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Histological grading in primary membranous nephropathy is essential for clinical management and predicts outcome of patients.
Stangou, Maria J; Marinaki, Smaragdi; Papachristou, Evangelos; Liapis, George; Pateinakis, Panagiotis; Gakiopoulou, Hara; Nikolaidou, Christina; Kolovou, Kyriaki; Lampropoulou, Ioanna-Theologia; Zerbala, Synodi; Papadea, Panagiota; Dounousi, Evangelia; Balafa, Olga; Pavlakou, Paraskevi; Andrikos, Aimilios; Balassi, Eufemia; Manolakaki, Panagiota; Moustakas, George; Galitsiou, Dimitra; Mitsopoulos, Efstathios; Vourlakou, Christina; Choulitoudi, Vasiliki; Andronikidi, Paraskevi-Evi; Stefanidis, Ioannis; Golfinopoulos, Spyridon; Dafnis, Eugene; Stylianou, Kostas; Panagoutsos, Stylianos; Papadogianakis, Apostolos; Tzanakis, Ioannis; Sioulis, Athanasios; Vlahakos, Demetrios; Grapsa, Irene; Tsilivigkou, Maria; Kaperonis, Nikolaos; Paliouras, Christos; Dioudis, Christos; Spaia, Sophia; Apostolou, Theofanis; Iatrou, Christos; Boletis, John; Goumenos, Dimitrios; Papagianni, Aikaterini.
Afiliação
  • Stangou MJ; Hippokration General Hospital, Aristotle University, Thessaloniki, Greece.
  • Marinaki S; National and Kapodistrian University, Laiko General Hospital, Athens, Greece.
  • Papachristou E; University Hospital of Patras, Patras, Greece.
  • Liapis G; National and Kapodistrian University, Laiko General Hospital, Athens, Greece.
  • Pateinakis P; Papageorgiou General Hospital of Thessaloniki, Thessaloniki, Greece.
  • Gakiopoulou H; National and Kapodistrian University, Laiko General Hospital, Athens, Greece.
  • Nikolaidou C; Hippokration General Hospital, Aristotle University, Thessaloniki, Greece.
  • Kolovou K; National and Kapodistrian University, Laiko General Hospital, Athens, Greece.
  • Lampropoulou IT; Hippokration General Hospital, Aristotle University, Thessaloniki, Greece.
  • Zerbala S; General Hospital of Nikaia, Piraeus, Greece.
  • Papadea P; General Hospital of Nikaia, Piraeus, Greece.
  • Dounousi E; University Hospital of Ioannina, Ioannina, Greece.
  • Balafa O; University Hospital of Ioannina, Ioannina, Greece.
  • Pavlakou P; University Hospital of Ioannina, Ioannina, Greece.
  • Andrikos A; Hatzikosta General Hospital of Ioannina, Ioannina, Greece.
  • Balassi E; Hatzikosta General Hospital of Ioannina, Ioannina, Greece.
  • Manolakaki P; Hatzikosta General Hospital of Ioannina, Ioannina, Greece.
  • Moustakas G; Gennimatas General Hospital of Athens, Athens, Greece.
  • Galitsiou D; Gennimatas General Hospital of Athens, Athens, Greece.
  • Mitsopoulos E; Papageorgiou General Hospital of Thessaloniki, Thessaloniki, Greece.
  • Vourlakou C; Evaggelismos General Hospital, Athens, Greece.
  • Choulitoudi V; Evaggelismos General Hospital, Athens, Greece.
  • Andronikidi PE; Evaggelismos General Hospital, Athens, Greece.
  • Stefanidis I; University Hospital of Larissa, Larissa, Greece.
  • Golfinopoulos S; University Hospital of Larissa, Larissa, Greece.
  • Dafnis E; University Hospital of Heraklion, Heraklion, Crete, Greece.
  • Stylianou K; University Hospital of Heraklion, Heraklion, Crete, Greece.
  • Panagoutsos S; University Hospital of Alexandroupolis, Alexandroupoli, Greece.
  • Papadogianakis A; Venizelio General Hospital of Heraklion, Heraklion, Crete, Greece.
  • Tzanakis I; General Hospital of Chania, Chania, Crete, Greece.
  • Sioulis A; AHEPA University General Hospital, Thessaloniki, Greece.
  • Vlahakos D; Attikon University Hospital, National and Kapodistrian University, Athens, Greece.
  • Grapsa I; Aretaieio Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Tsilivigkou M; Tzaneion General Hospital of Piraeus, Athens, Greece.
  • Kaperonis N; Hellenic Red Cross Hospital Korgialeneio-Benakeio, Athens, Greece.
  • Paliouras C; General Hospital of Rhodes, Rhodes, Greece.
  • Dioudis C; General Hospital of Drama, Drama, Greece.
  • Spaia S; General Hospital of Thessaloniki 'Agios Pavlos', Thessaloniki, Greece.
  • Apostolou T; Venizelio General Hospital of Heraklion, Heraklion, Crete, Greece.
  • Iatrou C; General Hospital of Nikaia, Piraeus, Greece.
  • Boletis J; National and Kapodistrian University, Laiko General Hospital, Athens, Greece.
  • Goumenos D; University Hospital of Patras, Patras, Greece.
  • Papagianni A; Hippokration General Hospital, Aristotle University, Thessaloniki, Greece.
Histopathology ; 75(5): 660-671, 2019 Nov.
Article em En | MEDLINE | ID: mdl-31318463
AIMS: Diagnosis of primary membranous nephropathy (PMN) is mainly based on immunofluorescence/immunohistochemistry findings. However, assessment of specific features on optical microscopy can help to estimate the severity of the disease, guide treatment and predict the response. The aim of this study was to identify, classify and grade the precise histological findings in PMN to predict renal function outcome and guide treatment. METHODS AND RESULTS: Histological parameters, including focal segmental sclerosis (FSGS), tubular atrophy (TA), interstitial fibrosis (IF) and vascular hyalinosis (VH), were re-evaluated in 752 patients with PMN. Their predictive value was estimated separately, and also in a combination score (FSTIV) graded from 0 to 4. Finally, the impact of histology was assessed in the response to immunosuppressive treatment. Mean age of patients was 53.3 (15-85) years and most presented with nephrotic syndrome. FSGS was present in 32% and VH in 51% of the patients, while TA and IF were graded as stage ≥1 in 52% and 51.4%, respectively. The follow-up period was 122.3 (112-376) months. FSGS, TA and IF and VH were associated with impaired renal function at diagnosis (P = 0.02, P < 0.0001, P = 0.001 and P = 0.02, respectively) and at the end of follow-up (P = 0.004, P < 0.0001, P < 0.0001 and P = 0.04, respectively). In multiple regression and binary logistic analysis, the presence of FSGS and degree of TA were the most significant parameters predicting renal function outcome, defined either by eGFR (end), FSGS (r = 0.6, P < 0.0001) and TA (r = 0.6, P < 0.0001), or by the endpoint of >50% eGFR reduction, FSGS (P = 0.001) and TA (P = 0.02). Also, patients presented with FSGS, IF, VH and/or with FSTIV > 1 could benefit from immunosuppression, regardless of clinical presentation. CONCLUSIONS: The presence and degree of four histological indices, FSGS, VH, TA and IF, assessed separately or in combination, and FSTIV score not only predict renal function outcome after long-term follow-up, but can also help in the choice of appropriate treatment. Decisions concerning immunosuppressive treatment can be guided by pathology regardless of clinical findings.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glomerulonefrite Membranosa / Rim / Nefropatias Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glomerulonefrite Membranosa / Rim / Nefropatias Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article