Oxalate nephropathy in systemic sclerosis: Case series and review of the literature

Abstract Objective To increase awareness of oxalate nephropathy as a cause of acute kidney injury (AKI) among systemic sclerosis patients with small intestinal dysmotility and malabsorption, and to prompt consideration of dietary modification and early treatment of predisposing causes of oxalate nep...

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Veröffentlicht in:Seminars in arthritis and rheumatism 2015-12, Vol.45 (3), p.315-320
Hauptverfasser: Ligon, Colin B., MD, Hummers, Laura K., MD, ScM, McMahan, Zsuzsanna H., MD, MHS
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creator Ligon, Colin B., MD
Hummers, Laura K., MD, ScM
McMahan, Zsuzsanna H., MD, MHS
description Abstract Objective To increase awareness of oxalate nephropathy as a cause of acute kidney injury (AKI) among systemic sclerosis patients with small intestinal dysmotility and malabsorption, and to prompt consideration of dietary modification and early treatment of predisposing causes of oxalate nephropathy in this population. Methods Two cases of biopsy-proven oxalate nephropathy were identified among systemic sclerosis patients in the course of direct clinical care. Subsequently, a retrospective search of the Johns Hopkins Pathology databases identified a third patient with systemic sclerosis who developed oxalate nephropathy. Results Among the three patients with qualifying biopsies, all three had systemic sclerosis with lower gastrointestinal involvement. All three presented with diarrhea, malabsorption, and AKI. In two of the three patients, diarrhea was present for at least 2 years before the development of AKI; in the third, incidental oxalate nephropathy was noted 3 years before she developed AKI and extensive oxalate nephropathy in the setting of a prolonged mycobacterium avium-intracellulare enteritis. In the first case, oxalate crystals were present by urinalysis months before diagnosis by biopsy; in the second, hyperoxaluria was diagnosed by urine collection immediately after; and in the third, oxalate crystals had been noted incidentally on post-transplant renal biopsy 3 years before the development of fulminant oxalate nephropathy. All three patients died within a year after diagnosis. Conclusions Patients with systemic sclerosis and bowel dysmotility associated with chronic diarrhea and malabsorption may be at risk for an associated oxalate nephropathy. Regular screening of systemic sclerosis patients with small bowel malabsorption syndromes through routine urinalysis or 24-h urine oxalate collection, should be considered. Further studies defining the prevalence of this complication in systemic sclerosis, the benefit of dietary modification on hyperoxaluria, the effect of treating small intestinal bowel overgrowth with antibiotics, and the effectiveness of probiotics, calcium supplements, or magnesium supplements to prevent hyperoxaluria-associated renal disease in these patients, are warranted.
doi_str_mv 10.1016/j.semarthrit.2015.06.017
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Methods Two cases of biopsy-proven oxalate nephropathy were identified among systemic sclerosis patients in the course of direct clinical care. Subsequently, a retrospective search of the Johns Hopkins Pathology databases identified a third patient with systemic sclerosis who developed oxalate nephropathy. Results Among the three patients with qualifying biopsies, all three had systemic sclerosis with lower gastrointestinal involvement. All three presented with diarrhea, malabsorption, and AKI. In two of the three patients, diarrhea was present for at least 2 years before the development of AKI; in the third, incidental oxalate nephropathy was noted 3 years before she developed AKI and extensive oxalate nephropathy in the setting of a prolonged mycobacterium avium-intracellulare enteritis. In the first case, oxalate crystals were present by urinalysis months before diagnosis by biopsy; in the second, hyperoxaluria was diagnosed by urine collection immediately after; and in the third, oxalate crystals had been noted incidentally on post-transplant renal biopsy 3 years before the development of fulminant oxalate nephropathy. All three patients died within a year after diagnosis. Conclusions Patients with systemic sclerosis and bowel dysmotility associated with chronic diarrhea and malabsorption may be at risk for an associated oxalate nephropathy. Regular screening of systemic sclerosis patients with small bowel malabsorption syndromes through routine urinalysis or 24-h urine oxalate collection, should be considered. Further studies defining the prevalence of this complication in systemic sclerosis, the benefit of dietary modification on hyperoxaluria, the effect of treating small intestinal bowel overgrowth with antibiotics, and the effectiveness of probiotics, calcium supplements, or magnesium supplements to prevent hyperoxaluria-associated renal disease in these patients, are warranted.