Evidence map›Paper›PMID 31473619›Full record

ArticleBMJ open2019

C reactive protein level as a marker for dyslipidaemia, diabetes and metabolic syndrome: results from the Korea National Health and Nutrition Examination Survey.

Hyemin Jeong, Sun-Young Baek, Seon Woo Kim, Eun-Jung Park, Jaejoon Lee, Hyungjin Kim, Chan Hong Jeon

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 3 pooled it
4.0field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 3 syntheses or guidelines pooled it, 60 citations in OpenAlex.

  1. Pooled it
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  3. Can biomarkers be used to improve diagnosis and prediction of metabolic syndrome in childhood cancer survivors? A systematic review.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2021
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  15. Toxicity Profile ofBiochemistry research international · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Hyemin JeongDivision of Rheumatology, Department of Internal Medicine, Soonchunhyang University Hospital Bucheon, Bucheon, South Korea.
Sun-Young BaekStatistics and Data Center, Samsung Medical Center, Seoul, South Korea.
Seon Woo KimStatistics and Data Center, Samsung Medical Center, Seoul, South Korea.
Eun-Jung ParkDivision of Rheumatology, Department of Internal Medicine, National Medical Center, Seoul, South Korea.
Jaejoon LeeDepartment of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Hyungjin Kim *Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea chjeon@gmail.com passiondoc@gmail.com.
Chan Hong Jeon *Division of Rheumatology, Department of Internal Medicine, Soonchunhyang University Hospital Bucheon, Bucheon, South Korea chjeon@gmail.com passiondoc@gmail.com.ORCID 0000-0002-2430-7264
Samsung Medical Center · KRSoonchunhyang University Hospital Seoul · KRNational Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePlasma C reactive protein (CRP) is a marker of inflammation, and increased plasma CRP is reported in many diseases, including cardiovascular disease, diabetes, metabolic syndrome, arthritis and malignancies. The aim of the study was to evaluate the association between plasma CRP levels and cardiovascular disease, metabolic syndrome, malignancies and other comorbidities.

designA retrospective, cross-sectional survey study.

settingLarge population survey in Korea.

methodsA total of 5887 (weighted n=40 251 868) participants aged 19 years or older from the 2016 Korea National Health and Nutrition Examination Survey were included for analysis. Weighted prevalence and OR of comorbidities were analysed according to the continuous variable of log plasma high-sensitivity CRP levels.

resultsThe mean age was 46.7±0.37 years and the median plasma CRP was 0.58 mg/L (IQR 0.36-1.09). The mean plasma CRP levels were higher in participants with cardiovascular diseases and cardiovascular risk factors, osteoarthritis, rheumatoid arthritis, pulmonary tuberculosis, and several cancers, including gastric, colon, breast and cervix, than in the general population. In the multivariable analysis, plasma CRP concentration was associated with increased prevalence of hypertriglyceridaemia (OR 1.157, 95% CI 1.040 to 1.287, p=0.007), diabetes (OR 1.204, 95% CI 1.058 to 1.371, p=0.005) and metabolic syndrome (OR 1.228, 95% CI 1.112 to 1.357, p<0.001) after adjustment for socioeconomic and lifestyle characteristics. There was no significant association between plasma CRP level and cancers.

conclusionPlasma CRP was associated with an increased risk of dyslipidaemia, diabetes and metabolic syndrome in the general population.

Indexed as

BiomarkersC-Reactive ProteinCross-Sectional StudiesDiabetes MellitusDyslipidemiasFemaleHumansLife StyleLogistic ModelsMaleMetabolic SyndromeMiddle AgedMultivariate AnalysisNutrition SurveysPrevalenceRepublic of KoreaBiomarkersC-Reactive Proteinc reactive proteindiabetesdyslipidaemiametabolic syndrome

Identifiers

PMID31473619
PMCPMC6720331
OpenAlexW2971011519

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.