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C-reactive protein to albumin ratio and risk of incident metabolic syndrome in community-dwelling adults: longitudinal findings over a 12-year follow-up period
DC Field | Value | Language |
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dc.contributor.author | 이용제 | - |
dc.date.accessioned | 2024-12-06T02:47:59Z | - |
dc.date.available | 2024-12-06T02:47:59Z | - |
dc.date.issued | 2024-10 | - |
dc.identifier.issn | 1355-008X | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/200902 | - |
dc.description.abstract | Aim : The C-reactive protein to albumin (CRP/Alb) ratio has emerged as a novel biomarker for various inflammatory diseases. This study aimed to evaluate the association between the CRP/Alb ratio and incident metabolic syndrome (MetS) with a large-sample, community-based Korean cohort over a 12-year follow-up period. Materials and methods : Among 10,030 participants, a total of 6205 participants aged 40.69 years without MetS were selected from the Korean Genome and Epidemiology Study (KoGES). The baseline CRP/Alb ratio was divided into quartiles. The definition of newly developed MetS was the one proposed by the 2009 Joint Interim Statement of Circulation. Hazard ratios (HRs) with 95% confidence intervals (CIs) for incident MetS were calculated using multivariable Cox proportional hazards regression models after adjusting for potentially confounding variables. Results : During the 12-year follow-up period, MetS developed in 2535 subjects (40.9%, 2535/6205) with an incidence rate of 5.6.11.9 (over 2 years). Compared to the reference first quartiles, the HRs (95% CIs) of incident MetS in the second, third, and fourth quartiles increased in a dose-response manner. Compared to the reference quartile, the HRs (95% CIs) of the incidence of MetS for the second, third, and fourth quartiles of CRP/Alb ratio were 1.12 (0.99.1.27), 1.24 (1.11.1.40), and 1.51 (1.34.1.69) after adjusting for age, sex, smoking status, alcohol intake, physical activity, total cholesterol, mean arterial pressure, HOMA-IR, and total energy intake. Conclusions : High CRP/Alb ratio at baseline may be a useful surrogate indicator of future incident MetS. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Humana Press | - |
dc.relation.isPartOf | ENDOCRINE | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Biomarkers* / blood | - |
dc.subject.MESH | C-Reactive Protein* / analysis | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Follow-Up Studies | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Incidence | - |
dc.subject.MESH | Independent Living / statistics & numerical data | - |
dc.subject.MESH | Longitudinal Studies | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Metabolic Syndrome* / blood | - |
dc.subject.MESH | Metabolic Syndrome* / epidemiology | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Republic of Korea / epidemiology | - |
dc.subject.MESH | Risk Factors | - |
dc.subject.MESH | Serum Albumin / analysis | - |
dc.title | C-reactive protein to albumin ratio and risk of incident metabolic syndrome in community-dwelling adults: longitudinal findings over a 12-year follow-up period | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Family Medicine (가정의학교실) | - |
dc.contributor.googleauthor | Taekyeong Lim | - |
dc.contributor.googleauthor | Yong-Jae Lee | - |
dc.identifier.doi | 10.1007/s12020-024-03875-4 | - |
dc.contributor.localId | A02982 | - |
dc.relation.journalcode | J00768 | - |
dc.identifier.eissn | 1559-0100 | - |
dc.identifier.pmid | 38771483 | - |
dc.identifier.url | https://link.springer.com/article/10.1007/s12020-024-03875-4 | - |
dc.subject.keyword | C-reactive protein to albumin ratio | - |
dc.subject.keyword | Inflammation | - |
dc.subject.keyword | Insulin resistance | - |
dc.subject.keyword | Metabolic syndrome | - |
dc.contributor.alternativeName | Lee, Yong Jae | - |
dc.contributor.affiliatedAuthor | 이용제 | - |
dc.citation.volume | 86 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 156 | - |
dc.citation.endPage | 162 | - |
dc.identifier.bibliographicCitation | ENDOCRINE, Vol.86(1) : 156-162, 2024-10 | - |
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