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PLA2R antibody, PLA2R rs4664308 polymorphism and PLA2R mRNA levels in Tunisian patients with primary membranous nephritis

BACKGROUND: Primary membranous nephritis (PMN) is an autoimmune disease induced by the deposit of antibodies (Ab) to the phospholipase receptor A2 receptor (PLA2R) on podocytes. In this context, we aimed to assess the relationships between anti-PLA2R Ab, PLA2R rs4664308 SNP, PLA2R mRNA levels and PM...

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Autores principales: Dhaouadi, Tarak, Abdellatif, Jihen, Trabelsi, Raja, Gaied, Hanene, Chamkhi, Sameh, Sfar, Imen, Goucha, Rym, Ben Hamida, Fethi, Ben Abdallah, Taieb, Gorgi, Yousr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529277/
https://www.ncbi.nlm.nih.gov/pubmed/33002091
http://dx.doi.org/10.1371/journal.pone.0240025
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author Dhaouadi, Tarak
Abdellatif, Jihen
Trabelsi, Raja
Gaied, Hanene
Chamkhi, Sameh
Sfar, Imen
Goucha, Rym
Ben Hamida, Fethi
Ben Abdallah, Taieb
Gorgi, Yousr
author_facet Dhaouadi, Tarak
Abdellatif, Jihen
Trabelsi, Raja
Gaied, Hanene
Chamkhi, Sameh
Sfar, Imen
Goucha, Rym
Ben Hamida, Fethi
Ben Abdallah, Taieb
Gorgi, Yousr
author_sort Dhaouadi, Tarak
collection PubMed
description BACKGROUND: Primary membranous nephritis (PMN) is an autoimmune disease induced by the deposit of antibodies (Ab) to the phospholipase receptor A2 receptor (PLA2R) on podocytes. In this context, we aimed to assess the relationships between anti-PLA2R Ab, PLA2R rs4664308 SNP, PLA2R mRNA levels and PMN susceptibility and outcome. METHODS: Sixty-eight PMN patients, 30 systemic lupus erythematosus (SLE) patients with secondary MN and 30 healthy control subjects served for anti-PLA2R Ab measurement by ELISA and PLA2R rs4664308 SNP genotyping by a commercial real-time PCR. Twenty patients with tubulo-interstitial nephritis (TIN) were used as controls for renal PLA2R mRNA quantification in PMN patients from kidney biopsies. PLA2R mRNA quantification was carried-out by real-time PCR after RNA extraction. RESULTS: Forty-three (63.2%) PMN patients received initial therapy consisting of alternating monthly cycles of corticosteroids and cyclophosphamide. Twelve (17.6%) patients had resistant PMN to initial therapy and were consecutively treated by cyclosporine or tacrolimus. Anti-PLA2R Ab were positive in 54 (79.4%) PMN patients, while all SLE patients and controls were negative, p<0.0001. Moreover, anti-PLA2R Ab levels were significantly higher in PMN patients (134.85 [41.25–256.97] RU/ml) than in SLE patients (3.35 [2.3–4.35] RU/ml) and controls (2 [2–2.3]), p<0.0001. Consequently, a ROC curve showed for 100% specificity a sensitivity of 94.1% at a threshold of 2.6 RU/ml. Besides, Anti-PLA2R antibodies levels were significantly associated to non-remission; p = 0.002. The rs4664308*A wild-type allele was significantly more frequent in PMN patients (0.809) than in controls (0.633) and SLE patients (0.65); p = 0.008, OR [95% CI] = 2.44 [1.24–4.82] and p = 0.016, OR [95% CI] = 2.27 [1.15–4.5], respectively. Renal PLA2R mRNA levels were significantly higher in PMN patients (218.29 [66.05–486.07]) than in TIN patients (22.09 [13.62–43.34]), p<0.0001. Moreover, PLA2R mRNA levels were significantly higher in non-remission patients (fold-factor vs. partial remission = 2.46 and fold-factor vs. complete remission = 12.25); p = 1.56 10E-8. In addition, PLA2R mRNA and anti-PLA2R Ab levels were significantly correlated, Spearman Rho = 0.958, p<0.0001. CONCLUSION: Anti-PLA2R Ab and renal PLA2R mRNA could be useful markers for PMN outcome predicting. The PLA2R rs6446308 SNP is associated with PMN susceptibility in Tunisians.