</description><identifier>ISSN: 0049-0172</identifier><identifier>EISSN: 1532-866X</identifier><identifier>DOI: 10.1016/j.semarthrit.2015.06.017</identifier><identifier>PMID: 26239907</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Acute kidney injury ; Acute Kidney Injury - complications ; Acute Kidney Injury - urine ; Aged ; Calcium oxalate ; Chronic kidney disease ; Female ; Gastrointestinal disease ; Humans ; Hyperoxaluria - complications ; Hyperoxaluria - urine ; Malabsorption ; Middle Aged ; Oxalate nephropathy ; Oxalic Acid - urine ; Rheumatology ; Scleroderma ; Scleroderma renal crisis ; Scleroderma, Systemic - complications ; Scleroderma, Systemic - urine ; Small intestinal bacterial overgrowth ; Systemic sclerosis</subject><ispartof>Seminars in arthritis and rheumatism, 2015-12, Vol.45 (3), p.315-320</ispartof><rights>Elsevier Inc.</rights><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c604t-a5c6e1c9b5160dc37537968821cee401c36d047930594c13b3f2abb7fc16cac03</citedby><cites>FETCH-LOGICAL-c604t-a5c6e1c9b5160dc37537968821cee401c36d047930594c13b3f2abb7fc16cac03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0049017215001833$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26239907$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ligon, Colin B., MD</creatorcontrib><creatorcontrib>Hummers, Laura K., MD, ScM</creatorcontrib><creatorcontrib>McMahan, Zsuzsanna H., MD, MHS</creatorcontrib><title>Oxalate nephropathy in systemic sclerosis: Case series and review of the literature</title><title>Seminars in arthritis and rheumatism</title><addtitle>Semin Arthritis Rheum</addtitle><description>Abstract Objective To increase awareness of oxalate nephropathy as a cause of acute kidney injury (AKI) among systemic sclerosis patients with small intestinal dysmotility and malabsorption, and to prompt consideration of dietary modification and early treatment of predisposing causes of oxalate nephropathy in this population. Methods Two cases of biopsy-proven oxalate nephropathy were identified among systemic sclerosis patients in the course of direct clinical care. Subsequently, a retrospective search of the Johns Hopkins Pathology databases identified a third patient with systemic sclerosis who developed oxalate nephropathy. Results Among the three patients with qualifying biopsies, all three had systemic sclerosis with lower gastrointestinal involvement. All three presented with diarrhea, malabsorption, and AKI. In two of the three patients, diarrhea was present for at least 2 years before the development of AKI; in the third, incidental oxalate nephropathy was noted 3 years before she developed AKI and extensive oxalate nephropathy in the setting of a prolonged mycobacterium avium-intracellulare enteritis. In the first case, oxalate crystals were present by urinalysis months before diagnosis by biopsy; in the second, hyperoxaluria was diagnosed by urine collection immediately after; and in the third, oxalate crystals had been noted incidentally on post-transplant renal biopsy 3 years before the development of fulminant oxalate nephropathy. All three patients died within a year after diagnosis. Conclusions Patients with systemic sclerosis and bowel dysmotility associated with chronic diarrhea and malabsorption may be at risk for an associated oxalate nephropathy. Regular screening of systemic sclerosis patients with small bowel malabsorption syndromes through routine urinalysis or 24-h urine oxalate collection, should be considered. Further studies defining the prevalence of this complication in systemic sclerosis, the benefit of dietary modification on hyperoxaluria, the effect of treating small intestinal bowel overgrowth with antibiotics, and the effectiveness of probiotics, calcium supplements, or magnesium supplements to prevent hyperoxaluria-associated renal disease in these patients, are warranted.</description><subject>Acute kidney injury</subject><subject>Acute Kidney Injury - complications</subject><subject>Acute Kidney Injury - urine</subject><subject>Aged</subject><subject>Calcium oxalate</subject><subject>Chronic kidney disease</subject><subject>Female</subject><subject>Gastrointestinal disease</subject><subject>Humans</subject><subject>Hyperoxaluria - complications</subject><subject>Hyperoxaluria - urine</subject><subject>Malabsorption</subject><subject>Middle Aged</subject><subject>Oxalate nephropathy</subject><subject>Oxalic Acid - urine</subject><subject>Rheumatology</subject><subject>Scleroderma</subject><subject>Scleroderma renal crisis</subject><subject>Scleroderma, Systemic - complications</subject><subject>Scleroderma, Systemic - urine</subject><subject>Small intestinal bacterial overgrowth</subject><subject>Systemic sclerosis</subject><issn>0049-0172</issn><issn>1532-866X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk1v1DAQhi0EokvhLyAfuWwYx4mTcKgEK76kSj0UJG4jZzIhXrLJYjst--_xakv5OHGyNH7nndHzjhBSQaZAmZfbLPDO-jh4F7McVJmByUBVD8RKlTpf18Z8eShWAEWzTuX8TDwJYQuglIHqsTjLTa6bBqqVuL76YUcbWU68H_y8t3E4SDfJcAiRd45koJH9HFx4JTc2sAzsHQdpp056vnF8K-dexoHl6CJ7GxfPT8Wj3o6Bn9295-Lzu7efNh_Wl1fvP25eX67JQBHXtiTDipq2TFt1pKtSV42p61wRcwGKtOmgqBoNZVOQ0q3uc9u2VU_KkCXQ5-Li5Ltf2h13xFP0dsS9d4nNAWfr8O-fyQ34db7BwpQGTJUMXtwZ-Pn7wiHizgXicbQTz0tAVemyUQmaSdL6JKUEI3ju78cowGMmuMXfmeAxEwSDCX5qff7nmveNv0JIgjcnASdYCanHQI4n4s55pojd7P5nysU_JjS6yZEdv_GBw3Ze_JTCQIUhR8Dr420cT0OV6SxqrfVPAZq5xw</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Ligon, Colin