Loading…
Underlying Genetics of aHUS: Which Connection with Outcome and Treatment Discontinuation?
Atypical hemolytic uremic syndrome (aHUS) is a rare disease caused by a genetic dysregulation of the alternative complement pathway, characterized by thrombocytopenia, hemolytic anemia, and acute kidney injury, and included in the group of thrombotic microangiopathies. With the introduction of human...
Saved in:
Published in: | International journal of molecular sciences 2023-10, Vol.24 (19), p.14496 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c393t-12bdb22267a9c0eec2b600f021872bbac3ba49b2ea4b976d109ad0a2edb089e63 |
---|---|
cites | cdi_FETCH-LOGICAL-c393t-12bdb22267a9c0eec2b600f021872bbac3ba49b2ea4b976d109ad0a2edb089e63 |
container_end_page | |
container_issue | 19 |
container_start_page | 14496 |
container_title | International journal of molecular sciences |
container_volume | 24 |
creator | Spasiano, Andrea Palazzetti, Daniela Dimartino, Lucrezia Bruno, Francesca Baccaro, Rocco Pesce, Francesco Grandaliano, Giuseppe |
description | Atypical hemolytic uremic syndrome (aHUS) is a rare disease caused by a genetic dysregulation of the alternative complement pathway, characterized by thrombocytopenia, hemolytic anemia, and acute kidney injury, and included in the group of thrombotic microangiopathies. With the introduction of humanized monoclonal antibodies that inhibit C5 activation, the natural history of aHUS completely changed, with a better prognosis, a quick recovery of renal function, and a significant reduction of end-stage renal disease incidence. Nowadays, there is an increasing interest in the molecular and genetic bases of this severe disease. The aim of this narrative review is to provide readers with a practical guide about different possible involved genes, elucidating the specific role of each transcribed protein in the pathogenesis of aHUS. Moreover, we analyzed the main current evidence about the relationship among genetic mutations, outcomes, and the risk of recurrence of this manifold disease. |
doi_str_mv | 10.3390/ijms241914496 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10572301</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2876750436</sourcerecordid><originalsourceid>FETCH-LOGICAL-c393t-12bdb22267a9c0eec2b600f021872bbac3ba49b2ea4b976d109ad0a2edb089e63</originalsourceid><addsrcrecordid>eNpdkUtrHDEQhEVIiB_JMXdBLrmM3XrsaJSLCevYDhh8iJeQk5A0vV4tM5IjaRz232cWG2Pn1A39dVFFEfKJwYkQGk7DdixcMs2k1O0bcsgk5w1Aq96-2A_IUSlbAC74Qr8nB0J187OUh-T3KvaYh12Id_QSI9bgC01raq9WP7_SX5vgN3SZYkRfQ4r0b6gbejNVn0akNvb0NqOtI8ZKz0PxKdYQJ7tHzz6Qd2s7FPz4NI_J6uL77fKqub65_LH8dt14oUVtGHe945y3ymoPiJ67FmANnHWKO2e9cFZqx9FKp1XbM9C2B8uxd9BpbMUxOXvUvZ_ciL2fvWQ7mPscRpt3JtlgXl9i2Ji79GAYLBQXwGaFL08KOf2ZsFQzzllwGGzENBXDO6VEt-iUnNHP_6HbNOU459tTrVqAFHtLzSPlcyol4_rZDQOzb828ak38A26zioE</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2876750436</pqid></control><display><type>article</type><title>Underlying Genetics of aHUS: Which Connection with Outcome and Treatment Discontinuation?</title><source>Publicly Available Content (ProQuest)</source><source>PubMed Central</source><source>Coronavirus Research Database</source><creator>Spasiano, Andrea ; Palazzetti, Daniela ; Dimartino, Lucrezia ; Bruno, Francesca ; Baccaro, Rocco ; Pesce, Francesco ; Grandaliano, Giuseppe</creator><creatorcontrib>Spasiano, Andrea ; Palazzetti, Daniela ; Dimartino, Lucrezia ; Bruno, Francesca ; Baccaro, Rocco ; Pesce, Francesco ; Grandaliano, Giuseppe</creatorcontrib><description>Atypical hemolytic uremic syndrome (aHUS) is a rare disease caused by a genetic dysregulation of the alternative complement pathway, characterized by thrombocytopenia, hemolytic anemia, and acute kidney injury, and included in the group of thrombotic microangiopathies. With the introduction of humanized monoclonal antibodies that inhibit C5 activation, the natural history of aHUS completely changed, with a better prognosis, a quick recovery of renal function, and a significant reduction of end-stage renal disease incidence. Nowadays, there is an increasing interest in the molecular and genetic bases of this severe disease. The aim of this narrative review is to provide readers with a practical guide about different possible involved genes, elucidating the specific role of each transcribed protein in the pathogenesis of aHUS. Moreover, we analyzed the main current evidence about the relationship among genetic mutations, outcomes, and the risk of recurrence of this manifold disease.