Mechanisms of Injury in APOL1-associated Kidney Disease. Issue 3 (March 2019)
- Record Type:
- Journal Article
- Title:
- Mechanisms of Injury in APOL1-associated Kidney Disease. Issue 3 (March 2019)
- Main Title:
- Mechanisms of Injury in APOL1-associated Kidney Disease
- Authors:
- Ma, Lijun
Divers, Jasmin
Freedman, Barry I. - Abstract:
- Abstract : Background: An improved understanding of the pathogenesis in apolipoprotein L1 ( APOL1 ) gene–associated chronic kidney disease (CKD) arose from observations in kidney transplantation. APOL1 genotyping could soon improve the safety of living kidney donation in individuals with recent African ancestry and alter the allocation of deceased donor kidneys. Methods: This article reviews the potential mechanisms that underlie development of APOL1 -associated nephropathy. Roles for circulating APOL1 protein versus intrinsic renal expression of APOL1 are discussed, as well as the requirement for modifying genetic and/or environmental factors. Results: Abundant evidence supports local kidney production of APOL1 renal-risk variant protein in the development of nephropathy; this is true in both native kidney disease and after renal transplantation. Only a minority of kidneys from individuals with APOL1 high-risk genotypes will develop CKD or manifest shorter renal allograft survival after transplantation. Therefore, modifying factors that explain why only a subset of kidneys develops nephropathy remain critical to identify. It appears likely that environmental exposures, as opposed to major APOL1 -second gene interactions, will prove to be stronger modifiers of the risk for nephropathy. Conclusions: The evolving understanding of the pathogenesis in APOL1 -associated nephropathy will identify biomarkers predicting nephropathy in individuals at high genetic risk and lead toAbstract : Background: An improved understanding of the pathogenesis in apolipoprotein L1 ( APOL1 ) gene–associated chronic kidney disease (CKD) arose from observations in kidney transplantation. APOL1 genotyping could soon improve the safety of living kidney donation in individuals with recent African ancestry and alter the allocation of deceased donor kidneys. Methods: This article reviews the potential mechanisms that underlie development of APOL1 -associated nephropathy. Roles for circulating APOL1 protein versus intrinsic renal expression of APOL1 are discussed, as well as the requirement for modifying genetic and/or environmental factors. Results: Abundant evidence supports local kidney production of APOL1 renal-risk variant protein in the development of nephropathy; this is true in both native kidney disease and after renal transplantation. Only a minority of kidneys from individuals with APOL1 high-risk genotypes will develop CKD or manifest shorter renal allograft survival after transplantation. Therefore, modifying factors that explain why only a subset of kidneys develops nephropathy remain critical to identify. It appears likely that environmental exposures, as opposed to major APOL1 -second gene interactions, will prove to be stronger modifiers of the risk for nephropathy. Conclusions: The evolving understanding of the pathogenesis in APOL1 -associated nephropathy will identify biomarkers predicting nephropathy in individuals at high genetic risk and lead to novel therapies to prevent or slow native CKD progression and prolong survival of transplanted kidneys. In the interim, the National Institutes of Health–sponsored " APOL1 Long-term Kidney Transplantation Outcomes" Network will determine whether APOL1 genotyping in individuals with recent African ancestry improves outcomes and safety in kidney transplantation. … (more)
- Is Part Of:
- Transplantation. Volume 103:Issue 3(2019)
- Journal:
- Transplantation
- Issue:
- Volume 103:Issue 3(2019)
- Issue Display:
- Volume 103, Issue 3 (2019)
- Year:
- 2019
- Volume:
- 103
- Issue:
- 3
- Issue Sort Value:
- 2019-0103-0003-0000
- Page Start:
- Page End:
- Publication Date:
- 2019-03
- Subjects:
- Transplantation of organs, tissues, etc -- Periodicals
Transplantation immunology -- Periodicals
617.95 - Journal URLs:
- http://journals.lww.com/pages/default.aspx ↗
- DOI:
- 10.1097/TP.0000000000002509 ↗
- Languages:
- English
- ISSNs:
- 0041-1337
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9024.990000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11735.xml