Literature DB >> 21566112

Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigrees.

Yiannis Athanasiou1, Konstantinos Voskarides, Daniel P Gale, Loukas Damianou, Charalambos Patsias, Michalis Zavros, Patrick H Maxwell, H Terence Cook, Panayiota Demosthenous, Andreas Hadjisavvas, Kyriacos Kyriacou, Ioanna Zouvani, Alkis Pierides, Constantinos Deltas.   

Abstract

BACKGROUND AND OBJECTIVES: Complement factor H and related proteins (CFHR) are key regulators of the alternative complement pathway, where loss of function mutations lead to a glomerulopathy with isolated mesangial C3 deposits without immunoglobulins. Gale et al. (12) reported on 26 patients with the first familial, hematuric glomerulopathy caused by a founder mutation in the CFHR5 gene in patients of Cypriot descent living in the United Kingdom. CFHR5 nephropathy is clinically characterized by continuous microscopic hematuria whereas some patients present with additional episodes of synpharyngitic macrohematuria, associated with infection and pyrexia. A subgroup of patients, particularly men, develop additional proteinuria, hypertension, and chronic renal disease or ESRD. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: We herewith expand significantly on the study by Gale et al., reporting on histologic, molecular, and clinical findings in 91 patients from 16 families with the same founder mutation.
RESULTS: Eighty-two patients (90%) exhibited microscopic hematuria; 51 (62%), exhibited only microscopic hematuria, whereas the remaining 31 additionally had proteinuria (38%); 28 proteinuric patients developed chronic renal failure (CRF). Among carriers of CFHR5 mutation aged >50 years, 80% of the men and 21% of the women developed CRF; 18 developed ESRD (14 men [78%], 4 women [22%]).
CONCLUSIONS: The diagnosis of CFHR5-related, isolated C3 glomerulopathy was established in 2009 using newly described mutation analysis after decades of follow-up with unclear diagnoses, occasionally confused with IgA nephropathy. This larger patient cohort establishes the clinical course, significant variable expressivity, and marked gender difference regarding the development of CRF and ESRD.

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Year:  2011        PMID: 21566112      PMCID: PMC3109942          DOI: 10.2215/CJN.09541010

Source DB:  PubMed          Journal:  Clin J Am Soc Nephrol        ISSN: 1555-9041            Impact factor:   8.237


  32 in total

1.  Clinicopathological features in patients with isolated C3 mesangial proliferative glomerulonephritis.

Authors:  C Manno; A R Proscia; E Laraia; M Giangrande; M Di Carlo; C Salvatore; A Tasco; F P Schena
Journal:  Nephrol Dial Transplant       Date:  1990       Impact factor: 5.992

2.  Dense deposit disease is not a membranoproliferative glomerulonephritis.

Authors:  Patrick D Walker; Franco Ferrario; Kensuke Joh; Stephen M Bonsib
Journal:  Mod Pathol       Date:  2007-03-30       Impact factor: 7.842

3.  Human factor H-related protein 5 (FHR-5). A new complement-associated protein.

Authors:  J L McRae; P J Cowan; D A Power; K I Mitchelhill; B E Kemp; B P Morgan; B F Murphy
Journal:  J Biol Chem       Date:  2000-10-31       Impact factor: 5.157

4.  Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families.

Authors:  Ilaria Longo; Elisa Scala; Francesca Mari; Rossella Caselli; Chiara Pescucci; Maria Antonietta Mencarelli; Caterina Speciale; Marisa Giani; Elena Bresin; Domenica Angela Caringella; Zvi-Uri Borochowitz; Komudi Siriwardena; Ingrid Winship; Alessandra Renieri; Ilaria Meloni
Journal:  Nephrol Dial Transplant       Date:  2005-12-07       Impact factor: 5.992

5.  Benign familial hematuria due to mutation of the type IV collagen alpha4 gene.

Authors:  H H Lemmink; W N Nillesen; T Mochizuki; C H Schröder; H G Brunner; B A van Oost; L A Monnens; H J Smeets
Journal:  J Clin Invest       Date:  1996-09-01       Impact factor: 14.808

6.  Clinicopathologic features, outcome, and therapeutic interventions in four children with isolated C3 mesangial proliferative glomerulonephritis.

