Rekurrenz der IgA-nephropathie nach nierentransplantation

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Christos Bantis
  • P. J. Heering
  • Cornelia Blume
  • Sendogan Aker
  • Magdalena Siekierka
  • B. Grabensee
  • Katrin Ivens

Externe Organisationen

  • Universitätsklinikum Düsseldorf
Forschungs-netzwerk anzeigen

Details

Titel in ÜbersetzungRecurrence of IgA nephropathy after renal transplantation
OriginalspracheDeutsch
Seiten (von - bis)81-86
Seitenumfang6
FachzeitschriftNieren- und Hochdruckkrankheiten
Jahrgang36
Ausgabenummer3
PublikationsstatusVeröffentlicht - März 2007
Extern publiziertJa

Abstract

Aim of the study: In the present study, we evaluated risk factors for the development and the clinical course of recurrent IgA nephropathy (IgAN) after renal transplantation. Patients and methods: We analyzed n = 125 patients who were transplanted from 1986 to 2004 and had biopsy-proven IgAN as primary disease and n = 250 renal allograft recipients with other primary diseases. The mean follow-up period was 6.0 ± 3.6 years. Results: During follow-up, IgAN recurrence was diagnosed by transplant biopsy in n = 24 patients (19% of the cohort, 44% of the patients who underwent a transplant biopsy for any reason after the first 6 months post transplantation). The mean time from renal transplantation to the development of microscopic hematuria and histologic confirmation of IgAN recurrence was 2.8 ± 1.8 and 4.7 ± 2.6 years, respectively. Patients with biopsy-confirmed IgAN recurrence were younger compared to patients with biopsy-excluded or with no clinical signs of recurrence (37.6 ± 11 vs 44.4 ± 12 years, p < 0.05). In the Cox regression analysis, a 34% higher recurrence risk was demonstrated for every decade of age (HR 0.66, 95% CI: 0.45 - 0.96, p < 0.05). IgAN recurrence was not associated with the type of the graft (cadaveric or living donor), HLA constellation, number of acute rejection episodes or immunosuppressive and antihypertensive medications (NS). Graft survival was not influenced by the presence of IgAN recurrence (NS). There was no significant difference in graft survival between patients with IgAN and other primary diseases (NS). Conclusion: IgAN recurrence is a common complication, especially in younger renal transplant recipients, but has no impact on graft survival.

Schlagwörter

    IgA nephropathy, Kidney transplantation, Kidney transplantation: complications, Recurrence of primary disease, Renal graft survival

ASJC Scopus Sachgebiete

Zitieren

Rekurrenz der IgA-nephropathie nach nierentransplantation. / Bantis, Christos; Heering, P. J.; Blume, Cornelia et al.
in: Nieren- und Hochdruckkrankheiten, Jahrgang 36, Nr. 3, 03.2007, S. 81-86.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Bantis, C, Heering, PJ, Blume, C, Aker, S, Siekierka, M, Grabensee, B & Ivens, K 2007, 'Rekurrenz der IgA-nephropathie nach nierentransplantation', Nieren- und Hochdruckkrankheiten, Jg. 36, Nr. 3, S. 81-86. https://doi.org/10.5414/nhp36081
Bantis, C., Heering, P. J., Blume, C., Aker, S., Siekierka, M., Grabensee, B., & Ivens, K. (2007). Rekurrenz der IgA-nephropathie nach nierentransplantation. Nieren- und Hochdruckkrankheiten, 36(3), 81-86. https://doi.org/10.5414/nhp36081
Bantis C, Heering PJ, Blume C, Aker S, Siekierka M, Grabensee B et al. Rekurrenz der IgA-nephropathie nach nierentransplantation. Nieren- und Hochdruckkrankheiten. 2007 Mär;36(3):81-86. doi: 10.5414/nhp36081
Bantis, Christos ; Heering, P. J. ; Blume, Cornelia et al. / Rekurrenz der IgA-nephropathie nach nierentransplantation. in: Nieren- und Hochdruckkrankheiten. 2007 ; Jahrgang 36, Nr. 3. S. 81-86.
Download
@article{ef8a43611da5475f92533638e63e0092,
title = "Rekurrenz der IgA-nephropathie nach nierentransplantation",
abstract = "Aim of the study: In the present study, we evaluated risk factors for the development and the clinical course of recurrent IgA nephropathy (IgAN) after renal transplantation. Patients and methods: We analyzed n = 125 patients who were transplanted from 1986 to 2004 and had biopsy-proven IgAN as primary disease and n = 250 renal allograft recipients with other primary diseases. The mean follow-up period was 6.0 ± 3.6 years. Results: During follow-up, IgAN recurrence was diagnosed by transplant biopsy in n = 24 patients (19% of the cohort, 44% of the patients who underwent a transplant biopsy for any reason after the first 6 months post transplantation). The mean time from renal transplantation to the development of microscopic hematuria and histologic confirmation of IgAN recurrence was 2.8 ± 1.8 and 4.7 ± 2.6 years, respectively. Patients with biopsy-confirmed IgAN recurrence were younger compared to patients with biopsy-excluded or with no clinical signs of recurrence (37.6 ± 11 vs 44.4 ± 12 years, p < 0.05). In the Cox regression analysis, a 34% higher recurrence risk was demonstrated for every decade of age (HR 0.66, 95% CI: 0.45 - 0.96, p < 0.05). IgAN recurrence was not associated with the type of the graft (cadaveric or living donor), HLA constellation, number of acute rejection episodes or immunosuppressive and antihypertensive medications (NS). Graft survival was not influenced by the presence of IgAN recurrence (NS). There was no significant difference in graft survival between patients with IgAN and other primary diseases (NS). Conclusion: IgAN recurrence is a common complication, especially in younger renal transplant recipients, but has no impact on graft survival.",
keywords = "IgA nephropathy, Kidney transplantation, Kidney transplantation: complications, Recurrence of primary disease, Renal graft survival",
author = "Christos Bantis and Heering, {P. J.} and Cornelia Blume and Sendogan Aker and Magdalena Siekierka and B. Grabensee and Katrin Ivens",
year = "2007",
month = mar,
doi = "10.5414/nhp36081",
language = "Deutsch",
volume = "36",
pages = "81--86",
number = "3",

