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      Protocol and rationale for the first South Asian 5-year prospective longitudinal observational cohort study and biomarker evaluation investigating the clinical course and risk profile of IgA nephropathy: GRACE IgANI cohort

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          Abstract

          Background: IgA nephropathy (IgAN) is the most common primary glomerulonephritis and an important cause of end-stage kidney disease. Unlike the slowly progressive course seen among Caucasian and East Asian subjects (actuarial survival 80-85% over 10 years), in India about 30-40% of patients have nephrotic syndrome and renal dysfunction at presentation and a 10-year renal survival of 35%, as reported from a retrospective registry. These observations cannot be entirely attributed to a lack of uniform screening protocols or late referral and attest to the probability that IgAN may not be the same disease in different parts of the world.

          Methods: We will prospectively recruit 200 patients with IgAN (the GRACE IgANI— Glomerular Research And Clinical Experiments- Ig A Nephropathy in Indians—cohort) and stratify them into low and high risk of progression based on published absolute renal risk scores. We will test the validity of this risk score in an unselected Indian IgAN population over a 5-year follow-up period. In parallel, we will undertake extensive exploratory serum, urine, renal and microbiome biomarker studies, firstly, to determine if the underlying pathogenic pathways are the same in Indian IgAN compared to those reported in Caucasian and East Asian IgAN. Secondly, we will systematically assess the value of measuring selected biomarkers and adding this data to traditional measures of risk in IgAN to predict kidney failure. We ultimately hope to generate a composite IgAN risk score specific for the Indian population.

          Ethics and data dissemination: Approval was obtained from the Institutional Review Board (Silver, Research and Ethics Committee) of the Christian Medical College, Vellore, India (Ref. No. IRB Min. No. 8962 [Other] dated 23.07.2014 and IRB Min. No. 9481 [Other] dated 24.06.2015). It is anticipated that results of this study will be presented at national and international meetings, with reports being published from late 2018.

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          Most cited references39

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          Remission of proteinuria improves prognosis in IgA nephropathy.

          Proteinuria has been shown to be an adverse prognostic factor in IgA nephropathy. The benefit of achieving a partial remission of proteinuria, however, has not been well described. We studied 542 patients with biopsy-proven primary IgA nephropathy in the Toronto Glomerulonephritis Registry and found that glomerular filtration rate (GFR) declined at -0.38 +/- 0.61 ml/min per 1.73 m2/mo overall, with 30% of subjects reaching end-stage renal disease. Multivariate analysis revealed that proteinuria during follow-up was the most important predictor of the rate of GFR decline. Among the 171 patients with 3 g/d (n = 121) lost renal function 25-fold faster than those with or =3 g/d who achieved a partial remission (<1 g/d) had a similar course to patients who had < or =1 g/d throughout, and fared far better than patients who never achieved remission. These results underscore the relationship between proteinuria and prognosis in IgA nephropathy and establish the importance of remission.
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            Predicting the risk for dialysis or death in IgA nephropathy.

            For the individual patient with primary IgA nephropathy (IgAN), it remains a challenge to predict long-term outcomes for patients receiving standard treatment. We studied a prospective cohort of 332 patients with biopsy-proven IgAN patients followed over an average of 13 years. We calculated an absolute renal risk (ARR) of dialysis or death by counting the number of risk factors present at diagnosis: hypertension, proteinuria ≥1 g/d, and severe pathologic lesions (global optical score, ≥8). Overall, the ARR score allowed significant risk stratification (P < 0.0001). The cumulative incidence of death or dialysis at 10 and 20 years was 2 and 4%, respectively, for ARR=0; 2 and 9% for ARR=1; 7 and 18% for ARR=2; and 29 and 64% for ARR=3, in adequately treated patients. When achieved, control of hypertension and reduction of proteinuria reduced the risk for death or dialysis. In conclusion, the absolute renal risk score, determined at diagnosis, associates with risk for dialysis or death. Copyright © 2011 by the American Society of Nephrology
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              Glomerular activation of the lectin pathway of complement in IgA nephropathy is associated with more severe renal disease.

              IgA nephropathy (IgAN) is characterized by glomerular co-deposition of IgA and complement components. Earlier studies showed that IgA activates the alternative pathway of complement, whereas more recent data also indicate activation of the lectin pathway. The lectin pathway can be activated by binding of mannose-binding lectin (MBL) and ficolins to carbohydrate ligands, followed by activation of MBL-associated serine proteases and C4. This study examined the potential role of the lectin pathway in IgAN. Renal biopsies of patients with IgAN (n=60) showed mesangial deposition of IgA1 but not IgA2. Glomerular deposition of MBL was observed in 15 (25%) of 60 cases with IgAN and showed a mesangial pattern. All MBL-positive case, but none of the MBL-negative cases showed glomerular co-deposition of L-ficolin, MBL-associated serine proteases, and C4d. Glomerular deposition of MBL and L-ficolin was associated with more pronounced histologic damage, as evidenced by increased mesangial proliferation, extracapillary proliferation, glomerular sclerosis, and interstitial infiltration, as well as with significantly more proteinuria. Patients who had IgAN with or without glomerular MBL deposition did not show significant differences in serum levels of MBL, L-ficolin, or IgA or in the size distribution of circulating IgA. Furthermore, in vitro experiments showed clear binding of MBL to polymeric but not monomeric patient IgA, without a significant difference between both groups. Together, these findings strongly point to a role for the lectin pathway of complement in glomerular complement activation in IgAN and suggest a contribution for both MBL and L-ficolin in the progression of the disease.
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                Author and article information

