Evidence map›Paper›PMID 24763111›Full record

ArticleNutrients2014

High plasma homocysteine increases risk of metabolic syndrome in 6 to 8 year old children in rural Nepal.

Mohsin Yakub, Kerry J Schulze, Subarna K Khatry, Christine P Stewart, Parul Christian, Keith P West

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Hyperhomocysteinemia as a Metabolic Risk Factor for Glucose Intolerance Among High-Risk Groups of Chinese Adults.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  9. Prevalence of Homocysteine-Related Hypertension in Patients With Chronic Kidney Disease.Journal of clinical hypertension (Greenwich, Conn.) · 2017
    Article
  10. Article
  11. Article
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

6 authors at 2 institutions in 1 country.

Mohsin YakubDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA. myakub1@jhu.edu.
Kerry J SchulzeDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA. kschulz1@jhu.edu.
Subarna K KhatryNepal Nutrition Intervention Project-Sarlahi, Tripureswor, Kathmandu 45104, Nepal. skk@mos.com.np.
Christine P StewartProgram in International and Community Nutrition, University of California, Davis, CA 95616, USA. cpstewart@ucdavis.edu.
Parul ChristianDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA. pchristi@jhsph.edu.
Keith P WestDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA. kwest@jhsph.edu.
Johns Hopkins University · USUniversity of California, Davis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Little attention has been given to the association of plasma homocysteine (Hcy) and metabolic syndrome (MetS) in children. We have evaluated the risk of MetS with plasma Hcy in a cohort of 6 to 8 year old rural Nepalese children, born to mothers who had participated in an antenatal micronutrient supplementation trial. We assessed Hcy in plasma from a random selection of n = 1000 children and determined the relationship of elevated Hcy (>12.0 μmol/L) to MetS (defined as the presence of any three of the following: abdominal adiposity (waist circumference ≥ 85th percentile of the study population), high plasma glucose (≥ 85th percentile), high systolic or diastolic blood pressure (≥ 90th percentile of reference population), triglyceride ≥ 1.7 mmol/L and high density lipoprotein < 0.9 mmol/L.) and its components. There was an increased risk of low high-density lipoproteins (HDL), [odds ratios (OR) = 1.77, 95% confidence intervals (CI) = 1.08-2.88; p = 0.020], high blood pressure [OR = 1.60, 95% CI = 1.10-2.46; p = 0.015] and high body mass index (BMI) [OR = 1.98, 95% CI = 1.33-2.96; p = 0.001] with elevated Hcy. We observed an increased risk of MetS (OR = 1.75, 95% CI = 1.06-2.90; p = 0.029) with elevated Hcy in age and gender-adjusted logistic regression models. High plasma Hcy is associated with increased risk of MetS and may have implications for chronic disease later in life.

Indexed as

Rural PopulationBiomarkersBlood PressureBody Mass IndexChildCholesterol, HDLCholesterol, LDLCross-Sectional StudiesFemaleFollow-Up StudiesHomocysteineHumansHyperhomocysteinemiaLogistic ModelsMaleMetabolic SyndromeBiomarkersCholesterol, HDLCholesterol, LDLHomocysteineTriglycerides

Identifiers

PMID24763111
PMCPMC4011057
OpenAlexW2094441861

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.