SBIR-STTR Award

Non-Invasive Saliva-Based Diabetes Autoantibody Screening.
Award last edited on: 9/23/13

Sponsored Program
SBIR
Awarding Agency
NIH : NIDDK
Total Award Amount
$582,750
Award Phase
2
Solicitation Topic Code
-----

Principal Investigator
Srinivasa R Nagalla

Company Information

DiabetOmics LLC

2345 Northwest Amberbrook Drive Suite 140
Hillsboro, OR 97006
   (503) 924-5110
   info@diabetomics.com
   www.diabetomics.com
Location: Single
Congr. District: 01
County: Washington

Phase I

Contract Number: 1R43DK096956-01
Start Date: 9/5/12    Completed: 7/31/14
Phase I year
2012
Phase I Amount
$291,375
The presence of islet-directed auto-immunity and associated circulating auto-antibodies, previously thought to be primarily characteristic of type-1 diabetes mellitus (T1DM), is now apparent in a proportion of individuals with putative type-2 diabetes (T2DM), consistent with an increasing appreciation of diabetes as a continuous spectrum. Based on the observations that: 1) >98 percent of new-onset cases of T1DM have one or more auto-antibodies; 2) the number of auto-antibodies is proportional to risk of developing T1DM, with any one corresponding to an almost 30-fold increase in risk; 3) the presence of auto-antibodies in adolescents with apparent T2DM defines a distinct patient group that may require different treatment regimens; and 4) the presence of auto-antibodies in adults with presumed T2DM can indicate a more rapid progression to insulin dependency, increased screening for autoantibody status in diabetic and pre-diabetic populations is warranted. The major hurdle for reaching the large at-risk population is the lack of a simple-to-use, point-of-car device to rapidly screen for diabetes autoimmune status. The extension of accurate autoantibody detection to alternative body fluids can facilitate the accessibility of this importan diagnostic parameter to at-risk patient groups for more cost-effective and efficient disease detection and monitoring. Our preliminary data support the hypothesis that diabetes auto-antibodies can be reliably assessed in saliva and that their detection is amenable to simple point- of-care, device-based technologies. To demonstrate the utility of this approach, we will pursue the following two Specific Aims in this phase-I application. Specific aim 1: Correlation of autoantibody status in matched serum and saliva samples in classical T1DM and in T2DM. Specific aim 2: Development of a non-invasive, saliva-based, lateral-flow device for detection of autoimmune diabetes. The proposed research, by developing "new methods and technologies able to identify individuals at risk of developing type-1 diabetes" with a specific focus on point-f-care assays, low-cost/portable devices, non-invasive testing, and assessment of immune status, is directly relevant to the goals of RFA-DK-11-024 and many of the relevant topics described therein.

Public Health Relevance:
The incidence of diabetes is reaching epidemic proportions in the US and the world at large, with projected massive increases in the number of individuals with additional serious complications such as heart, kidney, and eye disease and cognitive decline. A significant problem is the lack of a simple, inexpensive, and convenient approach to detect persons with autoimmune diabetes. The ability to easily identify people that may be at risk for the development of autoimmune diabetes is critical to prevent acute, life-threatening conditions as well as to institute measures to delay or prevent the progression of the disease. The research proposed in this application will investigate the feasibility of measuring antibodies that reflect the risk of diabetes in saliva rather than in blood, and develop a simple non-invasive test device similar to a home pregnancy test that will be suitable for medical office, home, and field use to determine if one has the auto-antibodies that are associated with diabetes risk.

Public Health Relevance Statement:
The incidence of diabetes is reaching epidemic proportions in the US and the world at large, with projected massive increases in the number of individuals with additional serious complications such as heart, kidney, and eye disease and cognitive decline. A significant problem is the lack of a simple, inexpensive, and convenient approach to detect persons with autoimmune diabetes. The ability to easily identify people that may be at risk for the development of autoimmune diabetes is critical to prevent acute, life-threatening conditions as well as to institute measures to delay or prevent the progression of the disease. The research proposed in this application will investigate the feasibility of measuring antibodies that reflect the risk of diabetes in saliva rather than in blood, and develop a simple non-invasive test device similar to a home pregnancy test that will be suitable for medical office, home, and field use to determine if one has the auto-antibodies that are associated with diabetes risk.

NIH Spending Category:
Autoimmune Disease; Bioengineering; Clinical Research; Diabetes; Health Services; Nutrition; Obesity; Pediatric; Pediatric Research Initiative; Prevention

Project Terms:
Acute; Adolescent; Adult; Affect; Antibodies; Architecture; Autoantibodies; Autoimmune Diabetes; Autoimmune Process; Autoimmunity; base; Biological; Biological Assay; Biological Markers; Blood; Body Fluids; Caring; Categories; Characteristics; Chemistry; Chronic; Clinical; clinical practice; Clinical Research; cohort; commercialization; Complex; Consumption; cost; cost effective; Data; Dependency (Psychology); design; Detection; Development; Device or Instrument Development; Devices; Diabetes autoantibodies; Diabetes Mellitus; diabetes risk; diabetic; Diagnosis; Diagnostic; Disease; Disease Progression; Energy Metabolism; Enzyme-Linked Immunosorbent Assay; Epidemic; Exhibits; experience; Eye diseases; fetal; Foundations; Goals; Heart Diseases; HIV Antibodies; Home environment; Human Resources; IA-2-autoantibody; Immune; Immunity; Immunoassay; Impaired cognition; Incidence; Individual; Inflammation; Inflammatory; Institutes; Insulin; Insulin-Dependent Diabetes Mellitus; islet; Kidney Diseases; Laboratories; Lateral; Life; Liquid substance; Measures; Medical; Methods; Monitor; Non-Insulin-Dependent Diabetes Mellitus; Obesity; Patients; Persons; Phase; phase 2 study; point of care; Population; Populations at Risk; Pregnancy Tests; prevent; product development; public health medicine (field); Reference Standards; Research; research and development; Research Design; Resources; Risk; Saliva; saliva diagnostic; Sampling; Screening procedure; Serum; Siblings; Surface; Technology; Testing; Transportation; Treatment Protocols; vaginal fluid; Validation

