Journal article
Treatment options for C3 glomerulopathy
Current opinion in nephrology and hypertension, Vol.22(2), pp.231-237
03/2013
DOI: 10.1097/mnh.0b013e32835da24c
PMCID: PMC4437761
PMID: 23318699
Abstract
The purpose of this review is to discuss emerging nomenclature, review the salient clinicopathological features and describe the therapeutic options available for the treatment of C3 glomerulopathy (C3G).
C3G is minimally responsive to traditional immune suppression and randomized controlled trials to support therapy are absent. The burgeoning understanding of the role of the alternative complement pathway in C3G combined with animal data supporting the use of terminal complement blockade and a few reports suggesting that the anticomplement drug eculizumab may offer a therapeutic advantage have triggered great interest in the field of complement-mediated renal disease.
Anticellular immune suppression and plasma therapy have limited efficacy in C3G. Data suggest that eculizumab may ameliorate disease in some C3G patients. The limited, recently published cohort data highlight crucial aspects of this group of diseases and support the need for extensive genetic and biomarker research to validate the pathologic mechanisms, delineate the spectrum of disease and guide the design of the rigorous trials to identify effective therapies for the treatment of C3G.
Details
- Title: Subtitle
- Treatment options for C3 glomerulopathy
- Creators
- Carla M Nester - Departments of Internal Medicine and Pediatrics, University of Iowa, Iowa City, Iowa, USA. carla-nester@uiowa.eduRichard J Smith
- Resource Type
- Journal article
- Publication Details
- Current opinion in nephrology and hypertension, Vol.22(2), pp.231-237
- DOI
- 10.1097/mnh.0b013e32835da24c
- PMID
- 23318699
- PMCID
- PMC4437761
- NLM abbreviation
- Curr Opin Nephrol Hypertens
- ISSN
- 1062-4821
- eISSN
- 1473-6543
- Publisher
- Ovid Technologies (Wolters Kluwer Health); England
- Grant note
- R01 DK074409 / NIDDK NIH HHS DK074409 / NIDDK NIH HHS
- Language
- English
- Date published
- 03/2013
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Anatomy and Cell Biology; Nephrology, Dialysis and Transplantation; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Otolaryngology; Internal Medicine
- Record Identifier
- 9984007196902771
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