# Discovering the Consequences of Genetic Variation in Nephrin on Kidney Diseases and Traits in Biobank Populations

> **NIH NIH F32** · BOSTON CHILDREN'S HOSPITAL · 2024 · $87,064

## Abstract

Abstract:
Nephrotic syndrome (NS) is the second most common cause of end-stage kidney disease (ESKD) before age
twenty-five. The spectrum of disease is defined by response to steroids, divided into steroid resistant nephrotic
syndrome (SRNS) and steroid sensitive nephrotic syndrome (SSNS). SRNS has limited therapeutic options and
often progresses to chronic kidney disease (CKD) and ESKD, while SSNS carries significant morbidity due to
long-term treatment with non-specific immunosuppression. We aim to improve our understanding of the genetic
drivers of NS to more precisely guide clinical management and create targeted therapies.
The past two decades have seen an increased understanding of the genetic basis of NS, particularly in the
discovery of Mendelian causes of NS. Mendelian forms of NS are primarily recessive, with two pathogenic
variants being essentially fully penetrant for the more severe form of NS, SRNS. The first recessive Mendelian
NS gene discovered was nephrin (NPHS1). In keeping with this inheritance model, the heterozygous state has
been thought to be clinically silent – a true “carrier” state. Recently, a published analysis of a Finnish population
cohort (FinnGen) challenged that model by showing that carriers of “Fin-Major”, a specific NPHS1 loss-of-
function Mendelian founder mutation in Finns, have increased odds of kidney disease. Additionally, genome
wide association studies (GWAS) have implicated common variants in NPHS1 with increased risk of SSNS,
reduced estimated glomerular filtration rate (eGFR), and lower serum albumin. Taken together, these
discoveries suggest that forms of genetic variation beyond bi-allelic Mendelian variants, such as heterozygous
rare pathogenic coding variants and common regulatory variants, may alter NPHS1 function and contribute to
kidney dysfunction and disease.
The overall goal of my project is to discover the association of coding and non-coding NPHS1 variants across the
allele frequency spectrum with diverse kidney diseases and traits. More specifically, I hypothesize that in the
general population, heterozygous, pathogenic Mendelian NPHS1 variants and common risk variants discovered
by GWAS are associated with lower eGFR, higher urine protein levels, and increased odds of nephrotic syndrome.
To test this hypothesis, I propose testing the following specific aims amongst 1.5 million people enrolled in
multiple large population- and hospital system-based biorepositories:
Aim 1: Discover the clinical consequences of Fin-Major carrier state in the FinnGen cohort.
Aim 2: Discover the prevalence and clinical impact of rare and common NPHS1 variants in 5
hospital based and population cohorts collectively totaling approximately 1,500,000 individuals.

## Key facts

- **NIH application ID:** 10998554
- **Project number:** 1F32DK141214-01
- **Recipient organization:** BOSTON CHILDREN'S HOSPITAL
- **Principal Investigator:** Adrian Olaf Banerji
- **Activity code:** F32 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $87,064
- **Award type:** 1
- **Project period:** 2024-07-17 → 2025-07-16

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10998554

## Citation

> US National Institutes of Health, RePORTER application 10998554, Discovering the Consequences of Genetic Variation in Nephrin on Kidney Diseases and Traits in Biobank Populations (1F32DK141214-01). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10998554. Licensed CC0.

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