
  • Osteocalcin / blood
  • Osteocalcin / drug effects
  • Osteoporosis / blood
  • Osteoporosis / etiology*
  • Osteoporosis / physiopathology
  • Peptide Fragments / blood
  • Peptide Fragments / drug effects
  • Peptides / blood
  • Peptides / drug effects
  • Postoperative Complications / blood
  • Postoperative Complications / epidemiology
  • Postoperative Complications / etiology
  • Survival Analysis
  • Tacrolimus / therapeutic use
  • Treatment Outcome
  • Waiting Lists

Substances

  • Biomarkers
  • Collagen Type I
  • Glucocorticoids
  • Immunosuppressive Agents
  • Peptide Fragments
  • Peptides
  • collagen type I trimeric cross-linked peptide
  • glutamyl-lysyl-alanyl-histidyl-aspartyl-glycyl-glycyl-arginine
  • Osteocalcin
  • Cyclosporine
  • Collagen
  • Alkaline Phosphatase
  • Tacrolimus