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spelling pubmed-75292772020-10-08 PLA2R antibody, PLA2R rs4664308 polymorphism and PLA2R mRNA levels in Tunisian patients with primary membranous nephritis Dhaouadi, Tarak Abdellatif, Jihen Trabelsi, Raja Gaied, Hanene Chamkhi, Sameh Sfar, Imen Goucha, Rym Ben Hamida, Fethi Ben Abdallah, Taieb Gorgi, Yousr PLoS One Research Article BACKGROUND: Primary membranous nephritis (PMN) is an autoimmune disease induced by the deposit of antibodies (Ab) to the phospholipase receptor A2 receptor (PLA2R) on podocytes. In this context, we aimed to assess the relationships between anti-PLA2R Ab, PLA2R rs4664308 SNP, PLA2R mRNA levels and PMN susceptibility and outcome. METHODS: Sixty-eight PMN patients, 30 systemic lupus erythematosus (SLE) patients with secondary MN and 30 healthy control subjects served for anti-PLA2R Ab measurement by ELISA and PLA2R rs4664308 SNP genotyping by a commercial real-time PCR. Twenty patients with tubulo-interstitial nephritis (TIN) were used as controls for renal PLA2R mRNA quantification in PMN patients from kidney biopsies. PLA2R mRNA quantification was carried-out by real-time PCR after RNA extraction. RESULTS: Forty-three (63.2%) PMN patients received initial therapy consisting of alternating monthly cycles of corticosteroids and cyclophosphamide. Twelve (17.6%) patients had resistant PMN to initial therapy and were consecutively treated by cyclosporine or tacrolimus. Anti-PLA2R Ab were positive in 54 (79.4%) PMN patients, while all SLE patients and controls were negative, p<0.0001. Moreover, anti-PLA2R Ab levels were significantly higher in PMN patients (134.85 [41.25–256.97] RU/ml) than in SLE patients (3.35 [2.3–4.35] RU/ml) and controls (2 [2–2.3]), p<0.0001. Consequently, a ROC curve showed for 100% specificity a sensitivity of 94.1% at a threshold of 2.6 RU/ml. Besides, Anti-PLA2R antibodies levels were significantly associated to non-remission; p = 0.002. The rs4664308*A wild-type allele was significantly more frequent in PMN patients (0.809) than in controls (0.633) and SLE patients (0.65); p = 0.008, OR [95% CI] = 2.44 [1.24–4.82] and p = 0.016, OR [95% CI] = 2.27 [1.15–4.5], respectively. Renal PLA2R mRNA levels were significantly higher in PMN patients (218.29 [66.05–486.07]) than in TIN patients (22.09 [13.62–43.34]), p<0.0001. Moreover, PLA2R mRNA levels were significantly higher in non-remission patients (fold-factor vs. partial remission = 2.46 and fold-factor vs. complete remission = 12.25); p = 1.56 10E-8. In addition, PLA2R mRNA and anti-PLA2R Ab levels were significantly correlated, Spearman Rho = 0.958, p<0.0001. CONCLUSION: Anti-PLA2R Ab and renal PLA2R mRNA could be useful markers for PMN outcome predicting. The PLA2R rs6446308 SNP is associated with PMN susceptibility in Tunisians. Public Library of Science 2020-10-01 /pmc/articles/PMC7529277/ /pubmed/33002091 http://dx.doi.org/10.1371/journal.pone.0240025 Text en © 2020 Dhaouadi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dhaouadi, Tarak
Abdellatif, Jihen
Trabelsi, Raja
Gaied, Hanene
Chamkhi, Sameh
Sfar, Imen
Goucha, Rym
Ben Hamida, Fethi
Ben Abdallah, Taieb
Gorgi, Yousr
PLA2R antibody, PLA2R rs4664308 polymorphism and PLA2R mRNA levels in Tunisian patients with primary membranous nephritis
title PLA2R antibody, PLA2R rs4664308 polymorphism and PLA2R mRNA levels in Tunisian patients with primary membranous nephritis
title_full PLA2R antibody, PLA2R rs4664308 polymorphism and PLA2R mRNA levels in Tunisian patients with primary membranous nephritis
title_fullStr PLA2R antibody, PLA2R rs4664308 polymorphism and PLA2R mRNA levels in Tunisian patients with primary membranous nephritis
title_full_unstemmed PLA2R antibody, PLA2R rs4664308 polymorphism and PLA2R mRNA levels in Tunisian patients with primary membranous nephritis
title_short PLA2R antibody, PLA2R rs4664308 polymorphism and PLA2R mRNA levels in Tunisian patients with primary membranous nephritis
title_sort pla2r antibody, pla2r rs4664308 polymorphism and pla2r mrna levels in tunisian patients with primary membranous nephritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529277/
https://www.ncbi.nlm.nih.gov/pubmed/33002091
http://dx.doi.org/10.1371/journal.pone.0240025
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