Opportunity Information: Apply for RFA DK 22 023

The NIH, through the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), offered this discretionary grant opportunity (RFA-DK-22-023) to support ancillary research projects that plug into the existing NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC). The scientific backdrop is that the IBDGC, working alongside the International IBD Genetics Consortium, has already mapped more than 250 genetic susceptibility loci linked to inflammatory bowel disease (IBD). Even with that progress, the field is still facing a major bottleneck: only a small fraction of those loci can be followed up with deeper functional work using current consortium resources, meaning most of the actual biological mechanisms behind the genetic signals remain unresolved. This FOA was designed to push beyond gene mapping and into the next stage of discovery by expanding how many loci, variants, genes, and IBD-relevant biological domains can be investigated using the consortiums established participants, biospecimens, and datasets.

At its core, the program aims to fund well-justified ancillary studies that leverage the IBDGC infrastructure to move from association to mechanism. Projects are expected to focus specifically on identifying causal variants within known IBD risk loci and/or functionally characterizing the effector genes that translate those variants into real biological effects. In practical terms, that typically means narrowing down which specific variants in a risk region are likely driving disease risk, linking those variants to changes in gene regulation or gene function, and then demonstrating how those changes impact relevant pathways or cell types involved in IBD pathophysiology and clinical course. The FOA also emphasizes broadening the scope of IBD phenotypes and physiological domains examined, consistent with the renewed mission of the IBDGC to clarify genetic architecture across diverse populations and to better understand how genetics influences disease features and outcomes, not just overall susceptibility.

A key boundary condition is that proposed ancillary studies must not duplicate work that the IBDGC is already conducting or has completed. The intention is to complement and extend the consortiums active portfolio rather than re-run overlapping analyses. The opportunity uses the R01 grant mechanism and is labeled "Clinical Trial Not Allowed," which signals that the funded work should be mechanistic, translational, genomic, computational, or laboratory-based in a way that does not meet NIHs definition of a clinical trial. Applicants are expected to design projects that make strong use of existing IBDGC resources, such as curated cohorts, genotype and phenotype datasets, and available biospecimens, rather than building an entirely independent patient recruitment enterprise.

From an administrative standpoint, the awarding agency is the National Institutes of Health, with the activity falling under CFDA 93.847 and categorized under food and nutrition and health. The award ceiling listed is $300,000, indicating the maximum amount that could be requested under the terms shown in the source information. The original closing date provided is 2023-11-08, and the FOA was created on 2022-12-23. While the source text does not specify the number of expected awards, it indicates that awards would be made under the NIH grant framework, with the usual competitive review considerations focused on significance, innovation, approach, investigators, and environment, plus fit to the consortium-based ancillary purpose.

Eligibility is broad and includes many standard applicant types such as public and private institutions of higher education, nonprofits (with or without 501(c)(3) status), for-profit organizations (other than small businesses), small businesses, and various levels of government (state, county, city or township, special district), as well as independent school districts and public housing authorities/Indian housing authorities. It also explicitly highlights additional eligible applicants and organizational categories, including Alaska Native and Native Hawaiian Serving Institutions, Asian American Native American Pacific Islander Serving Institutions (AANAPISIs), Historically Black Colleges and Universities (HBCUs), Hispanic-serving Institutions, Tribally Controlled Colleges and Universities (TCCUs), Indian/Native American tribal governments (other than federally recognized), non-U.S. entities (foreign organizations), U.S. territories or possessions, regional organizations, eligible federal agencies, and faith-based or community-based organizations. This breadth aligns with the FOAs emphasis on studying diverse populations and expanding the biological and phenotypic scope of IBD genetics research by encouraging participation across a wide range of institutions and communities.

Overall, this grant opportunity is best understood as a mechanism to accelerate post-GWAS discovery in IBD by funding targeted ancillary projects that use the IBDGCs established cohorts, samples, and data to pinpoint causal variants, identify and validate effector genes, and clarify the biological pathways linking genetics to IBD mechanisms and clinical behavior, while avoiding overlap with the consortiums ongoing or completed studies.

  • The National Institutes of Health in the food and nutrition, health sector is offering a public funding opportunity titled "Ancillary Studies to the NIDDK Inflammatory Bowel Disease Genetics Consortium (R01 Clinical Trial Not Allowed)" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.847.
  • This funding opportunity was created on 2022-12-23.
  • Applicants must submit their applications by 2023-11-08. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • Each selected applicant is eligible to receive up to $300,000.00 in funding.
  • Eligible applicants include: State governments, County governments, City or township governments, Special district governments, Independent school districts, Public and State controlled institutions of higher education, Native American tribal governments (Federally recognized), Public housing authorities/Indian housing authorities, Native American tribal organizations (other than Federally recognized tribal governments), Nonprofits having a 501 (c) (3) status with the IRS, other than institutions of higher education, Nonprofits that do not have a 501 (c) (3) status with the IRS, other than institutions of higher education, Private institutions of higher education, For-profit organizations other than small businesses, Small businesses, Others.
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FAQs: NIH/NIDDK RFA-DK-22-023 (IBDGC Ancillary Studies)

What is this funding opportunity?

This is an NIH discretionary grant opportunity from the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (FOA: RFA-DK-22-023). It supports ancillary research projects that connect to and leverage the existing NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC).

What is the main goal of the FOA?

The core goal is to move IBD genetics beyond association signals and toward biological mechanism. The FOA is designed to expand how many known IBD risk loci can be followed up with deeper functional work by using the consortium's established participants, biospecimens, and datasets.

Why is NIH focusing on ancillary studies for IBD genetics right now?

The IBDGC and the International IBD Genetics Consortium have identified more than 250 genetic susceptibility loci linked to inflammatory bowel disease. The current bottleneck is that only a small fraction of those loci can be investigated in depth with existing consortium resources, leaving most underlying biological mechanisms unresolved. This FOA aims to close that gap.

