SBIR-STTR Award

A Saliva Based Epigenetic Assay for Assessing Vitamin B9 and B12 Status
Award last edited on: 4/10/2023

Sponsored Program
SBIR
Awarding Agency
NIH : NIA
Total Award Amount
$281,362
Award Phase
1
Solicitation Topic Code
866
Principal Investigator
Robert A Philibert

Company Information

Behavioral Diagnostics Inc

15 Prospect Place
Iowa City, IA 52246
   (319) 358-8602
   N/A
   N/A
Location: Single
Congr. District: 01
County: Johnson

Phase I

Contract Number: 1R43AG078082-01A1
Start Date: 9/1/2022    Completed: 10/31/2023
Phase I year
2022
Phase I Amount
$281,362
Gene-diet interactions can have major effects on human development, aging and response to medicaltherapy. In particular, this is true for key nutrients such as Vitamin A, D, B9 and B12. Unfortunately, the current"one size fits all" approaches for determining whether an individual has adequate levels of these and othermicronutrients relies on older studies that use serum assays that only capture recent intake that do not capturethe health care challenges incurred by our now aging, more diverse population We believe that integrated genetic-epigenetic assessments of saliva DNA can better capture cellularmicronutrient status and serve as a cornerstone of future Precision NutriEpigenomic therapies. Our method,which does not require drawing blood, will be robust against day-to-day dietary intake fluctuations and can beconducted using remote, telemedicine type approaches. This more functionally oriented method could findwidespread use in a variety of both medical and non-medical nutraceutical settings in optimizing athleticperformance, facilitating healthy aging and monitoring nutritional supplemental of both chronic (e.g., digestivedisease) and acute (e.g., chemotherapy) patients. For example, the method is generalized for the assessmentstargeting the use of common supplements such as Nicotinamide Adenine Dinucleotide (NAD+). We hypothesize that integrated genetic-epigenetic signatures of saliva DNA will robustly predict serum B9and B12 levels. To test that hypothesis, we will use data from a cohort of 450 African Americans for whom wealready have serum, genome wide genetic, and genome wide epigenetic data from whole blood DNA. We willuse machine learning to first mine the most predictive biosignature for serum B9 and B12 levels. Next, using ourpatent-pending, proprietary techniques, we will translate that whole blood (WB) DNA based signature into asaliva-based signature. Then, we will transform the test into an easy to perform set of methylation sensitivedigital PCR assays. If successful, the project will have high impact because it could lead to painless, at-home nutraceuticaltesting. It is significant because certain nutrients are thought to be protective against cancer or prematureaging. Our plan is highly feasible because the large body of prior work, abundant biomaterials, and ourexpertise in both epigenetics and machine learning. It is innovative because saliva diagnostics have not yetbeen introduced to the nutraceutical market. The BD team is well qualified. The project will led by Dr. RobPhilibert, an expert in epigenetic diagnostics. He will be assisted by a team of co-investigators that includesexperts in nutrition (Dr. Ruth Grossman) and biostatistics (Dr. Jeff Long). If successful, this R43 will serve asthe basis for an R44 that develop a battery of saliva based nutritional assays.

Public Health Relevance Statement:
Narrative The purpose of this grant is to determine whether saliva based epigenetic assays can be used to predict vitamin B9 and B12 levels. If successful, the technique could be used to painlessly and more effectively assess nutritional status.

Project Terms:

Phase II

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Start Date: 00/00/00    Completed: 00/00/00
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