Towards a simplified renal histopathological prognostic score in glomerular nephropathies
Aims An important role of native kidney biopsy evaluation is to predict renal prognosis. We aimed to develop a simplified chronicity score based solely on pathological features that are easily recognisable and can be found in all glomerular nephropathies (GN). In this retrospective study, observatio...
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Veröffentlicht in: | Histopathology 2020-12, Vol.77 (6), p.926-935 |
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creator | Stefan, Gabriel Stancu, Simona Zugravu, Adrian Petre, Nicoleta Mandache, Eugen Mircescu, Gabriel |
description | Aims
An important role of native kidney biopsy evaluation is to predict renal prognosis. We aimed to develop a simplified chronicity score based solely on pathological features that are easily recognisable and can be found in all glomerular nephropathies (GN). In this retrospective study, observational cohort study we included 625 patients with GN diagnosis after native kidney biopsy in a tertiary unit between 1 January 2010 and 31 December 2015.
Methods and results
Presence of global glomerulosclerosis (GG), tubular atrophy (TA), interstitial fibrosis (IF) and fibrocellular/fibrous crescents (FC) in any grade was scored with one point; a final score was between 0 and 4 (i.e. ‘absent’ 0 score, ‘moderate’ 1–2 score, ‘severe’ 3–4 score). The primary endpoint was renal replacement therapy (RRT) initiation. Mean baseline estimated glomerular filtration rate (eGFR) was 55.9 ± 29.6 ml/min; during the follow‐up (median = 27 months), 78 patients started RRT. The total mean renal survival time was 60.1 (58.0–62.1) months. GG (41%) was the most frequent lesion, followed by IF (25%), TA (18%) and FC (17%). Patients with absent (65.7; 63.6–67.8 months) chronicity had better renal survival than those with moderate (59.1; 56.1–62.2 months) or severe (42.7; 35.6–49.7 months) chronicity. The score was associated with renal survival [hazard ratio (HR) = 1.33; 1.08–1.64)] independently of the classical prognostic factors. Patients with moderate and severe chronicity had a two‐ and threefold increase in risk of RRT initiation.
Conclusion
Our score was correlated with renal survival independently of the traditional risk factors, and could improve outcome prediction in patients with GN by reducing the interobserver variability. |
doi_str_mv | 10.1111/his.14175 |
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An important role of native kidney biopsy evaluation is to predict renal prognosis. We aimed to develop a simplified chronicity score based solely on pathological features that are easily recognisable and can be found in all glomerular nephropathies (GN). In this retrospective study, observational cohort study we included 625 patients with GN diagnosis after native kidney biopsy in a tertiary unit between 1 January 2010 and 31 December 2015.
Methods and results
Presence of global glomerulosclerosis (GG), tubular atrophy (TA), interstitial fibrosis (IF) and fibrocellular/fibrous crescents (FC) in any grade was scored with one point; a final score was between 0 and 4 (i.e. ‘absent’ 0 score, ‘moderate’ 1–2 score, ‘severe’ 3–4 score). The primary endpoint was renal replacement therapy (RRT) initiation. Mean baseline estimated glomerular filtration rate (eGFR) was 55.9 ± 29.6 ml/min; during the follow‐up (median = 27 months), 78 patients started RRT. The total mean renal survival time was 60.1 (58.0–62.1) months. GG (41%) was the most frequent lesion, followed by IF (25%), TA (18%) and FC (17%). Patients with absent (65.7; 63.6–67.8 months) chronicity had better renal survival than those with moderate (59.1; 56.1–62.2 months) or severe (42.7; 35.6–49.7 months) chronicity. The score was associated with renal survival [hazard ratio (HR) = 1.33; 1.08–1.64)] independently of the classical prognostic factors. Patients with moderate and severe chronicity had a two‐ and threefold increase in risk of RRT initiation.
