<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>25(1)</volume><submitter>Fan Z</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Hyperphosphatemia is common in chronic kidney disease (CKD), associated with higher mortality in dialysis patients. Its impact in non-dialysis patients, especially those with preserved kidney function, remains uncertain.&lt;h4>Methods&lt;/h4>A prospective cohort study was conducted using data from the National Health and Nutrition Examination Survey (2001-2008). Serum phosphorus was analyzed as a continuous variable, or categorized into three groups: &lt; 3.5 mg/dL, 3.5 to &lt; 4.5 mg/dL, and ≥ 4.5 mg/dL. Cox proportional hazards models were used to analyze the association between phosphorus with all-cause and cardiovascular disease (CVD) mortality, with or without adjustment for age, sex, race, hemoglobin, estimated glomerular filtration rate (eGFR), serum albumin, serum calcium, 25(OH)D, obesity, hypertension, diabetes, and CVD.&lt;h4>Results&lt;/h4>A total of 7694 participants were included in the analysis, representing 28 million CKD patients in the United States. During mean 92 months of follow up, 2708 all-cause deaths (including 969 CVD deaths) were observed. Per 1 mg/dL increase in phosphorus was associated with a 13% and 24% increased risk of all-cause mortality (hazard ratio [HR], 1.13; 95%CI, 1.02-1.24) and CVD mortality (HR, 1.24; 95%CI, 1.07-1.45), respectively. Compared with the &lt; 3.5 mg/dL, phosphorus ≥ 4.5 mg/dL was associated with a 28% and 57% increased risk of all-cause mortality (HR, 1.28; 95%CI, 1.05-1.55) and CVD mortality (HR, 1.57; 95CI, 1.19-2.08), respectively. In participants with eGFR &lt; 60 ml/min/1.73m&lt;sup>2&lt;/sup>, elevated phosphorus (≥ 4.5 mg/ dL) were significantly associated with increased risk of all-cause mortality (HR, 1.36; 95%CI, 1.07-1.72). No significant association was observed in eGFR ≥ 60 ml/min/1.73m&lt;sup>2&lt;/sup> group (HR, 1.31; 95%CI, 0.86-1.99). This correlation does not differ significantly between subgroups defined by eGFR level (P for interaction = 0.889).&lt;h4>Conclusion&lt;/h4>Serum phosphorus above 4.5 mg/dL is significantly associated with a 28% and 57% increased risk of all-cause and CVD death in non-dialysis CKD patients, respectively. This relationship still demonstrated in patients with eGFR &lt; 60 ml/min/1.73m&lt;sup>2&lt;/sup>. However, for population with eGFR ≥ 60 ml/min/1.73m&lt;sup>2&lt;/sup>, further verification is needed.</pubmed_abstract><journal>BMC nephrology</journal><pagination>89</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10918918</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Relationship between serum phosphorus and mortality in non-dialysis chronic kidney disease patients: evidence from NHANES 2001-2018.</pubmed_title><pmcid>PMC10918918</pmcid><pubmed_authors>Jiang Y</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Fan Z</pubmed_authors><pubmed_authors>Li R</pubmed_authors><pubmed_authors>Pan M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Relationship between serum phosphorus and mortality in non-dialysis chronic kidney disease patients: evidence from NHANES 2001-2018.</name><description>&lt;h4>Background&lt;/h4>Hyperphosphatemia is common in chronic kidney disease (CKD), associated with higher mortality in dialysis patients. Its impact in non-dialysis patients, especially those with preserved kidney function, remains uncertain.&lt;h4>Methods&lt;/h4>A prospective cohort study was conducted using data from the National Health and Nutrition Examination Survey (2001-2008). Serum phosphorus was analyzed as a continuous variable, or categorized into three groups: &lt; 3.5 mg/dL, 3.5 to &lt; 4.5 mg/dL, and ≥ 4.5 mg/dL. Cox proportional hazards models were used to analyze the association between phosphorus with all-cause and cardiovascular disease (CVD) mortality, with or without adjustment for age, sex, race, hemoglobin, estimated glomerular filtration rate (eGFR), serum albumin, serum calcium, 25(OH)D, obesity, hypertension, diabetes, and CVD.&lt;h4>Results&lt;/h4>A total of 7694 participants were included in the analysis, representing 28 million CKD patients in the United States. During mean 92 months of follow up, 2708 all-cause deaths (including 969 CVD deaths) were observed. Per 1 mg/dL increase in phosphorus was associated with a 13% and 24% increased risk of all-cause mortality (hazard ratio [HR], 1.13; 95%CI, 1.02-1.24) and CVD mortality (HR, 1.24; 95%CI, 1.07-1.45), respectively. Compared with the &lt; 3.5 mg/dL, phosphorus ≥ 4.5 mg/dL was associated with a 28% and 57% increased risk of all-cause mortality (HR, 1.28; 95%CI, 1.05-1.55) and CVD mortality (HR, 1.57; 95CI, 1.19-2.08), respectively. In participants with eGFR &lt; 60 ml/min/1.73m&lt;sup>2&lt;/sup>, elevated phosphorus (≥ 4.5 mg/ dL) were significantly associated with increased risk of all-cause mortality (HR, 1.36; 95%CI, 1.07-1.72). No significant association was observed in eGFR ≥ 60 ml/min/1.73m&lt;sup>2&lt;/sup> group (HR, 1.31; 95%CI, 0.86-1.99). This correlation does not differ significantly between subgroups defined by eGFR level (P for interaction = 0.889).&lt;h4>Conclusion&lt;/h4>Serum phosphorus above 4.5 mg/dL is significantly associated with a 28% and 57% increased risk of all-cause and CVD death in non-dialysis CKD patients, respectively. This relationship still demonstrated in patients with eGFR &lt; 60 ml/min/1.73m&lt;sup>2&lt;/sup>. However, for population with eGFR ≥ 60 ml/min/1.73m&lt;sup>2&lt;/sup>, further verification is needed.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-04T12:35:09.005Z</modification><creation>2025-04-04T12:35:09.005Z</creation></dates><accession>S-EPMC10918918</accession><cross_references><pubmed>38448815</pubmed><doi>10.1186/s12882-024-03525-x</doi></cross_references></HashMap>