B., MD</creator><creator>Hummers, Laura K., MD, ScM</creator><creator>McMahan, Zsuzsanna H., MD, MHS</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151201</creationdate><title>Oxalate nephropathy in systemic sclerosis: Case series and review of the literature</title><author>Ligon, Colin B., MD ; Hummers, Laura K., MD, ScM ; McMahan, Zsuzsanna H., MD, MHS</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c604t-a5c6e1c9b5160dc37537968821cee401c36d047930594c13b3f2abb7fc16cac03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acute kidney injury</topic><topic>Acute Kidney Injury - complications</topic><topic>Acute Kidney Injury - urine</topic><topic>Aged</topic><topic>Calcium oxalate</topic><topic>Chronic kidney disease</topic><topic>Female</topic><topic>Gastrointestinal disease</topic><topic>Humans</topic><topic>Hyperoxaluria - complications</topic><topic>Hyperoxaluria - urine</topic><topic>Malabsorption</topic><topic>Middle Aged</topic><topic>Oxalate nephropathy</topic><topic>Oxalic Acid - urine</topic><topic>Rheumatology</topic><topic>Scleroderma</topic><topic>Scleroderma renal crisis</topic><topic>Scleroderma, Systemic - complications</topic><topic>Scleroderma, Systemic - urine</topic><topic>Small intestinal bacterial overgrowth</topic><topic>Systemic sclerosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ligon, Colin B., MD</creatorcontrib><creatorcontrib>Hummers, Laura K., MD, ScM</creatorcontrib><creatorcontrib>McMahan, Zsuzsanna H., MD, MHS</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Seminars in arthritis and rheumatism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ligon, Colin B., MD</au><au>Hummers, Laura K., MD, ScM</au><au>McMahan, Zsuzsanna H., MD, MHS</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oxalate nephropathy in systemic sclerosis: Case series and review of the literature</atitle><jtitle>Seminars in arthritis and rheumatism</jtitle><addtitle>Semin Arthritis Rheum</addtitle><date>2015-12-01</date><risdate>2015</risdate><volume>45</volume><issue>3</issue><spage>315</spage><epage>320</epage><pages>315-320</pages><issn>0049-0172</issn><eissn>1532-866X</eissn><abstract>Abstract Objective To increase awareness of oxalate nephropathy as a cause of acute kidney injury (AKI) among systemic sclerosis patients with small intestinal dysmotility and malabsorption, and to prompt consideration of dietary modification and early treatment of predisposing causes of oxalate nephropathy in this population. Methods Two cases of biopsy-proven oxalate nephropathy were identified among systemic sclerosis patients in the course of direct clinical care. Subsequently, a retrospective search of the Johns Hopkins Pathology databases identified a third patient with systemic sclerosis who developed oxalate nephropathy. Results Among the three patients with qualifying biopsies, all three had systemic sclerosis with lower gastrointestinal involvement. All three presented with diarrhea, malabsorption, and AKI. In two of the three patients, diarrhea was present for at least 2 years before the development of AKI; in the third, incidental oxalate nephropathy was noted 3 years before she developed AKI and extensive oxalate nephropathy in the setting of a prolonged mycobacterium avium-intracellulare enteritis. In the first case, oxalate crystals were present by urinalysis months before diagnosis by biopsy; in the second, hyperoxaluria was diagnosed by urine collection immediately after; and in the third, oxalate crystals had been noted incidentally on post-transplant renal biopsy 3 years before the development of fulminant oxalate nephropathy. All three patients died within a year after diagnosis. Conclusions Patients with systemic sclerosis and bowel dysmotility associated with chronic diarrhea and malabsorption may be at risk for an associated oxalate nephropathy. Regular screening of systemic sclerosis patients with small bowel malabsorption syndromes through routine urinalysis or 24-h urine oxalate collection, should be considered. Further studies defining the prevalence of this complication in systemic sclerosis, the benefit of dietary modification on hyperoxaluria, the effect of treating small intestinal bowel overgrowth with antibiotics, and the effectiveness of probiotics, calcium supplements, or magnesium supplements to prevent hyperoxaluria-associated renal disease in these patients, are warranted.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26239907</pmid><doi>10.1016/j.semarthrit.2015.06.017</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Acute kidney injury
Acute Kidney Injury - complications
Acute Kidney Injury - urine
Aged
Calcium oxalate
Chronic kidney disease
Female
Gastrointestinal disease
Humans
Hyperoxaluria - complications
Hyperoxaluria - urine
Malabsorption
Middle Aged
Oxalate nephropathy
Oxalic Acid - urine
Rheumatology
Scleroderma
Scleroderma renal crisis
Scleroderma, Systemic - complications
Scleroderma, Systemic - urine
Small intestinal bacterial overgrowth
Systemic sclerosis
title Oxalate nephropathy in systemic sclerosis: Case series and review of the literature
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