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Tumor necrosis factor gene polymorphism and cardiac allograft vasculopathy

Ternström, Lisa, 1972 (author)
Gothenburg University,Göteborgs universitet,Hjärt-kärlinstitutionen,Cardiovascular Institute
Jeppsson, Anders, 1960 (author)
Gothenburg University,Göteborgs universitet,Hjärt-kärlinstitutionen,Cardiovascular Institute
Ricksten, Anne, 1957 (author)
Gothenburg University,Göteborgs universitet,Institutionen för laboratoriemedicin, Avdelningen för klinisk kemi/transfusionsmedicin,Institute of Laboratory Medicine, Dept of Clinical Chemistry/Transfusion Medicine
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Nilsson, Folke, 1950 (author)
Gothenburg University,Göteborgs universitet,Hjärt-kärlinstitutionen,Cardiovascular Institute
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 (creator_code:org_t)
2005
2005
English.
In: J Heart Lung Transplant. - 1053-2498. ; 24:4, s. 433-8
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: Cardiac allograft vasculopathy (CAV) limits survival after cardiac transplantation. Tumor necrosis factor-alpha (TNF-alpha) may be a key factor in the development of CAV. Two bi-allelic polymorphisms associated with high TNF-alpha production have been identified in the TNF gene locus, TNFA1/2, at position -308 and TNFB1/2 at +252. We hypothesized that recipient TNFA2 and TNFB2 homozygosity is associated with the development of CAV after heart transplantation. METHODS: TNF gene polymorphisms were analyzed by multiplex fluorescent solid-phase mini-sequencing in 70 cardiac transplant recipients. Recipients homozygous for TNFA2 or TNFB2 (Group A, n = 29) were compared with recipients heterozygous or homozygous for TNFA1 and TNFB1 (Group B, n = 41). Coronary arteriography was performed annually or when indicated. Cumulative freedom from CAV and survival was calculated according to the Kaplan-Meier test. RESULTS: Mean follow-up was 3.8 +/- 0.3 years. In Group A, 11 of 29 recipients (38%) developed CAV compared with 9 of 41 (22%) in Group B (p = 0.12). Cumulative freedom from CAV at 3 years was 42% in Group A and 80% in Group B (p = 0.043). In Group A, 11 of 29 recipients (38%) died during follow-up compared with 4 of 41 (10%) in Group B (p = 0.006). Cumulative survival at 3 years was 72% in Group A and 93% in Group B (p = 0.003). CONCLUSIONS: The results suggest that TNFA2 and TNFB2 allele homozygosity is associated with cardiac allograft vasculopathy and mortality in heart transplant recipients.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kirurgi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Surgery (hsv//eng)

Keyword

Adult
Coronary Angiography
Coronary Arteriosclerosis/*blood/etiology/radiography
Coronary Vessels/*pathology
Female
Follow-Up Studies
Gene Frequency
Genetic Markers
Graft Rejection/blood/prevention & control
Graft Survival/genetics
Heart Transplantation/*adverse effects/mortality
Humans
Immunosuppressive Agents/therapeutic use
Male
Middle Aged
Polymerase Chain Reaction
*Polymorphism
Genetic
Prospective Studies
Survival Rate
Transplantation
Homologous
Tumor Necrosis Factor-alpha/biosynthesis/*genetics

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ref (subject category)
art (subject category)

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University of Gothenburg

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