Literature DB >> 30369521

Predictive factors for poor outcome in pediatric C3 glomerulonephritis.

Mamiko Hosoya1, Yukihiko Kawasaki1, Ryo Maeda1, Masatoki Sato1, Kazuhide Suyama1, Koichi Hashimoto1, Mitsuaki Hosoya1.   

Abstract

BACKGROUND: To clarify the predictive factors for poor outcome in pediatric C3 glomerulonephritis (C3GN), we retrospectively evaluated the relationship between the clinico-pathological findings and prognosis in cases of pediatric C3GN.
METHODS: We enrolled 18 patients diagnosed with C3GN. These patients were divided into two groups, four patients in the end-stage renal disease (ESRD) group and 14 patients in non-ESRD group, based on clinical status at the last examination. Patients in the non-ESRD group were further divided into Subgroup A, consisting of 6 treatment responders, and Subgroup B, consisting of 8 non- responders. The clinical and laboratory findings, as well as the histological findings were investigated for each group.
RESULTS: The frequency of nephrotic syndrome at onset in the ESRD group was higher than that in the non-ESRD group. Before treatment and at 2 years after treatment, urinary protein excretion levels and serum creatinine levels in the ESRD group were higher than those in the non-ESRD group. The mean serum C3 and CH50 levels at 2 years after treatment in the ESRD group were lower than those in the non-ESRD group. The degree of renal injury, level of mesangial deposits and degree of alpha SMA staining at the time of the first renal biopsy in the ESRD group were all higher than those in the non-ESRD group.
CONCLUSIONS: Our results suggest that the severity of C3GN at onset and persistent complements activity are associated with poor prognosis in C3GN.

Entities:  

Keywords:  C3 glomerulonephritis; children; clinic-pathological findings; epidemiology; predictive factors for poor outcome

Mesh:

Substances:

Year:  2018        PMID: 30369521      PMCID: PMC6305788          DOI: 10.5387/fms.2018-05

Source DB:  PubMed          Journal:  Fukushima J Med Sci        ISSN: 0016-2590


  22 in total

Review 1.  C3 glomerulopathy: a new classification.

Authors:  Fadi Fakhouri; Véronique Frémeaux-Bacchi; Laure-Hélène Noël; H Terence Cook; Matthew C Pickering
Journal:  Nat Rev Nephrol       Date:  2010-07-06       Impact factor: 28.314

2.  The changing pattern of primary glomerulonephritis in Singapore and other countries over the past 3 decades.

Authors:  K-T Woo; C-M Chan; C Y Mooi; H -L-Choong; H-K Tan; M Foo; G S L Lee; V Anantharaman; C-H Lim; C-C Tan; E J C Lee; G S C Chiang; P H Tan; T H Boon; S Fook-Chong; K-S Wong
Journal:  Clin Nephrol       Date:  2010-11       Impact factor: 0.975

3.  Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome.

Authors:  Aude Servais; Véronique Frémeaux-Bacchi; Moglie Lequintrec; Rémi Salomon; Jacques Blouin; Bertrand Knebelmann; Jean-Pierre Grünfeld; Philippe Lesavre; Laure-Hélène Noël; Fadi Fakhouri
Journal:  J Med Genet       Date:  2006-10-03       Impact factor: 6.318

4.  Primary membranoproliferative glomerulonephritis on the decline: decreased rate from the 1970s to the 2000s in Japan.

Authors:  Tetsuya Kawamura; Joichi Usui; Koji Kaseda; Kenji Takada; Itaru Ebihara; Takashi Ishizu; Tadashi Iitsuka; Kentaro Sakai; Katsumi Takemura; Masaki Kobayashi; Akio Koyama; Katsuyoshi Kanemoto; Ryo Sumazaki; Noriko Uesugi; Masayuki Noguchi; Michio Nagata; Machi Suka; Kunihiro Yamagata
Journal:  Clin Exp Nephrol       Date:  2012-09-13       Impact factor: 2.801

5.  Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies.

Authors:  Aude Servais; Laure-Hélène Noël; Lubka T Roumenina; Moglie Le Quintrec; Stephanie Ngo; Marie-Agnès Dragon-Durey; Marie-Alice Macher; Julien Zuber; Alexandre Karras; François Provot; Bruno Moulin; Jean-Pierre Grünfeld; Patrick Niaudet; Philippe Lesavre; Véronique Frémeaux-Bacchi
Journal:  Kidney Int       Date:  2012-03-28       Impact factor: 10.612

6.  Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation.

Authors:  Rubén Martínez-Barricarte; Meike Heurich; Francisco Valdes-Cañedo; Eduardo Vazquez-Martul; Eva Torreira; Tamara Montes; Agustín Tortajada; Sheila Pinto; Margarita Lopez-Trascasa; B Paul Morgan; Oscar Llorca; Claire L Harris; Santiago Rodríguez de Córdoba
Journal:  J Clin Invest       Date:  2010-09-13       Impact factor: 14.808

7.  Predicting the prognosis of renal dysfunction by renal expression of alpha-smooth muscle actin in children with MPGN type 1.

Authors:  Yukihiko Kawasaki; Junzo Suzuki; Nobuko Sakai; Mieko Tanji; Hitoshi Suzuki
Journal:  Am J Kidney Dis       Date:  2003-12       Impact factor: 8.860

Review 8.  Treatment options for C3 glomerulopathy.

Authors:  Carla M Nester; Richard J Smith
Journal:  Curr Opin Nephrol Hypertens       Date:  2013-03       Impact factor: 2.894

9.  Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement.

Authors:  Sanjeev Sethi; Fernando C Fervenza; Yuzhou Zhang; Ladan Zand; Nicole C Meyer; Nicolò Borsa; Samih H Nasr; Richard J H Smith
Journal:  Kidney Int       Date:  2012-12-12       Impact factor: 10.612

Review 10.  Recent insights into C3 glomerulopathy.

Authors:  Thomas D Barbour; Matthew C Pickering; H Terence Cook
Journal:  Nephrol Dial Transplant       Date:  2013-03-10       Impact factor: 5.992

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