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Record W2181652150

The Relationship between Inflammation, Metabolic Syndrome and Markers of Cardiometabolic Disease among Canadian Adults

2011· article· en· W2181652150 on OpenAlexaboutno aff
Darren R. Brenner, Paul Arora, Bibiana García‐Bailo, Howard Morrison, Ahmed El‐Sohemy, Mohamed A. Karmali, Alaa Badawi, Dalla Lana

Bibliographic record

VenueJournal of Diabetes & Metabolism · 2011
Typearticle
Languageen
FieldMedicine
TopicAdipokines, Inflammation, and Metabolic Diseases
Canadian institutionsnot available
Fundersnot available
KeywordsMetabolic syndromeMedicineNational Cholesterol Education ProgramInternal medicineDiseaseHomocysteineDiabetes mellitusApolipoprotein BC-reactive proteinPopulationNational Health and Nutrition Examination SurveyEndocrinologyCholesterolInflammationEnvironmental health
DOInot available

Abstract

fetched live from OpenAlex

Background: The metabolic syndrome (MetS) is a well-established risk factor for cardiometabolic disease. However, the association between MetS, and its components, with the metabolic phenotypes and inflammatory markers that are risk factor for cardiometabolic disease has not been explored in the general population. The present study examines this association among Canadian adults and explores the changes in the profile of a number of metabolic and inflammatory markers associated with cardiometabolic disease at various MetS stages. Methods: Serum levels of apolipoprotein A1 and B (Apo-A1, -B), total:HDL-cholesterol (HDL-C) ratio, C-reactive protein (CRP), fibrinogen, glycosylated haemoglobin (HbA1c) and homocysteine were determined in 1,818 non-diabetic adults (16-79 years of age) from the Canadian Health Measures Survey (CHMS). The definition of MetS components was based on the National Cholesterol Education Program, Adult Treatment Panel III criteria. Taylor-series expansion methods for complex survey data were used to estimate variances. Generalized linear models adjusted for age, sex, physical activity, smoking status, use of medications and ethnicity were used to quantify the relationship between the metabolic phenotypes and inflammatory markers associated with risk to cardiometabolic disease and the number of MetS components. Results: The prevalence of the MetS (i.e., with three or more MetS components) among the study subjects was 8.9%, with 31.8% having at least one component. As expected, metabolic markers such as total: HDL-C, Apo-B and HbA1c were all significantly increased as the number of MetS components increased whereas Apo-A was decreased. We also observed a significant association between the number of MetS components and the serum levels of inflammatory biomarkers such as CRP and fibrinogen, but not homocysteine. Mean serum levels of these markers were significantly elevated as the numbers of MetS components increased. Strong correlations were noted between CRP, fibrinogen, and homocysteine and the individual components of the MetS. Conclusions: There is an apparent profile of metabolic phenotypes and inflammatory biomarkers, known to be related to the cardiometabolic disease risk, that emerges as MetS manifests with increasing the number of its components. These findings may permit proposing a metabolic trait that predisposes to MetS and may permit developing an effective approach for early risk prediction and intervention.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.015
Threshold uncertainty score0.088

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.003
Science and technology studies0.0020.000
Scholarly communication0.0010.000
Open science0.0010.001
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0020.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.017
GPT teacher head0.231
Teacher spread0.214 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations2
Published2011
Admission routes1
Has abstractyes

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