ArticleBMC cardiovascular disorders2025
The association of gene polymorphisms in SREBP and its interaction with nutritional status on blood pressure phenotypes among children: a cross-sectional study.
Article in BMC cardiovascular disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- SREBP gene polymorphisms and ambulatory blood pressure parameters in Chinese adolescents: a cross-sectional study.European journal of pediatrics · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
Abstract
introductionPrevious studies have confirmed that the SREBP polymorphisms are associated with dyslipidemia. However, no researchers investigated the association between SREBP polymorphisms and blood pressure phenotypes in children.
methodsA convenient cluster sampling method was adopted to conduct field survey in three middle schools. A total of 872 children were included in this cross-sectional study final analysis. Matrix-supported laser release/ionization time-of-flight mass spectrometry was used for genotyping of SREBP polymorphism. The association between SREBP polymorphisms and blood pressure phenotypes was analyzed by multivariable linear regression and Logistic regression analysis. A Bonferroni-corrected threshold of P < 0.025 (SREBP1) or P < 0.0125 (SREBP2) was considered significant.
resultsAfter adjusting for age, sex, age squared and BMI, individuals with GA/AA genotype of SREBP1/rs11868035 had higher systolic blood pressure (SBP) (β = 7.34, P = 0.004) than GG genotype, and SREBP1/rs2297508 C allele carriers were positively associated with SBP (β = 7.19, P = 0.008). A significant interaction between SREBP2/rs2228314 and gender on the risk of High Blood Pressure (HBP) (P
conclusionsSREBP polymorphisms were significantly associated with blood pressure in children. It provides possible clues for personalized prevention and intervention of HBP in children from the perspective of genetic susceptibility.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.