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms241914496</identifier><identifier>PMID: 37833944</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Antibodies ; Chromosomes ; Genes ; Glycoproteins ; Hypertension ; Immune system ; Influenza ; Kidneys ; Kinases ; Mutation ; Pathogenesis ; Proteins ; Rare diseases ; Review ; Severe acute respiratory syndrome coronavirus 2 ; Streptococcus infections ; Transplants & implants</subject><ispartof>International journal of molecular sciences, 2023-10, Vol.24 (19), p.14496</ispartof><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-12bdb22267a9c0eec2b600f021872bbac3ba49b2ea4b976d109ad0a2edb089e63</citedby><cites>FETCH-LOGICAL-c393t-12bdb22267a9c0eec2b600f021872bbac3ba49b2ea4b976d109ad0a2edb089e63</cites><orcidid>0000-0002-6044-7256</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2876750436/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2876750436?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,38493,43871,44566,53766,53768,74155,74869</link.rule.ids></links><search><creatorcontrib>Spasiano, Andrea</creatorcontrib><creatorcontrib>Palazzetti, Daniela</creatorcontrib><creatorcontrib>Dimartino, Lucrezia</creatorcontrib><creatorcontrib>Bruno, Francesca</creatorcontrib><creatorcontrib>Baccaro, Rocco</creatorcontrib><creatorcontrib>Pesce, Francesco</creatorcontrib><creatorcontrib>Grandaliano, Giuseppe</creatorcontrib><title>Underlying Genetics of aHUS: Which Connection with Outcome and Treatment Discontinuation?</title><title>International journal of molecular sciences</title><description>Atypical hemolytic uremic syndrome (aHUS) is a rare disease caused by a genetic dysregulation of the alternative complement pathway, characterized by thrombocytopenia, hemolytic anemia, and acute kidney injury, and included in the group of thrombotic microangiopathies. With the introduction of humanized monoclonal antibodies that inhibit C5 activation, the natural history of aHUS completely changed, with a better prognosis, a quick recovery of renal function, and a significant reduction of end-stage renal disease incidence. Nowadays, there is an increasing interest in the molecular and genetic bases of this severe disease. The aim of this narrative review is to provide readers with a practical guide about different possible involved genes, elucidating the specific role of each transcribed protein in the pathogenesis of aHUS. Moreover, we analyzed the main current evidence about the relationship among genetic mutations, outcomes, and the risk of recurrence of this manifold disease.</description><subject>Antibodies</subject><subject>Chromosomes</subject><subject>Genes</subject><subject>Glycoproteins</subject><subject>Hypertension</subject><subject>Immune system</subject><subject>Influenza</subject><subject>Kidneys</subject><subject>Kinases</subject><subject>Mutation</subject><subject>Pathogenesis</subject><subject>Proteins</subject><subject>Rare diseases</subject><subject>Review</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Streptococcus infections</subject><subject>Transplants & implants</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><recordid>eNpdkUtrHDEQhEVIiB_JMXdBLrmM3XrsaJSLCevYDhh8iJeQk5A0vV4tM5IjaRz232cWG2Pn1A39dVFFEfKJwYkQGk7DdixcMs2k1O0bcsgk5w1Aq96-2A_IUSlbAC74Qr8nB0J187OUh-T3KvaYh12Id_QSI9bgC01raq9WP7_SX5vgN3SZYkRfQ4r0b6gbejNVn0akNvb0NqOtI8ZKz0PxKdYQJ7tHzz6Qd2s7FPz4NI_J6uL77fKqub65_LH8dt14oUVtGHe945y3ymoPiJ67FmANnHWKO2e9cFZqx9FKp1XbM9C2B8uxd9BpbMUxOXvUvZ_ciL2fvWQ7mPscRpt3JtlgXl9i2Ji79GAYLBQXwGaFL08KOf2ZsFQzzllwGGzENBXDO6VEt-iUnNHP_6HbNOU459tTrVqAFHtLzSPlcyol4_rZDQOzb828ak38A26zioE</recordid><startdate>20231001</startdate><enddate>20231001</enddate><creator>Spasiano, Andrea</creator><creator>Palazzetti, Daniela</creator><creator>Dimartino, Lucrezia</creator><creator>Bruno, Francesca</creator><creator>Baccaro, Rocco</creator><creator>Pesce, Francesco</creator><creator>Grandaliano, Giuseppe</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6044-7256</orcidid></search><sort><creationdate>20231001</creationdate><title>Underlying Genetics of aHUS: Which Connection with Outcome and Treatment Discontinuation?