<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Faye M</submitter><funding>GlaxoSmithKline</funding><funding>Agence Nationale de la Recherche</funding><funding>Recherche Clinique</funding><funding>MSD France</funding><funding>Fresenius Medical Care</funding><funding>The Inserm</funding><funding>Merck Sharp &amp;amp; Dohme</funding><funding>Programme hospitalier de recherche clinique</funding><funding>Sanofi</funding><pagination>1588-1597</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9718050</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(11)</volume><pubmed_abstract>&lt;h4>Background and objectives&lt;/h4>Late stages of CKD are characterized by significant symptom burden. This study aimed to identify subgroups within the 5-year trajectories of symptom evolution in patients with CKD and to describe associated patient characteristics and outcomes.&lt;h4>Design, setting, participants, &amp; measurements&lt;/h4>Among 2787 participants (66% men) with eGFR &lt;60 ml/min per 1.73 m&lt;sup>2&lt;/sup> enrolled in the CKD-Renal Epidemiology and Information Network (CKD-REIN) cohort study from July 2013 to May 2016, we assessed symptoms annually using the Kidney Disease Quality of Life-36 (KDQOL-36) questionnaire until December 2020. A total of 9121 measures were reported over follow-up; all participants had symptoms scored for at least one time point. We used a joint latent class-mixed model to distinguish profiles of symptom trajectories.&lt;h4>Results&lt;/h4>Patient mean age (±SD) at baseline was 67±13 years, and mean eGFR was 33±13 ml/min per 1.73 m&lt;sup>2&lt;/sup>. The prevalence of each symptom ranged from 24% (chest pain) to 83% (fatigue), and 98% of participants reported at least one symptom. After a median (interquartile range) follow-up of 5.3 (3.4-6.0) years, 690 participants initiated KRT, and 490 died before KRT. We identified two profiles of symptom trajectories: a "worse symptom score and worsening trajectory" in 31% of participants, characterized by a low initial symptom score that worsened more than ten points over time, and a "better symptom score and stable trajectory" in 69% of participants, characterized by a high initial score that remained stable. Participants in the worse symptom score and worsening trajectory group had more risk factors for CKD progression at baseline, worse quality of life, and a higher risk of KRT and death before KRT than other participants.&lt;h4>Conclusions&lt;/h4>This study highlights a significant worsening of symptoms in about one third of the participants, whereas the majority reported low symptom severity throughout the study.</pubmed_abstract><journal>Clinical journal of the American Society of Nephrology : CJASN</journal><pubmed_title>Five-Year Symptom Trajectories in Nondialysis-Dependent CKD Patients.</pubmed_title><pmcid>PMC9718050</pmcid><funding_grant_id>ANR-IA-COH-2012/3731</funding_grant_id><pubmed_authors>Legrand K</pubmed_authors><pubmed_authors>Liabeuf S</pubmed_authors><pubmed_authors>Massy ZA</pubmed_authors><pubmed_authors>CKD-REIN Study Group</pubmed_authors><pubmed_authors>Fouque D</pubmed_authors><pubmed_authors>Le Gall L</pubmed_authors><pubmed_authors>Speyer E</pubmed_authors><pubmed_authors>Leffondre K</pubmed_authors><pubmed_authors>Ayav C</pubmed_authors><pubmed_authors>Alencar de Pinho N</pubmed_authors><pubmed_authors>Faye M</pubmed_authors><pubmed_authors>Pecoits Filho R</pubmed_authors><pubmed_authors>Laville M</pubmed_authors><pubmed_authors>Jacquelinet C</pubmed_authors><pubmed_authors>Stengel B</pubmed_authors><pubmed_authors>Frimat L</pubmed_authors><pubmed_authors>Omorou AY</pubmed_authors><pubmed_authors>Combe C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Five-Year Symptom Trajectories in Nondialysis-Dependent CKD Patients.</name><description>&lt;h4>Background and objectives&lt;/h4>Late stages of CKD are characterized by significant symptom burden. This study aimed to identify subgroups within the 5-year trajectories of symptom evolution in patients with CKD and to describe associated patient characteristics and outcomes.&lt;h4>Design, setting, participants, &amp; measurements&lt;/h4>Among 2787 participants (66% men) with eGFR &lt;60 ml/min per 1.73 m&lt;sup>2&lt;/sup> enrolled in the CKD-Renal Epidemiology and Information Network (CKD-REIN) cohort study from July 2013 to May 2016, we assessed symptoms annually using the Kidney Disease Quality of Life-36 (KDQOL-36) questionnaire until December 2020. A total of 9121 measures were reported over follow-up; all participants had symptoms scored for at least one time point. We used a joint latent class-mixed model to distinguish profiles of symptom trajectories.&lt;h4>Results&lt;/h4>Patient mean age (±SD) at baseline was 67±13 years, and mean eGFR was 33±13 ml/min per 1.73 m&lt;sup>2&lt;/sup>. The prevalence of each symptom ranged from 24% (chest pain) to 83% (fatigue), and 98% of participants reported at least one symptom. After a median (interquartile range) follow-up of 5.3 (3.4-6.0) years, 690 participants initiated KRT, and 490 died before KRT. We identified two profiles of symptom trajectories: a "worse symptom score and worsening trajectory" in 31% of participants, characterized by a low initial symptom score that worsened more than ten points over time, and a "better symptom score and stable trajectory" in 69% of participants, characterized by a high initial score that remained stable. Participants in the worse symptom score and worsening trajectory group had more risk factors for CKD progression at baseline, worse quality of life, and a higher risk of KRT and death before KRT than other participants.&lt;h4>Conclusions&lt;/h4>This study highlights a significant worsening of symptoms in about one third of the participants, whereas the majority reported low symptom severity throughout the study.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2026-05-28T22:36:21.191Z</modification><creation>2026-04-08T03:23:59.71Z</creation></dates><accession>S-EPMC9718050</accession><cross_references><pubmed>36307136</pubmed><doi>10.2215/CJN.06140522</doi><doi>10.2215/cjn.06140522</doi></cross_references></HashMap>