Authors:  Kazuro Yagi; Hidehiko Yanagida; Keisuke Sugimoto; Hiroaki Kuwajima; Nobutada Tabata; Kosuke Morita; Mitsuru Okada; Tsukasa Takemura
Journal:  Pediatr Nephrol       Date:  2005-06-10       Impact factor: 3.714

7.  Meta-analysis of genotype-phenotype correlation in X-linked Alport syndrome: impact on clinical counselling.

Authors:  Oliver Gross; Kai-Olaf Netzer; Romy Lambrecht; Stefan Seibold; Manfred Weber
Journal:  Nephrol Dial Transplant       Date:  2002-07       Impact factor: 5.992

8.  Rat mesangial cells exhibit sex-specific profibrotic and proinflammatory phenotypes.

Authors:  Izabella Z A Pawluczyk; Eddie K C Tan; Kevin P G Harris
Journal:  Nephrol Dial Transplant       Date:  2009-01-07       Impact factor: 5.992

9.  Long-term evolution of patients with isolated C3 mesangial glomerulonephritis.

Authors:  J Calls Ginesta; J Almirall; A Torras; A Darnell; L Revert
Journal:  Clin Nephrol       Date:  1995-04       Impact factor: 0.975

Review 10.  Alport syndrome and thin glomerular basement membrane nephropathy: a practical approach to diagnosis.

Authors:  Mark Haas
Journal:  Arch Pathol Lab Med       Date:  2009-02       Impact factor: 5.534

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  61 in total

Review 1.  Exploring the genetic basis of early-onset chronic kidney disease.

Authors:  Asaf Vivante; Friedhelm Hildebrandt
Journal:  Nat Rev Nephrol       Date:  2016-01-11       Impact factor: 28.314

Review 2.  CFHR Gene Variations Provide Insights in the Pathogenesis of the Kidney Diseases Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy.

Authors:  Peter F Zipfel; Thorsten Wiech; Emma D Stea; Christine Skerka
Journal:  J Am Soc Nephrol       Date:  2020-01-24       Impact factor: 10.121

3.  Distinct roles for the complement regulators factor H and Crry in protection of the kidney from injury.

Authors:  Jennifer Laskowski; Brandon Renner; Moglie Le Quintrec; Sarah Panzer; Jonathan P Hannan; Danica Ljubanovic; Marieta M Ruseva; Dorin-Bogdan Borza; Alexandra H Antonioli; Matthew C Pickering; V Michael Holers; Joshua M Thurman
Journal:  Kidney Int       Date:  2016-05-07       Impact factor: 10.612

4.  C3 glomerulopathy: clinicopathologic features and predictors of outcome.

Authors:  Nicholas R Medjeral-Thomas; Michelle M O'Shaughnessy; John A O'Regan; Carol Traynor; Michael Flanagan; Limy Wong; Chia Wei Teoh; Atif Awan; Mary Waldron; Tom Cairns; Patrick O'Kelly; Anthony M Dorman; Matthew C Pickering; Peter J Conlon; H Terence Cook
Journal:  Clin J Am Soc Nephrol       Date:  2013-10-31       Impact factor: 8.237

5.  Efficacy of Targeted Complement Inhibition in Experimental C3 Glomerulopathy.

Authors:  Marieta M Ruseva; Tao Peng; Melissa A Lasaro; Keith Bouchard; Susan Liu-Chen; Fang Sun; Zhao-Xue Yu; Andre Marozsan; Yi Wang; Matthew C Pickering
Journal:  J Am Soc Nephrol       Date:  2015-06-05       Impact factor: 10.121

6.  C4d Staining in the Diagnosis of C3 Glomerulopathy.

Authors:  H Terence Cook
Journal:  J Am Soc Nephrol       Date:  2015-05-19       Impact factor: 10.121

Review 7.  Update on membranoproliferative GN.

Authors:  Naveed Masani; Kenar D Jhaveri; Steven Fishbane
Journal:  Clin J Am Soc Nephrol       Date:  2014-01-09       Impact factor: 8.237

Review 8.  Reclassification of membranoproliferative glomerulonephritis: Identification of a new GN: C3GN.

Authors:  Maurizio Salvadori; Giuseppina Rosso
Journal:  World J Nephrol       Date:  2016-07-06

9.  Defining the complement biomarker profile of C3 glomerulopathy.

Authors:  Yuzhou Zhang; Carla M Nester; Bertha Martin; Mikkel-Ole Skjoedt; Nicole C Meyer; Dingwu Shao; Nicolò Borsa; Yaseelan Palarasah; Richard J H Smith
Journal:  Clin J Am Soc Nephrol       Date:  2014-10-23       Impact factor: 8.237

Review 10.  Treatment options for C3 glomerulopathy.

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

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