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Completed SBIR-STTR RPGS NIH (US)

Single telomere length analysis using DNA array and FISH: a low-cost and accurate test for telomere-associated diseases

$4.49M USD

Funder NATIONAL INSTITUTE ON AGING
Recipient Organization Telohealthdx Llc
Country United States
Start Date Sep 25, 2024
End Date Aug 31, 2025
Duration 340 days
Number of Grantees 2
Roles Co-Investigator; Principal Investigator
Data Source NIH (US)
Grant ID 10816046
Grant Description

ABSTRACT Telomere-associated diseases, including telomere biology disorders (TBD), are prevalent among the aging population. TBD represent a group of most common premature aging syndromes, including dyskeratosis congenita (DC), aplastic anemia, and idiopathic pulmonary fibrosis (IPF), etc. The diagnosis of TBDs can be challenge due to the variable, complex, and time-dependent nature of

clinical manifestations. Genetic testing may be inconclusive because a significant portion of patients do not have an identifiable genetic cause. Telomere length testing has been shown to aid in DC diagnostics. However, a low-cost and accurate telomere length test is not available as a first line diagnostic or screening tool for the early detection of TBDs and other telomere-associated diseases.

We propose to develop a DNA array and fluorescent in situ hybridization (FISH)-based method to measure the absolute lengths of individual telomeres. The goal is to develop a low-cost, accurate, and high-throughput telomere test that uses a small amount of DNA, thus the test will be applicable to any cell/tissue type which DNA can be extracted from. This next-generation telomere test not only

measures average telomere length, but also telomere length distribution, thus providing a detailed telomere length profile for a patient. We anticipate that additional details in telomere length distribution will enhance the diagnostic accuracy of telomere-associated diseases because it is well documented that accumulation of critically short telomeres during aging or by environmental assaults

is responsible for the telomere-driven pathologies. In this phase I study, we propose the following two aims: 1) validate the optimized experimental conditions for accuracy in the measurement of telomere length; 2) determine the impact of DNA extraction methods on telomere length measurement. Phase I aims will lay the foundation for the Phase II study which will establish a new, accurate,

low-cost, and high-throughput telomere length assay and generate a marketable telomere diagnostic test to enhance the diagnosis and management of telomere-associated diseases. Given the rapid increase in the aging population and the relevance of telomere biology in human aging-related diseases, we anticipate the potential market for the test will be large.

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Telohealthdx Llc

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