}

Download

TY - JOUR

T1 - Rekurrenz der IgA-nephropathie nach nierentransplantation

AU - Bantis, Christos

AU - Heering, P. J.

AU - Blume, Cornelia

AU - Aker, Sendogan

AU - Siekierka, Magdalena

AU - Grabensee, B.

AU - Ivens, Katrin

PY - 2007/3

Y1 - 2007/3

N2 - Aim of the study: In the present study, we evaluated risk factors for the development and the clinical course of recurrent IgA nephropathy (IgAN) after renal transplantation. Patients and methods: We analyzed n = 125 patients who were transplanted from 1986 to 2004 and had biopsy-proven IgAN as primary disease and n = 250 renal allograft recipients with other primary diseases. The mean follow-up period was 6.0 ± 3.6 years. Results: During follow-up, IgAN recurrence was diagnosed by transplant biopsy in n = 24 patients (19% of the cohort, 44% of the patients who underwent a transplant biopsy for any reason after the first 6 months post transplantation). The mean time from renal transplantation to the development of microscopic hematuria and histologic confirmation of IgAN recurrence was 2.8 ± 1.8 and 4.7 ± 2.6 years, respectively. Patients with biopsy-confirmed IgAN recurrence were younger compared to patients with biopsy-excluded or with no clinical signs of recurrence (37.6 ± 11 vs 44.4 ± 12 years, p < 0.05). In the Cox regression analysis, a 34% higher recurrence risk was demonstrated for every decade of age (HR 0.66, 95% CI: 0.45 - 0.96, p < 0.05). IgAN recurrence was not associated with the type of the graft (cadaveric or living donor), HLA constellation, number of acute rejection episodes or immunosuppressive and antihypertensive medications (NS). Graft survival was not influenced by the presence of IgAN recurrence (NS). There was no significant difference in graft survival between patients with IgAN and other primary diseases (NS). Conclusion: IgAN recurrence is a common complication, especially in younger renal transplant recipients, but has no impact on graft survival.

AB - Aim of the study: In the present study, we evaluated risk factors for the development and the clinical course of recurrent IgA nephropathy (IgAN) after renal transplantation. Patients and methods: We analyzed n = 125 patients who were transplanted from 1986 to 2004 and had biopsy-proven IgAN as primary disease and n = 250 renal allograft recipients with other primary diseases. The mean follow-up period was 6.0 ± 3.6 years. Results: During follow-up, IgAN recurrence was diagnosed by transplant biopsy in n = 24 patients (19% of the cohort, 44% of the patients who underwent a transplant biopsy for any reason after the first 6 months post transplantation). The mean time from renal transplantation to the development of microscopic hematuria and histologic confirmation of IgAN recurrence was 2.8 ± 1.8 and 4.7 ± 2.6 years, respectively. Patients with biopsy-confirmed IgAN recurrence were younger compared to patients with biopsy-excluded or with no clinical signs of recurrence (37.6 ± 11 vs 44.4 ± 12 years, p < 0.05). In the Cox regression analysis, a 34% higher recurrence risk was demonstrated for every decade of age (HR 0.66, 95% CI: 0.45 - 0.96, p < 0.05). IgAN recurrence was not associated with the type of the graft (cadaveric or living donor), HLA constellation, number of acute rejection episodes or immunosuppressive and antihypertensive medications (NS). Graft survival was not influenced by the presence of IgAN recurrence (NS). There was no significant difference in graft survival between patients with IgAN and other primary diseases (NS). Conclusion: IgAN recurrence is a common complication, especially in younger renal transplant recipients, but has no impact on graft survival.

KW - IgA nephropathy

KW - Kidney transplantation

KW - Kidney transplantation: complications

KW - Recurrence of primary disease

KW - Renal graft survival

UR - http://www.scopus.com/inward/record.url?scp=34247185251&partnerID=8YFLogxK

U2 - 10.5414/nhp36081

DO - 10.5414/nhp36081

M3 - Artikel

AN - SCOPUS:34247185251

VL - 36

SP - 81

EP - 86

JO - Nieren- und Hochdruckkrankheiten

JF - Nieren- und Hochdruckkrankheiten

SN - 0300-5224

IS - 3

ER -

Von denselben Autoren