Literature DB >> 23464675

Kidney diseases caused by glomerular basement membrane type IV collagen defects in dogs.

George E Lees1.   

Abstract

OBJECTIVE: To review the pathogenesis, as well as the clinical and pathologic features of canine glomerular diseases caused by genetic type IV collagen defects. DATA SOURCES: Original studies and review articles from human and veterinary medical fields. HUMAN DATA SYNTHESIS: Presence in glomerular basement membranes (GBM) of a network composed of α3.α4.α5 heterotrimers of type IV collagen is required to maintain structure and function of glomerular capillary walls. VETERINARY DATA SYNTHESIS: Hereditary nephropathy (HN) is the most commonly used name for kidney diseases that occur in dogs due to genetic type IV collagen abnormalities. To date, 4 different collagen IV gene mutations have been identified in dogs with HN; 2 are COL4A5 mutations that cause X-linked HN (XL-HN), and 2 are COL4A4 mutations that cause autosomal recessive HN (AR-HN). Affected males with XL-HN and affected males and females with AR-HN develop juvenile-onset kidney disease manifested by proteinuria typically starting at 3-6 months of age and followed by progressive kidney disease leading to terminal failure usually at 6-24 months of age. Carrier female dogs with XL-HN also develop proteinuria starting at 3-6 months of age, but progressive disease causing kidney failure is uncommon until they are >5 years old. The distinctive pathologic lesions of HN are extensive multilaminar splitting and thickening of the GBM, as demonstrated by electron microscopy, and abnormal type IV collagen α-chain content of basement membranes, as demonstrated by immunolabeling. Identification of the underlying gene mutations has permitted genetic testing and selective breeding practices that currently are minimizing HN in breeds known to be at risk.
CONCLUSIONS: Canine HN is a rare disease that should be considered whenever a dog exhibits a juvenile-onset kidney disease characterized partly by proteinuria, but highly specialized methods are required to pursue a definitive diagnosis. © Veterinary Emergency and Critical Care Society 2013.

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Year:  2013        PMID: 23464675     DOI: 10.1111/vec.12031

Source DB:  PubMed          Journal:  J Vet Emerg Crit Care (San Antonio)        ISSN: 1476-4431


  4 in total

1.  Pathological features of proteinuric nephropathy resembling Alport syndrome in a young Pyrenean Mountain dog.

Authors:  Go Sugahara; Ichiro Naito; Yuichi Miyagawa; Takaaki Komiyama; Naoyuki Takemura; Ryosuke Kobayashi; Takayuki Mineshige; Junichi Kamiie; Kinji Shirota
Journal:  J Vet Med Sci       Date:  2015-04-17       Impact factor: 1.267

2.  A novel COL4A5 mutation identified in a Chinese Han family using exome sequencing.

Authors:  Xiaofei Xiu; Jinzhong Yuan; Xiong Deng; Jingjing Xiao; Hongbo Xu; Zhaoyang Zeng; Liping Guan; Fengping Xu; Sheng Deng
Journal:  Biomed Res Int       Date:  2014-07-06       Impact factor: 3.411

3.  RNA-seq of serial kidney biopsies obtained during progression of chronic kidney disease from dogs with X-linked hereditary nephropathy.

Authors:  Candice P Chu; Jessica A Hokamp; Rachel E Cianciolo; Alan R Dabney; Candice Brinkmeyer-Langford; George E Lees; Mary B Nabity
Journal:  Sci Rep       Date:  2017-12-01       Impact factor: 4.379

4.  Allele frequency of nonsense mutation responsible for hereditary nephropathy in English cocker spaniel dogs.

Authors:  Larissa Rocha Andrade; Amanda Manara Caceres; Anelize de Souza Trecenti; Alexandre Secorun Borges; Jose Paes Oliveira-Filho
Journal:  Vet Anim Sci       Date:  2020-04-19
  4 in total

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