Phase II

Contract Number: 5R43DK096956-02
Start Date: 9/5/12    Completed: 7/31/14
Phase II year
2013
Phase II Amount
$291,375
The presence of islet-directed auto-immunity and associated circulating auto-antibodies, previously thought to be primarily characteristic of type-1 diabetes mellitus (T1DM), is now apparent in a proportion of individuals with putative type-2 diabetes (T2DM), consistent with an increasing appreciation of diabetes as a continuous spectrum. Based on the observations that: 1) >98 percent of new-onset cases of T1DM have one or more auto-antibodies; 2) the number of auto-antibodies is proportional to risk of developing T1DM, with any one corresponding to an almost 30-fold increase in risk; 3) the presence of auto-antibodies in adolescents with apparent T2DM defines a distinct patient group that may require different treatment regimens; and 4) the presence of auto-antibodies in adults with presumed T2DM can indicate a more rapid progression to insulin dependency, increased screening for autoantibody status in diabetic and pre-diabetic populations is warranted. The major hurdle for reaching the large at-risk population is the lack of a simple-to-use, point-of-car device to rapidly screen for diabetes autoimmune status. The extension of accurate autoantibody detection to alternative body fluids can facilitate the accessibility of this importan diagnostic parameter to at-risk patient groups for more cost-effective and efficient disease detection and monitoring. Our preliminary data support the hypothesis that diabetes auto-antibodies can be reliably assessed in saliva and that their detection is amenable to simple point- of-care, device-based technologies. To demonstrate the utility of this approach, we will pursue the following two Specific Aims in this phase-I application. Specific aim 1: Correlation of autoantibody status in matched serum and saliva samples in classical T1DM and in T2DM. Specific aim 2: Development of a non-invasive, saliva-based, lateral-flow device for detection of autoimmune diabetes. The proposed research, by developing "new methods and technologies able to identify individuals at risk of developing type-1 diabetes" with a specific focus on point-f-care assays, low-cost/portable devices, non-invasive testing, and assessment of immune status, is directly relevant to the goals of RFA-DK-11-024 and many of the relevant topics described therein.

Public Health Relevance Statement:
The incidence of diabetes is reaching epidemic proportions in the US and the world at large, with projected massive increases in the number of individuals with additional serious complications such as heart, kidney, and eye disease and cognitive decline. A significant problem is the lack of a simple, inexpensive, and convenient approach to detect persons with autoimmune diabetes. The ability to easily identify people that may be at risk for the development of autoimmune diabetes is critical to prevent acute, life-threatening conditions as well as to institute measures to delay or prevent the progression of the disease. The research proposed in this application will investigate the feasibility of measuring antibodies that reflect the risk of diabetes in saliva rather than in blood, and develop a simple non-invasive test device similar to a home pregnancy test that will be suitable for medical office, home, and field use to determine if one has the auto-antibodies that are associated with diabetes risk.

Project Terms:
Acute; Adolescent; Adult; Affect; Antibodies; Architecture; Autoantibodies; Autoimmune Diabetes; Autoimmune Process; Autoimmunity; base; Biological; Biological Assay; Biological Markers; Blood; Body Fluids; Caring; Categories; Characteristics; Chemistry; Chronic; Clinical; clinical practice; Clinical Research; cohort; commercialization; Complex; Consumption; cost; cost effective; Data; Dependency (Psychology); design; Detection; Development; Device or Instrument Development; Devices; Diabetes autoantibodies; Diabetes Mellitus; diabetes risk; diabetic; Diagnosis; Diagnostic; Disease; Disease Progression; Energy Metabolism; Enzyme-Linked Immunosorbent Assay; Epidemic; Exhibits; experience; Eye diseases; fetal; Foundations; Goals; Heart Diseases; HIV Antibodies; Home environment; Human Resources; IA-2-autoantibody; Immune; Immunity; Immunoassay; Impaired cognition; Incidence; Individual; Inflammation; Inflammatory; Institutes; Insulin; Insulin-Dependent Diabetes Mellitus; islet; Kidney Diseases; Laboratories; Lateral; Life; Liquid substance; Measures; Medical; Methods; Monitor; Non-Insulin-Dependent Diabetes Mellitus; Obesity; Patients; Persons; Phase; phase 2 study; point of care; Population; Populations at Risk; Pregnancy Tests; prevent; product development; public health medicine (field); Reference Standards; Research; research and development; Research Design; Resources; Risk; Saliva; saliva diagnostic; Sampling; screening; Serum; Siblings; Surface; Technology; Testing; Transportation; Treatment Protocols; vaginal fluid; Validation