Conclusion
Our score was correlated with renal survival independently of the traditional risk factors, and could improve outcome prediction in patients with GN by reducing the interobserver variability.</description><identifier>ISSN: 0309-0167</identifier><identifier>EISSN: 1365-2559</identifier><identifier>DOI: 10.1111/his.14175</identifier><language>eng</language><publisher>Oxford: Wiley Subscription Services, Inc</publisher><subject>Atrophy ; Biopsy ; chronic renal failure ; Epidermal growth factor receptors ; Fibrosis ; Glomerular filtration rate ; glomerular nephropathies ; histopathological prognostic score ; Kidneys ; Medical prognosis ; renal biopsy ; renal replacement therapy ; Risk factors ; Survival</subject><ispartof>Histopathology, 2020-12, Vol.77 (6), p.926-935</ispartof><rights>2020 John Wiley & Sons Ltd</rights><rights>Copyright © 2020 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3305-505ac22a399ac54cd71766d95c4d1be52ab42307541cfaa4b244e777f867e5313</citedby><cites>FETCH-LOGICAL-c3305-505ac22a399ac54cd71766d95c4d1be52ab42307541cfaa4b244e777f867e5313</cites><orcidid>0000-0002-7336-5874</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fhis.14175$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fhis.14175$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27915,27916,45565,45566</link.rule.ids></links><search><creatorcontrib>Stefan, Gabriel</creatorcontrib><creatorcontrib>Stancu, Simona</creatorcontrib><creatorcontrib>Zugravu, Adrian</creatorcontrib><creatorcontrib>Petre, Nicoleta</creatorcontrib><creatorcontrib>Mandache, Eugen</creatorcontrib><creatorcontrib>Mircescu, Gabriel</creatorcontrib><title>Towards a simplified renal histopathological prognostic score in glomerular nephropathies</title><title>Histopathology</title><description>Aims
An important role of native kidney biopsy evaluation is to predict renal prognosis. We aimed to develop a simplified chronicity score based solely on pathological features that are easily recognisable and can be found in all glomerular nephropathies (GN). In this retrospective study, observational cohort study we included 625 patients with GN diagnosis after native kidney biopsy in a tertiary unit between 1 January 2010 and 31 December 2015.
Methods and results
Presence of global glomerulosclerosis (GG), tubular atrophy (TA), interstitial fibrosis (IF) and fibrocellular/fibrous crescents (FC) in any grade was scored with one point; a final score was between 0 and 4 (i.e. ‘absent’ 0 score, ‘moderate’ 1–2 score, ‘severe’ 3–4 score). The primary endpoint was renal replacement therapy (RRT) initiation. Mean baseline estimated glomerular filtration rate (eGFR) was 55.9 ± 29.6 ml/min; during the follow‐up (median = 27 months), 78 patients started RRT. The total mean renal survival time was 60.1 (58.0–62.1) months. GG (41%) was the most frequent lesion, followed by IF (25%), TA (18%) and FC (17%). Patients with absent (65.7; 63.6–67.8 months) chronicity had better renal survival than those with moderate (59.1; 56.1–62.2 months) or severe (42.7; 35.6–49.7 months) chronicity. The score was associated with renal survival [hazard ratio (HR) = 1.33; 1.08–1.64)] independently of the classical prognostic factors. Patients with moderate and severe chronicity had a two‐ and threefold increase in risk of RRT initiation.
Conclusion
Our score was correlated with renal survival independently of the traditional risk factors, and could improve outcome prediction in patients with GN by reducing the interobserver variability.</description><subject>Atrophy</subject><subject>Biopsy</subject><subject>chronic renal failure</subject><subject>Epidermal growth factor receptors</subject><subject>Fibrosis</subject><subject>Glomerular filtration rate</subject><subject>glomerular nephropathies</subject><subject>histopathological prognostic score</subject><subject>Kidneys</subject><subject>Medical prognosis</subject><subject>renal biopsy</subject><subject>renal replacement therapy</subject><subject>Risk factors</subject><subject>Survival</subject><issn>0309-0167</issn><issn>1365-2559</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp10M9LwzAUB_AgCs7pwf8g4EUP3fLrNetRhrrBwIPz4KlkabplpE1NWsb-e7vVk2AuD8LnPd77InRPyYT2b7qzcUIFlXCBRpSnkDCA7BKNCCdZQmgqr9FNjHtCqOSMjdDX2h9UKCJWONqqcba0psDB1MrhflbrG9XuvPNbq_ufJvht7WNrNY7aB4NtjbfOVyZ0TgVcm2YXzh3WxFt0VSoXzd1vHaPP15f1fJGs3t-W8-dVojknkAABpRlTPMuUBqELSWWaFhloUdCNAaY2gnEiQVBdKiU2TAgjpSxnqTTAKR-jx2Fuv9x3Z2KbVzZq45yqje9izgSlIADgRB_-0L3vQn_qSaUEZoIQ0aunQengYwymzJtgKxWOOSX5KeS8DyY_h9zb6WAP1pnj_zBfLD-Gjh924H5Q</recordid><startdate>202012</startdate><enddate>202012</enddate><creator>Stefan, Gabriel</creator><creator>Stancu, Simona</creator><creator>Zugravu, Adrian</creator><creator>Petre, Nicoleta</creator><creator>Mandache, Eugen</creator><creator>Mircescu, Gabriel</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7336-5874</orcidid></search><sort><creationdate>202012</creationdate><title>Towards