Liver transplantation for familial amyloidotic polyneuropathy: impact on Swedish patients' survival
2009 (English)In: Liver transplantation, ISSN 1527-6465, E-ISSN 1527-6473, Vol. 15, no 10, 1229-1235 p.Article in journal (Refereed) Published
Liver transplantation (LTx) for familial amyloidotic polyneuropathy (FAP) is an accepted treatment for this fatal disease. However, the long-term outcome with respect to that of nontransplanted patients has not been fully elucidated. The aim of this study was to compare the long-term survival of Swedish LTx FAP patients with that of historical controls, especially with respect to the age at onset of the disease and gender. In order to evaluate the outcome of LTx as a treatment for FAP, survival was calculated from the onset of disease. One hundred forty-one FAP patients, 108 transplanted and 33 not transplanted, were included in the study. Significantly increased survival was noted for LTx patients in comparison with controls. The outcome was especially favorable for those with an early onset of the disease (age at onset < 50 years) in comparison with early-onset controls (P < 0.001). In contrast, no significant difference for late-onset cases (> or = 50 years) was found. Transplanted late-onset females had significantly improved survival in comparison with transplanted late-onset males (P = 0.02). We were unable to find significant differences in survival between patients with long (> or = 7 years) or short (<7 years) disease duration at transplantation. The survival of male patients with late-onset disease appeared not to improve with LTx. LTx is an efficacious treatment for improving the survival of early-onset FAP patients. Further studies are needed to analyze the cause of the poorer outcome for late-onset male patients.
Place, publisher, year, edition, pages
John Wiley & Sons, 2009. Vol. 15, no 10, 1229-1235 p.
Public Health, Global Health, Social Medicine and Epidemiology
Research subject Medicine
IdentifiersURN: urn:nbn:se:umu:diva-31345DOI: 10.1002/lt.21817PubMedID: 19790145OAI: oai:DiVA.org:umu-31345DiVA: diva2:292590