What kinds of studies are considered responsive to this FOA?

Responsive projects are well-justified ancillary studies that use the IBDGC infrastructure to (1) identify causal variants within known IBD risk loci and/or (2) functionally characterize effector genes that mediate the effects of those variants. Studies should leverage consortium resources rather than operate as fully independent efforts.

What does "move from association to mechanism" mean in this context?

It generally means narrowing a GWAS-implicated region to the specific variant(s) likely driving risk, connecting those variants to changes in gene regulation or gene function, and demonstrating how those changes affect IBD-relevant pathways, cell types, physiology, disease course, or outcomes.

Does the FOA focus only on identifying genes, or also on variants?

Both. The FOA emphasizes identifying causal variants within established IBD risk loci and functionally characterizing effector genes that translate genetic variation into biological effects.

Are projects expected to use the IBDGC cohorts, biospecimens, and datasets?

Yes. A central expectation is that proposed projects make strong use of existing IBDGC resources, including curated cohorts, genotype and phenotype datasets, and available biospecimens, rather than creating an entirely separate recruitment and data-collection enterprise.

Can an applicant propose work that overlaps with ongoing IBDGC projects?

No. A key requirement is that the ancillary study must not duplicate work the IBDGC is already conducting or has completed. The purpose is to complement and extend the consortium's portfolio, not repeat overlapping analyses.

Does this opportunity allow clinical trials?

No. The FOA is labeled "Clinical Trial Not Allowed," meaning the funded work should not meet NIH's definition of a clinical trial. The intended scope is mechanistic, translational, genomic, computational, and/or laboratory-based research that uses consortium resources without initiating a clinical trial.

What grant mechanism is used?

The opportunity uses the NIH R01 grant mechanism.

What is the maximum award amount listed?

The award ceiling provided is $300,000, which is the maximum amount indicated under the terms shown in the source information.

Who is the awarding agency?

The awarding agency is the National Institutes of Health (NIH), through NIDDK.

What CFDA number is associated with this opportunity?

The activity is listed under CFDA 93.847.

How is this opportunity categorized?

It is categorized under food and nutrition and health, consistent with NIDDK's mission area and the health focus of IBD genetics.

What is the application closing date listed in the source information?

The original closing date provided is 2023-11-08.

When was the FOA created?

The FOA was created on 2022-12-23.

Does the FOA specify how many awards NIH expects to make?

No. The source information does not specify the number of expected awards.

What review criteria apply to applications under this NIH opportunity?

The source indicates the usual NIH competitive review considerations, including significance, innovation, approach, investigators, and environment, along with fit to the consortium-based ancillary purpose of the FOA.

What types of organizations are eligible to apply?

Eligibility is broad and includes public and private institutions of higher education; nonprofits (with or without 501(c)(3) status); for-profit organizations (other than small businesses); small businesses; and multiple levels of government (state, county, city or township, special district). Independent school districts and public housing authorities/Indian housing authorities are also included.

Are minority-serving institutions specifically included in eligibility?

Yes. The FOA explicitly highlights eligibility for Alaska Native and Native Hawaiian Serving Institutions, Asian American Native American Pacific Islander Serving Institutions (AANAPISIs), Historically Black Colleges and Universities (HBCUs), Hispanic-serving Institutions, and Tribally Controlled Colleges and Universities (TCCUs).

Are tribal governments and community-based organizations eligible?

Yes. The eligibility list includes Indian/Native American tribal governments (other than federally recognized) and also includes faith-based or community-based organizations.

Are foreign organizations eligible to apply?

Yes. The FOA explicitly includes non-U.S. entities (foreign organizations) among eligible applicants.

Are U.S. territories or regional organizations eligible?

Yes. The eligibility list includes U.S. territories or possessions and regional organizations.

Are federal agencies eligible applicants under this FOA?

Yes. The source information includes eligible federal agencies among the eligible applicant categories.

What scientific areas or domains does NIH want to broaden through this FOA?

The FOA emphasizes broadening the scope of IBD phenotypes and physiological domains examined, aligned with the IBDGC's renewed mission to clarify genetic architecture across diverse populations and to better understand how genetics influences disease features and outcomes, not only disease susceptibility.

Does the FOA focus on diverse populations?

Yes. The program description ties the consortium mission to clarifying genetic architecture across diverse populations and expanding phenotypic and biological scope, and the eligibility breadth is consistent with encouraging participation across many institutions and communities.

What is the larger scientific context behind the FOA?

The backdrop is extensive locus discovery (over 250 susceptibility loci) paired with a functional follow-up bottleneck. This FOA is positioned as a mechanism to accelerate post-GWAS discovery by funding targeted ancillary projects that can pinpoint causal variants, identify and validate effector genes, and clarify pathways linking genetics to IBD mechanisms and clinical behavior.

What is the relationship between the IBDGC and the International IBD Genetics Consortium in this description?

The IBDGC is described as working alongside the International IBD Genetics Consortium to map IBD genetic susceptibility loci. This FOA specifically targets ancillary projects that plug into the NIDDK IBDGC infrastructure.

What is an "ancillary" study in the context of this FOA?

Based on the description provided, an ancillary study is a project that connects to the IBDGC and uses its existing cohorts, biospecimens, and datasets to answer additional mechanistic questions (especially variant and effector gene function) without duplicating ongoing or completed consortium work.

What kinds of outputs is NIH implicitly aiming for through these awards?

The FOA is geared toward outputs that clarify causality and function: identifying likely causal variants in known risk loci, linking them to regulatory or functional effects, identifying effector genes, and demonstrating how those effects influence IBD-relevant pathways, cell types, physiology, and clinical course or outcomes.

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