a simplified renal histopathological prognostic score in glomerular nephropathies</title><author>Stefan, Gabriel ; Stancu, Simona ; Zugravu, Adrian ; Petre, Nicoleta ; Mandache, Eugen ; Mircescu, Gabriel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3305-505ac22a399ac54cd71766d95c4d1be52ab42307541cfaa4b244e777f867e5313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Atrophy</topic><topic>Biopsy</topic><topic>chronic renal failure</topic><topic>Epidermal growth factor receptors</topic><topic>Fibrosis</topic><topic>Glomerular filtration rate</topic><topic>glomerular nephropathies</topic><topic>histopathological prognostic score</topic><topic>Kidneys</topic><topic>Medical prognosis</topic><topic>renal biopsy</topic><topic>renal replacement therapy</topic><topic>Risk factors</topic><topic>Survival</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stefan, Gabriel</creatorcontrib><creatorcontrib>Stancu, Simona</creatorcontrib><creatorcontrib>Zugravu, Adrian</creatorcontrib><creatorcontrib>Petre, Nicoleta</creatorcontrib><creatorcontrib>Mandache, Eugen</creatorcontrib><creatorcontrib>Mircescu, Gabriel</creatorcontrib><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Histopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stefan, Gabriel</au><au>Stancu, Simona</au><au>Zugravu, Adrian</au><au>Petre, Nicoleta</au><au>Mandache, Eugen</au><au>Mircescu, Gabriel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Towards a simplified renal histopathological prognostic score in glomerular nephropathies</atitle><jtitle>Histopathology</jtitle><date>2020-12</date><risdate>2020</risdate><volume>77</volume><issue>6</issue><spage>926</spage><epage>935</epage><pages>926-935</pages><issn>0309-0167</issn><eissn>1365-2559</eissn><abstract>Aims
An important role of native kidney biopsy evaluation is to predict renal prognosis. We aimed to develop a simplified chronicity score based solely on pathological features that are easily recognisable and can be found in all glomerular nephropathies (GN). In this retrospective study, observational cohort study we included 625 patients with GN diagnosis after native kidney biopsy in a tertiary unit between 1 January 2010 and 31 December 2015.
Methods and results
Presence of global glomerulosclerosis (GG), tubular atrophy (TA), interstitial fibrosis (IF) and fibrocellular/fibrous crescents (FC) in any grade was scored with one point; a final score was between 0 and 4 (i.e. ‘absent’ 0 score, ‘moderate’ 1–2 score, ‘severe’ 3–4 score). The primary endpoint was renal replacement therapy (RRT) initiation. Mean baseline estimated glomerular filtration rate (eGFR) was 55.9 ± 29.6 ml/min; during the follow‐up (median = 27 months), 78 patients started RRT. The total mean renal survival time was 60.1 (58.0–62.1) months. GG (41%) was the most frequent lesion, followed by IF (25%), TA (18%) and FC (17%). Patients with absent (65.7; 63.6–67.8 months) chronicity had better renal survival than those with moderate (59.1; 56.1–62.2 months) or severe (42.7; 35.6–49.7 months) chronicity. The score was associated with renal survival [hazard ratio (HR) = 1.33; 1.08–1.64)] independently of the classical prognostic factors. Patients with moderate and severe chronicity had a two‐ and threefold increase in risk of RRT initiation.
Conclusion
Our score was correlated with renal survival independently of the traditional risk factors, and could improve outcome prediction in patients with GN by reducing the interobserver variability.</abstract><cop>Oxford</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1111/his.14175</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-7336-5874</orcidid></addata></record> |
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subjects | Atrophy Biopsy chronic renal failure Epidermal growth factor receptors Fibrosis Glomerular filtration rate glomerular nephropathies histopathological prognostic score Kidneys Medical prognosis renal biopsy renal replacement therapy Risk factors Survival |
title | Towards a simplified renal histopathological prognostic score in glomerular nephropathies |
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