{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,11]],"date-time":"2026-08-11T20:31:51Z","timestamp":1786480311487,"version":"build-2736575974"},"reference-count":58,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"9","funder":[{"DOI":"10.13039\/501100000274","name":"British Heart Foundation","doi-asserted-by":"publisher","award":["PG\/11\/66\/28982"],"award-info":[{"award-number":["PG\/11\/66\/28982"]}],"id":[{"id":"10.13039\/501100000274","id-type":"DOI","asserted-by":"publisher"}]},{"name":"Medical Research Foundation of Oregon"},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["K23 DK115683"],"award-info":[{"award-number":["K23 DK115683"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":["Kidney360"],"published-print":{"date-parts":[[2022,9,29]]},"abstract":"<jats:sec>\n                    <jats:title>Key Points<\/jats:title>\n                    <jats:p>\n                      <jats:list list-type=\"bullet\">\n                        <jats:list-item>\n                          <jats:p>\n                            The highest fibroblast growth factor 23 (FGF23) quartile had impaired VO\n                            <jats:sub>2<\/jats:sub>\n                            Max and ventilatory exercise response patterns compared with the lowest FGF23 quartile.\n                          <\/jats:p>\n                        <\/jats:list-item>\n                        <jats:list-item>\n                          <jats:p>\n                            FGF23 was associated with changes in VO\n                            <jats:sub>2<\/jats:sub>\n                            Max in advanced CKD and after restitution of the failing kidney by transplantation.\n                          <\/jats:p>\n                        <\/jats:list-item>\n                        <jats:list-item>\n                          <jats:p>FGF23 was only associated with the progression of left ventricular mass index in patients with advanced CKD, however this association was lost after adjustment for dialysis status in the final model and was not associated after kidney transplantation in all models.<\/jats:p>\n                        <\/jats:list-item>\n                      <\/jats:list>\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      Fibroblast growth factor 23 (FGF23) is a bone-derived phosphatonin that is elevated in chronic kidney disease (CKD) and has been implicated in the development of cardiovascular disease. It is unknown whether elevated FGF23 in CKD is associated with impaired cardiovascular functional capacity, as assessed by maximum exercise oxygen consumption (VO\n                      <jats:sub>2<\/jats:sub>\n                      Max). We sought to determine whether FGF23 is associated with cardiovascular functional capacity in patients with advanced CKD and after improvement of VO\n                      <jats:sub>2<\/jats:sub>\n                      Max by kidney transplantation.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>We performed secondary analysis of 235 patients from the Cardiopulmonary Exercise Testing in Renal Failure and After Kidney Transplantation (CAPER) cohort, which recruited patients with stage 5 CKD who underwent kidney transplantation or were waitlisted and hypertensive controls. All patients underwent cardiopulmonary exercise testing (CPET) and echocardiography and were followed longitudinally for 1 year after study enrollment.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Patients across FGF23 quartiles differed in BMI (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.004) and mean arterial pressure (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.001) but did not significantly differ in sex (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.5) or age (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.08) compared with patients with lower levels of FGF23. Patients with higher FGF23 levels had impaired VO\n                      <jats:sub>2<\/jats:sub>\n                      Max (Q1: 24.2\u00b14.8 ml\/min per kilogram; Q4: 18.6\u00b15.2 ml\/min per kilogram;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.001), greater left ventricular mass index (LVMI;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.001), reduced HR at peak exercise (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.001), and maximal workload (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.001). Kidney transplantation conferred a significant decline in FGF23 at 2 months (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.001) before improvement in VO\n                      <jats:sub>2<\/jats:sub>\n                      Max at 1 year (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.008). Multivariable regression modeling revealed that changes in FGF23 was significantly associated with VO\n                      <jats:sub>2<\/jats:sub>\n                      Max in advanced CKD (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.001) and after improvement after kidney transplantation (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.006). FGF23 was associated with LVMI before kidney transplantation (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.003), however this association was lost after adjustment for dialysis status (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.4). FGF23 was not associated with LVMI after kidney transplantation in all models.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>FGF23 levels are associated with alterations in cardiovascular functional capacity in advanced CKD and after kidney transplantation. FGF23 is only associated with structural cardiac adaptations in advanced CKD but this was modified by dialysis status, and was not associated after kidney transplantation.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.34067\/kid.0002192022","type":"journal-article","created":{"date-parts":[[2022,7,5]],"date-time":"2022-07-05T16:00:11Z","timestamp":1657036811000},"page":"1529-1541","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":7,"title":["FGF23 and Cardiovascular Structure and Function in Advanced Chronic Kidney Disease"],"prefix":"10.34067","volume":"3","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-4496-9967","authenticated-orcid":false,"given":"Arvin","family":"Halim","sequence":"first","affiliation":[{"name":"Division of Nephrology and Hypertension, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Heather N.","family":"Burney","sequence":"additional","affiliation":[{"name":"Department of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, Indiana"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1547-3041","authenticated-orcid":false,"given":"Xiaochun","family":"Li","sequence":"additional","affiliation":[{"name":"Department of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, Indiana"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7024-7103","authenticated-orcid":false,"given":"Yang","family":"Li","sequence":"additional","affiliation":[{"name":"Department of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, Indiana"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Claudia","family":"Tomkins","sequence":"additional","affiliation":[{"name":"Biochemistry Department, Kettering General Hospital NHS Foundation Trust, Kettering, United Kingdom"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrew M.","family":"Siedlecki","sequence":"additional","affiliation":[{"name":"Division of Renal Medicine, Brigham and Women\u2019s Hospital, Harvard Medical School, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3115-5000","authenticated-orcid":false,"given":"Tzong-shi","family":"Lu","sequence":"additional","affiliation":[{"name":"Division of Renal Medicine, Brigham and Women\u2019s Hospital, Harvard Medical School, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sahir","family":"Kalim","sequence":"additional","affiliation":[{"name":"Nephrology Division, Massachusetts General Hospital, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ravi","family":"Thadhani","sequence":"additional","affiliation":[{"name":"Mass General Brigham, Harvard Medical School, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sharon","family":"Moe","sequence":"additional","affiliation":[{"name":"Division of Nephrology and Hypertension, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Stephen M.S.","family":"Ting","sequence":"additional","affiliation":[{"name":"Department of Medicine, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Daniel","family":"Zehnder","sequence":"additional","affiliation":[{"name":"Department of Nephrology and Department of Acute Medicine, North Cumbria University Hospital NHS Trust, Carlisle, United Kingdom"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thomas F.","family":"Hiemstra","sequence":"additional","affiliation":[{"name":"School of Clinical Medicine, University of Cambridge; Clinical Trials Unit (CTU), Addenbrooke\u2019s Hospital, Cambridge, United Kingdom"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kenneth","family":"Lim","sequence":"additional","affiliation":[{"name":"Division of Nephrology and Hypertension, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2022,9,29]]},"reference":[{"key":"B1-20250825","doi-asserted-by":"crossref","first-page":"770","DOI":"10.1038\/nature05315","article-title":"Klotho converts canonical FGF receptor into a specific receptor for 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