<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(10)</volume><submitter>Sung KC</submitter><pubmed_abstract>We aimed to test the association between low-density lipoprotein cholesterol (LDL-C) and cardiovascular disease (CVD), cancer, and all-cause mortality in non-statin users. A total of 347,971 subjects in Kangbuk Samsung Health Study (KSHS.57.4% men, mean follow up: 5.64 ± 3.27 years) were tested. To validate these associations, we analyzed data from another cohort (Korean genome and epidemiology study, KoGES, 182,943 subjects). All subjects treated with any lipid-lowering therapy and who died during the first 3 years of follow up were excluded. Five groups were defined according to baseline LDL-C concentration (&lt;70, 70-99, 100-129, 130-159, ≥160 mg/dL). A total of 2028 deaths occurred during follow-up in KSHS. The lowest LDL-C group (LDL &lt; 70 mg/dL) had a higher risk of all-cause mortality (HR 1.95, 1.55-2.47), CVD mortality (HR 2.02, 1.11-3.64), and cancer mortality (HR 2.06, 1.46-2.90) compared to the reference group (LDL 120-139 mg/dL). In the validation cohort, 2338 deaths occurred during follow-up. The lowest LDL-C group (LDL &lt; 70 mg/dL) had a higher risk of all-cause mortality (HR 1.81, 1.44-2.28) compared to the reference group. Low levels of LDL-C concentration are strongly and independently associated with increased risk of cancer, CVD, and all-cause mortality. These findings suggest that more attention is needed for subjects with no statin-induced decrease in LDL-C concentrations.</pubmed_abstract><journal>Journal of clinical medicine</journal><pagination>E1571</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6832139</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Low Levels of Low-Density Lipoprotein Cholesterol and Mortality Outcomes in Non-Statin Users.</pubmed_title><pmcid>PMC6832139</pmcid><pubmed_authors>Scorletti E</pubmed_authors><pubmed_authors>Sung KC</pubmed_authors><pubmed_authors>Kim JY</pubmed_authors><pubmed_authors>Ko SB</pubmed_authors><pubmed_authors>Byrne CD</pubmed_authors><pubmed_authors>Hyun DS</pubmed_authors><pubmed_authors>Ryu S</pubmed_authors><pubmed_authors>Lee JY</pubmed_authors><pubmed_authors>Huh JH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Low Levels of Low-Density Lipoprotein Cholesterol and Mortality Outcomes in Non-Statin Users.</name><description>We aimed to test the association between low-density lipoprotein cholesterol (LDL-C) and cardiovascular disease (CVD), cancer, and all-cause mortality in non-statin users. A total of 347,971 subjects in Kangbuk Samsung Health Study (KSHS.57.4% men, mean follow up: 5.64 ± 3.27 years) were tested. To validate these associations, we analyzed data from another cohort (Korean genome and epidemiology study, KoGES, 182,943 subjects). All subjects treated with any lipid-lowering therapy and who died during the first 3 years of follow up were excluded. Five groups were defined according to baseline LDL-C concentration (&lt;70, 70-99, 100-129, 130-159, ≥160 mg/dL). A total of 2028 deaths occurred during follow-up in KSHS. The lowest LDL-C group (LDL &lt; 70 mg/dL) had a higher risk of all-cause mortality (HR 1.95, 1.55-2.47), CVD mortality (HR 2.02, 1.11-3.64), and cancer mortality (HR 2.06, 1.46-2.90) compared to the reference group (LDL 120-139 mg/dL). In the validation cohort, 2338 deaths occurred during follow-up. The lowest LDL-C group (LDL &lt; 70 mg/dL) had a higher risk of all-cause mortality (HR 1.81, 1.44-2.28) compared to the reference group. Low levels of LDL-C concentration are strongly and independently associated with increased risk of cancer, CVD, and all-cause mortality. These findings suggest that more attention is needed for subjects with no statin-induced decrease in LDL-C concentrations.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Oct</publication><modification>2024-12-04T06:29:10.955Z</modification><creation>2020-05-21T19:05:08Z</creation></dates><accession>S-EPMC6832139</accession><cross_references><pubmed>31581520</pubmed><doi>10.3390/jcm8101571</doi></cross_references></HashMap>