R01HL156024
Project Grant
Overview
Grant Description
MINOCYCLINE AS A POTENTIAL THERAPY FOR NEUROINFLAMMATION AND COGNITIVE DEFICIT IN SICKLE CELL DISEASE - PROJECT ABSTRACT
COGNITIVE AND BEHAVIORAL (ANXIETY AND DEPRESSION) DEFICITS ARE TWO POTENTIALLY LIFE-ALTERING COMPLICATIONS OF SICKLE CELL DISEASE (SCD). LOSS OF FULL-SCALE INTELLIGENCE QUOTIENT (IQ), INTERFERENCE WITH EMPLOYABILITY, NAVIGATION OF HEALTHCARE RESOURCES AND OVERALL QUALITY OF LIFE ARE SOME OF THE CONSEQUENCES OF COGNITIVE DEFICIT IN SCD PATIENTS.
THE MOLECULAR AND CELLULAR FACTORS THAT MEDIATE THE DEVELOPMENT OF THESE COMPLICATIONS ARE STILL LARGELY UNKNOWN. THIS PROPOSAL AIMS TO DEFINE THE ROLE OF NEUROINFLAMMATION IN DEVELOPMENT OF ABNORMAL NEUROPLASTICITY AND HOW THE TWO ARE TEMPORALLY RELATED TO ONSET OF COGNITIVE AND BEHAVIORAL DEFICIT IN SCD.
WE WILL ALSO ATTEMPT TO IDENTIFY SOME SMALL MOLECULES AND TREATMENT STRATEGIES THAT COULD HAVE UTILITY IN PREVENTION AND/OR TREATMENT OF SCD-ASSOCIATED COGNITIVE AND BEHAVIORAL DEFICIT.
OUR PRELIMINARY STUDIES HAVE SHOWN THAT SICKLE CELL MICE DEVELOPED COGNITIVE AND BEHAVIORAL DEFICIT THAT OCCUR WITH AGE AND NEUROINFLAMMATION AND THUS OUR CENTRAL HYPOTHESIS IS THAT THE DEVELOPMENT OF COGNITIVE DEFICITS IN SCD IS DUE TO NEUROINFLAMMATION AND ABNORMAL NEUROPLASTICITY DEFINED BY DECREASED DENSITY OF DENDRITIC ARBORS, DENDRITIC SPINES AND, THE PROPORTION OF IMMATURE DENDRITIC SPINES.
WE WILL ALSO EXAMINE THE POTENTIAL ROLE OR CONTRIBUTION FROM CEREBRAL INFARCTS AND MICROVASCULOPATHY. THIS WILL BE RIGOROUSLY TESTED WITH THE FOLLOWING AIMS:
(1) DETERMINE THE TEMPORAL RELATIONSHIP BETWEEN PRESENCE OF COGNITIVE (LEARNING AND MEMORY) DEFICIT IN SCD, AND ABNORMAL NEUROPLASTICITY AND/OR THE BURDEN OF CEREBRAL INFARCTS AND MICROVASCULOPATHY. THIS WILL ENABLE US TO ESTABLISH A TEMPORAL RELATIONSHIP BETWEEN THE ONSET OF COGNITIVE AND BEHAVIORAL DEFICIT, AND ONSET OF ABNORMAL NEUROPLASTICITY AS WELL AS THE BURDEN OF CEREBRAL MICROINFARCT.
(2) DEMONSTRATE THE ROLE OF NEUROINFLAMMATION, AS WELL AS THE THERAPEUTIC BENEFIT OF MINOCYCLINE IN TREATING COGNITIVE DEFICITS IN SCD. THIS WILL BE DONE BY ESTABLISHING BASELINE RELATIONSHIP BETWEEN ONSET AND PROGRESSION OF CELLULAR AND MOLECULAR EVIDENCE OF NEUROINFLAMMATION AND ONSET AND PROGRESSION OF ABNORMAL NEUROPLASTICITY AS WELL AS DEVELOPMENT OF COGNITIVE AND BEHAVIORAL DEFICIT. ADDITIONALLY, WE WILL EXAMINE WHETHER BLOCKING NEUROINFLAMMATION COULD BE A POTENTIAL TARGET FOR THE TREATMENT OR PREVENTION OF SCD ASSOCIATED COGNITIVE AND BEHAVIORAL DEFICIT.
(3) DETERMINE WHETHER TREATMENT WITH A NEUROTROPHIN AGONIST TREATMENT OR ANTI-NEUROINFLAMMATORY MEDIATORS REVERSES NEUROINFLAMMATION, ABNORMAL NEUROPLASTICITY AND COGNITIVE DEFICIT IN SCD.
THESE STUDIES ARE DESIGN TO ENABLE US IDENTIFY SMALL MOLECULE(S) AND/OR SMALL MOLECULE TARGET(S) AND PROVIDE THE PRECLINICAL INFORMATION THAT COULD SUPPORT A CLINICAL TRIAL GEARED TOWARDS IDENTIFYING TREATMENT AND PREVENTION STRATEGIES FOR COGNITIVE AND BEHAVIORAL DEFICIT IN SCD.
COGNITIVE AND BEHAVIORAL (ANXIETY AND DEPRESSION) DEFICITS ARE TWO POTENTIALLY LIFE-ALTERING COMPLICATIONS OF SICKLE CELL DISEASE (SCD). LOSS OF FULL-SCALE INTELLIGENCE QUOTIENT (IQ), INTERFERENCE WITH EMPLOYABILITY, NAVIGATION OF HEALTHCARE RESOURCES AND OVERALL QUALITY OF LIFE ARE SOME OF THE CONSEQUENCES OF COGNITIVE DEFICIT IN SCD PATIENTS.
