Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Video

Updated: Jul 3, 2026

Supervised Machine Learning for Semi-Quantification of Extracellular DNA in Glomerulonephritis
09:16

Supervised Machine Learning for Semi-Quantification of Extracellular DNA in Glomerulonephritis

Published on: June 18, 2020

Exploring causality between peripheral blood B cell subtypes and membranous nephropathy: a two-sample Mendelian

Zhiyong Zhang1, Jun Zhao1, Ting Yan1

  • 1Department of Nephrology, The Sixth Medical Center of PLA General Hospital, Beijing, China.

Archives of Medical Science : AMS
|June 17, 2026
PubMed
Summary

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Comparison of brain gray matter volume changes in peritoneal dialysis and hemodialysis patients with chronic kidney disease: a VBM study.

Frontiers in neuroscience·2024
Same author

Azvudine therapy of common COVID-19 in hemodialysis patients.

Journal of medical virology·2023
Same author

Toll-Like Receptors Signaling Pathway of Quercetin Regulating Avian Beta-Defensin in the Ileum of Broilers.

Frontiers in cell and developmental biology·2022
Same author

The Effects and Mechanism of Quercetin Dietary Supplementation in Streptozotocin-Induced Hyperglycemic Arbor Acre Broilers.

Oxidative medicine and cellular longevity·2020
Same author

Bacteriostatic Effect of Quercetin as an Antibiotic Alternative In Vivo and Its Antibacterial Mechanism In Vitro.

Journal of food protection·2017
Same author

Risk factors of prognosis after acute kidney injury in hospitalized patients.

Frontiers of medicine·2017

This study used Mendelian randomization to investigate how peripheral blood B cell subtypes influence membranous nephropathy (MN). Certain B cell subtypes and markers are genetically linked to a reduced risk of developing this autoimmune kidney disease.

Area of Science:

  • Immunology
  • Nephrology
  • Genetics

Background:

  • Membranous nephropathy (MN) is an autoimmune glomerular disease causing nephrotic syndrome.
  • Understanding the role of peripheral blood B cell subtypes in MN pathogenesis is crucial.

Purpose of the Study:

  • To explore the potential causal influence of peripheral blood B cell subtypes on the risk of developing membranous nephropathy (MN).
  • To utilize Mendelian randomization (MR) to investigate genetic associations between B cell subtypes and MN.

Main Methods:

  • Mendelian randomization (MR) analysis using genome-wide association study (GWAS) data for single-nucleotide polymorphisms (SNPs) related to peripheral blood B cells and MN.
  • Employed instrumental variable weighted (IVW), weighted median, weighted mode, and MR-Egger regression methods.
Keywords:
B cellMendelian randomizationgenome-wide association studymembranous nephropathy

Related Experiment Videos

Last Updated: Jul 3, 2026

Supervised Machine Learning for Semi-Quantification of Extracellular DNA in Glomerulonephritis
09:16

Supervised Machine Learning for Semi-Quantification of Extracellular DNA in Glomerulonephritis

Published on: June 18, 2020

  • Conducted sensitivity analyses including MR-Egger, MR-PRESSO, Cochran's Q test, and leave-one-out analysis to ensure result robustness.
  • Main Results:

    • Several peripheral blood B cell subtypes and their marker expressions were significantly associated with a decreased risk of MN.
    • Key findings include associations for IgD+ CD24-B cell absolute count, B-cell activating factor receptor (BAFF-R) on various B cell subsets (IgD+ CD24-, IgD+ CD38dim, IgD- CD27-), CD19 on IgD-CD24-B cells, CD24 on switched memory B cells, and CD25 on switched memory B cells.
    • Sensitivity analyses confirmed the stability and reliability of these genetic associations.

    Conclusions:

    • This MR study provides evidence for a potential genetic causal relationship between specific peripheral blood B cell subtypes and membranous nephropathy.
    • The findings enhance the understanding of the immunological underpinnings of MN.
    • These insights may contribute to the future development of personalized medicine approaches for MN.