<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Freedman BI</submitter><funding>NIDDK NIH HHS</funding><funding>NIMHD NIH HHS</funding><funding>AstraZeneca</funding><pagination>1765-1778</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8425659</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>32(7)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>&lt;i>APOL1&lt;/i> variants contribute to the markedly higher incidence of ESKD in Blacks compared with Whites. Genetic testing for these variants in patients with African ancestry who have nephropathy is uncommon, and no specific treatment or management protocol for &lt;i>APOL1&lt;/i>-associated nephropathy currently exists.&lt;h4>Methods&lt;/h4>A multidisciplinary, racially diverse group of 14 experts and patient advocates participated in a Delphi consensus process to establish practical guidance for clinicians caring for patients who may have &lt;i>APOL1&lt;/i>-associated nephropathy. Consensus group members took part in three anonymous voting rounds to develop consensus statements relating to the following: (&lt;i>1&lt;/i>) counseling, genotyping, and diagnosis; (&lt;i>2&lt;/i>) disease awareness and e</pubmed_abstract><journal>Journal of the American Society of Nephrology : JASN</journal><pubmed_title>Diagnosis, Education, and Care of Patients with &lt;i>APOL1&lt;/i>-Associated Nephropathy: A Delphi Consensus and Systematic Review.</pubmed_title><pmcid>PMC8425659</pmcid><funding_grant_id>DP2 DK124891</funding_grant_id><funding_grant_id>R01 MD016401</funding_grant_id><pubmed_authors>Divers J</pubmed_authors><pubmed_authors>Roberts GV</pubmed_authors><pubmed_authors>Freedman BI</pubmed_authors><pubmed_authors>Burke W</pubmed_authors><pubmed_authors>Norris KC</pubmed_authors><pubmed_authors>Gadegbeku CA</pubmed_authors><pubmed_authors>Kopp JB</pubmed_authors><pubmed_authors>Knight R</pubmed_authors><pubmed_authors>Blacksher E</pubmed_authors><pubmed_authors>Hall ME</pubmed_authors><pubmed_authors>Jones-Smith T</pubmed_authors><pubmed_authors>Gbadegesin R</pubmed_authors><pubmed_authors>Eberhard L</pubmed_authors><pubmed_authors>Kovesdy CP</pubmed_authors><pubmed_authors>Olabisi OA</pubmed_authors><pubmed_authors>Sedor JR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Diagnosis, Education, and Care of Patients with &lt;i>APOL1&lt;/i>-Associated Nephropathy: A Delphi Consensus and Systematic Review.</name><description>&lt;h4>Background&lt;/h4>&lt;i>APOL1&lt;/i> variants contribute to the markedly higher incidence of ESKD in Blacks compared with Whites. Genetic testing for these variants in patients with African ancestry who have nephropathy is uncommon, and no specific treatment or management protocol for &lt;i>APOL1&lt;/i>-associated nephropathy currently exists.&lt;h4>Methods&lt;/h4>A multidisciplinary, racially diverse group of 14 experts and patient advocates participated in a Delphi consensus process to establish practical guidance for clinicians caring for patients who may have &lt;i>APOL1&lt;/i>-associated nephropathy. Consensus group members took part in three anonymous voting rounds to develop consensus statements relating to the following: (&lt;i>1&lt;/i>) counseling, genotyping, and diagnosis; (&lt;i>2&lt;/i>) disease awareness and e</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jul</publication><modification>2026-05-08T01:08:39.014Z</modification><creation>2022-07-11T07:06:53.308Z</creation></dates><accession>S-EPMC8425659</accession><cross_references><pubmed>33853887</pubmed><doi>10.1681/ASN.2020101399</doi><doi>10.1681/asn.2020101399</doi></cross_references></HashMap>