Home Research Feeds Alteration of gut microbiota associated with hypertension in children

Alteration of gut microbiota associated with hypertension in childrenOriginal paper

Researched by:

  • Karen Pendergrass

Last Updated: 2026-07-05

Karen Pendergrass
Karen Pendergrass

Karen Pendergrass is a microbiome researcher specializing in microbiome-targeted interventions (MBTIs). She systematically analyzes scientific literature to identify microbial patterns, develop hypotheses, and validate interventions. As the founder of the Microbiome Signatures Database, she bridges microbiome research with clinical practice. In 2012, based on her own investigative research, she became the first documented case of FMT for Celiac Disease, four years before the first published case study.

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Location
China
Sample Site
Feces
Species
Homo sapiens

What was studied?

This case-control study asked whether gut microbiota differ between children with confirmed hypertension and children with normal blood pressure. Researchers analysed stool samples using 16S ribosomal RNA gene sequencing of the V3-V4 region. Hypertension was defined rigorously, using elevated blood pressure measured on three separate visits at least two weeks apart. The team compared diversity, composition, and genus abundance between groups. They then tested whether gut bacteria could improve identification of hypertension beyond body mass index.

Who was studied?

The sample was 102 Chinese children aged 10 to 14 years from the Huantai Childhood Cardiovascular Health Cohort in Shandong, China. Half (51) had hypertension confirmed on three occasions, and 51 had normal blood pressure. Boys made up 64.7% of each group. Children with hypertension had higher body mass index, waist circumference, and triglycerides. None had used antibiotics or had gastrointestinal illness in the prior three months. Fecal samples were collected alongside anthropometric and blood measurements.

What were the most important findings?

Children with hypertension had lower gut microbial diversity and richness than children with normal blood pressure (Shannon P=0.005, Chao P=0.006, Ace P=0.022). Community structure also differed by principal coordinate analysis. Several genera decreased in the hypertension group: Blautia (P=0.042), Coprococcus (P=0.042), Eubacterium ventriosum group (P=0.027), Christensenellaceae R-7 group (P=0.027), and a norank Lachnospiraceae taxon (P=0.015). Adding the norank Lachnospiraceae taxon and Dorea to body mass index raised the discrimination for hypertension to an area under the curve of 0.95 (95% CI 0.91 to 0.99), improving classification by 12% (IDI=0.12).

What are the greatest implications of this study?

The results suggest gut microbiota disturbances are associated with childhood hypertension and may aid early identification. Several depleted genera are fiber-fermenting, short-chain fatty acid producers with plausible protective roles. Associations varied by sex and age, with lower diversity mainly in boys and pubertal children. The design is cross-sectional, so it cannot establish that microbiota changes precede hypertension. Findings come from one Chinese city and need confirmation in prospective, diverse cohorts before clinical use.

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