</title><author>Spasiano, Andrea ; Palazzetti, Daniela ; Dimartino, Lucrezia ; Bruno, Francesca ; Baccaro, Rocco ; Pesce, Francesco ; Grandaliano, Giuseppe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-12bdb22267a9c0eec2b600f021872bbac3ba49b2ea4b976d109ad0a2edb089e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antibodies</topic><topic>Chromosomes</topic><topic>Genes</topic><topic>Glycoproteins</topic><topic>Hypertension</topic><topic>Immune system</topic><topic>Influenza</topic><topic>Kidneys</topic><topic>Kinases</topic><topic>Mutation</topic><topic>Pathogenesis</topic><topic>Proteins</topic><topic>Rare diseases</topic><topic>Review</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Streptococcus infections</topic><topic>Transplants & implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spasiano, Andrea</creatorcontrib><creatorcontrib>Palazzetti, Daniela</creatorcontrib><creatorcontrib>Dimartino, Lucrezia</creatorcontrib><creatorcontrib>Bruno, Francesca</creatorcontrib><creatorcontrib>Baccaro, Rocco</creatorcontrib><creatorcontrib>Pesce, Francesco</creatorcontrib><creatorcontrib>Grandaliano, Giuseppe</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Coronavirus Research Database</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Spasiano, Andrea</au><au>Palazzetti, Daniela</au><au>Dimartino, Lucrezia</au><au>Bruno, Francesca</au><au>Baccaro, Rocco</au><au>Pesce, Francesco</au><au>Grandaliano, Giuseppe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Underlying Genetics of aHUS: Which Connection with Outcome and Treatment Discontinuation?</atitle><jtitle>International journal of molecular sciences</jtitle><date>2023-10-01</date><risdate>2023</risdate><volume>24</volume><issue>19</issue><spage>14496</spage><pages>14496-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Atypical hemolytic uremic syndrome (aHUS) is a rare disease caused by a genetic dysregulation of the alternative complement pathway, characterized by thrombocytopenia, hemolytic anemia, and acute kidney injury, and included in the group of thrombotic microangiopathies. With the introduction of humanized monoclonal antibodies that inhibit C5 activation, the natural history of aHUS completely changed, with a better prognosis, a quick recovery of renal function, and a significant reduction of end-stage renal disease incidence. Nowadays, there is an increasing interest in the molecular and genetic bases of this severe disease. The aim of this narrative review is to provide readers with a practical guide about different possible involved genes, elucidating the specific role of each transcribed protein in the pathogenesis of aHUS. Moreover, we analyzed the main current evidence about the relationship among genetic mutations, outcomes, and the risk of recurrence of this manifold disease.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>37833944</pmid><doi>10.3390/ijms241914496</doi><orcidid>https://orcid.org/0000-0002-6044-7256</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1422-0067 |
ispartof | International journal of molecular sciences, 2023-10, Vol.24 (19), p.14496 |
issn | 1422-0067 1661-6596 1422-0067 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10572301 |
source | Publicly Available Content (ProQuest); PubMed Central; Coronavirus Research Database |
subjects | Antibodies Chromosomes Genes Glycoproteins Hypertension Immune system Influenza Kidneys Kinases Mutation Pathogenesis Proteins Rare diseases Review Severe acute respiratory syndrome coronavirus 2 Streptococcus infections Transplants & implants |
title | Underlying Genetics of aHUS: Which Connection with Outcome and Treatment Discontinuation? |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T20%3A49%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Underlying%20Genetics%20of%20aHUS:%20Which%20Connection%20with%20Outcome%20and%20Treatment%20Discontinuation?&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Spasiano,%20Andrea&rft.date=2023-10-01&rft.volume=24&rft.issue=19&rft.spage=14496&rft.pages=14496-&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms241914496&rft_dat=%3Cproquest_pubme%3E2876750436%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c393t-12bdb22267a9c0eec2b600f021872bbac3ba49b2ea4b976d109ad0a2edb089e63%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2876750436&rft_id=info:pmid/37833944&rfr_iscdi=true |