                Contributors
                Role: ConceptualizationRole: Data CurationRole: Formal AnalysisRole: Funding AcquisitionRole: InvestigationRole: MethodologyRole: Project AdministrationRole: ResourcesRole: SoftwareRole: Writing – Original Draft PreparationRole: Writing – Review & Editing
                Role: ConceptualizationRole: SupervisionRole: ValidationRole: Writing – Review & Editing
                Role: InvestigationRole: Methodology
                Role: Methodology
                Role: InvestigationRole: Methodology
                Role: InvestigationRole: Methodology
                Role: InvestigationRole: Methodology
                Role: InvestigationRole: Methodology
                Role: InvestigationRole: Methodology
                Role: InvestigationRole: Methodology
                Role: InvestigationRole: Methodology
                Role: Investigation
                Role: Formal AnalysisRole: ValidationRole: Writing – Review & Editing
                Role: InvestigationRole: MethodologyRole: Writing – Review & Editing
                Role: MethodologyRole: ValidationRole: Writing – Review & Editing
                Role: MethodologyRole: ValidationRole: Writing – Review & Editing
                Role: MethodologyRole: SupervisionRole: ValidationRole: Writing – Review & Editing
                Role: MethodologyRole: SupervisionRole: ValidationRole: Writing – Review & Editing
                Role: ConceptualizationRole: MethodologyRole: ResourcesRole: SupervisionRole: ValidationRole: Writing – Review & Editing
                Role: ConceptualizationRole: MethodologyRole: Project AdministrationRole: ResourcesRole: SupervisionRole: ValidationRole: Writing – Review & Editing
                Journal
                Wellcome Open Res
                Wellcome Open Res
                Wellcome Open Res
                Wellcome Open Research
                F1000 Research Limited (London, UK )
                2398-502X
                26 July 2018
                2018
                : 3
                : 91
                Affiliations
                [1 ]Department of Nephrology, Christian Medical College, Vellore, Tamil Nadu, 632004, India
                [2 ]Department of Renal Medicine, Royal Brisbane and Women's Hospital, Queensland, 4029, Australia
                [3 ]Department of General Pathology, Christian Medical College, Vellore, Tamil Nadu, 632004, India
                [4 ]Central Electron Microscope Unit, Christian Medical College, Vellore, Tamil Nadu, 632004, India
                [5 ]Department of Biostatistics, Christian Medical College, Vellore, Tamil Nadu, 632004, India
                [6 ]Centre for Cellular and Molecular Platforms, Bengaluru, Karnataka, 560065, India
                [7 ]Centre for Complement and Inflammation Research, Imperial College, London, UK
                [8 ]Department of Medicine, Imperial College Healthcare NHS Trust, London, UK
                [9 ]Rijksuniversiteit Groningen Faculteit Biologie, Groningen, Netherlands
                [10 ]University of Leicester, College of Medicine Biological Sciences and Psychology, Leicester, UK
                [1 ]The Glasgow Renal and Transplant Unit, Queen Elizabeth University Hospital, Glasgow, UK
                [2 ]University of Glasgow, Glasgow, UK
                [1 ]INSERM 1149, Center of Research on Inflammation, Paris, France
                [2 ]Nephrology unit, St Louis Hospital, Paris, France
                Author notes

                No competing interests were disclosed.

                Competing interests: My institution has received grant funding from Retrophin Inc for research in glomerular diseases.

                Competing interests: No competing interests were disclosed.

                Author information
                https://orcid.org/0000-0001-7692-606X
                https://orcid.org/0000-0002-5268-987X
                https://orcid.org/0000-0002-9063-7229
                Article
                10.12688/wellcomeopenres.14644.1
                6148466
                30345379
                f0406731-41e1-43fb-a018-3479a04cecf4
                Copyright: © 2018 Alexander S et al.

                This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 18 July 2018
                Funding
                Funded by: DBT India Alliance
                Award ID: 501501
                Funded by: Christian Medical College, Vellore
                Award ID: 8962
                This work is supported by the Wellcome Trust/DBT India Alliance Fellowship (grant number 501501). S.A. is a Wellcome Trust/DBT India Alliance Early Career Fellow (Clinical and Public Health). Initial small funding was by a major fluid research internal grant [8962 (Other) dated 23.07.2014] from Christian Medical College, Vellore-632004, India.
                The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Study Protocol
                Articles

                immunology,nephrology,iga nephropathy,glomerulonephritis,pathology,south-asians,indians,epidemiology,protocol

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