THE MOLECULAR AND CELLULAR FACTORS THAT MEDIATE THE DEVELOPMENT OF THESE COMPLICATIONS ARE STILL LARGELY UNKNOWN. THIS PROPOSAL AIMS TO DEFINE THE ROLE OF NEUROINFLAMMATION IN DEVELOPMENT OF ABNORMAL NEUROPLASTICITY AND HOW THE TWO ARE TEMPORALLY RELATED TO ONSET OF COGNITIVE AND BEHAVIORAL DEFICIT IN SCD.
WE WILL ALSO ATTEMPT TO IDENTIFY SOME SMALL MOLECULES AND TREATMENT STRATEGIES THAT COULD HAVE UTILITY IN PREVENTION AND/OR TREATMENT OF SCD-ASSOCIATED COGNITIVE AND BEHAVIORAL DEFICIT.
OUR PRELIMINARY STUDIES HAVE SHOWN THAT SICKLE CELL MICE DEVELOPED COGNITIVE AND BEHAVIORAL DEFICIT THAT OCCUR WITH AGE AND NEUROINFLAMMATION AND THUS OUR CENTRAL HYPOTHESIS IS THAT THE DEVELOPMENT OF COGNITIVE DEFICITS IN SCD IS DUE TO NEUROINFLAMMATION AND ABNORMAL NEUROPLASTICITY DEFINED BY DECREASED DENSITY OF DENDRITIC ARBORS, DENDRITIC SPINES AND, THE PROPORTION OF IMMATURE DENDRITIC SPINES.
WE WILL ALSO EXAMINE THE POTENTIAL ROLE OR CONTRIBUTION FROM CEREBRAL INFARCTS AND MICROVASCULOPATHY. THIS WILL BE RIGOROUSLY TESTED WITH THE FOLLOWING AIMS:
(1) DETERMINE THE TEMPORAL RELATIONSHIP BETWEEN PRESENCE OF COGNITIVE (LEARNING AND MEMORY) DEFICIT IN SCD, AND ABNORMAL NEUROPLASTICITY AND/OR THE BURDEN OF CEREBRAL INFARCTS AND MICROVASCULOPATHY. THIS WILL ENABLE US TO ESTABLISH A TEMPORAL RELATIONSHIP BETWEEN THE ONSET OF COGNITIVE AND BEHAVIORAL DEFICIT, AND ONSET OF ABNORMAL NEUROPLASTICITY AS WELL AS THE BURDEN OF CEREBRAL MICROINFARCT.
(2) DEMONSTRATE THE ROLE OF NEUROINFLAMMATION, AS WELL AS THE THERAPEUTIC BENEFIT OF MINOCYCLINE IN TREATING COGNITIVE DEFICITS IN SCD. THIS WILL BE DONE BY ESTABLISHING BASELINE RELATIONSHIP BETWEEN ONSET AND PROGRESSION OF CELLULAR AND MOLECULAR EVIDENCE OF NEUROINFLAMMATION AND ONSET AND PROGRESSION OF ABNORMAL NEUROPLASTICITY AS WELL AS DEVELOPMENT OF COGNITIVE AND BEHAVIORAL DEFICIT. ADDITIONALLY, WE WILL EXAMINE WHETHER BLOCKING NEUROINFLAMMATION COULD BE A POTENTIAL TARGET FOR THE TREATMENT OR PREVENTION OF SCD ASSOCIATED COGNITIVE AND BEHAVIORAL DEFICIT.
(3) DETERMINE WHETHER TREATMENT WITH A NEUROTROPHIN AGONIST TREATMENT OR ANTI-NEUROINFLAMMATORY MEDIATORS REVERSES NEUROINFLAMMATION, ABNORMAL NEUROPLASTICITY AND COGNITIVE DEFICIT IN SCD.
THESE STUDIES ARE DESIGN TO ENABLE US IDENTIFY SMALL MOLECULE(S) AND/OR SMALL MOLECULE TARGET(S) AND PROVIDE THE PRECLINICAL INFORMATION THAT COULD SUPPORT A CLINICAL TRIAL GEARED TOWARDS IDENTIFYING TREATMENT AND PREVENTION STRATEGIES FOR COGNITIVE AND BEHAVIORAL DEFICIT IN SCD.
Awardee
Funding Goals
TO FOSTER HEART AND VASCULAR RESEARCH IN THE BASIC, TRANSLATIONAL, CLINICAL AND POPULATION SCIENCES, AND TO FOSTER TRAINING TO BUILD TALENTED YOUNG INVESTIGATORS IN THESE AREAS, FUNDED THROUGH COMPETITIVE RESEARCH TRAINING GRANTS. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, USE SMALL BUSINESS TO MEET FEDERAL RESEARCH AND DEVELOPMENT NEEDS, FOSTER AND ENCOURAGE PARTICIPATION IN INNOVATION AND ENTREPRENEURSHIP BY SOCIALLY AND ECONOMICALLY DISADVANTAGED PERSONS, AND INCREASE PRIVATE-SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT FUNDING. SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, FOSTER TECHNOLOGY TRANSFER THROUGH COOPERATIVE R&D BETWEEN SMALL BUSINESSES AND RESEARCH INSTITUTIONS, AND INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL R&D.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Cincinnati,
Ohio
452210001
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 568% from $552,583 to $3,692,658.
Cincinnati Univ Of was awarded
Minocycline Therapy for Cognitive Deficit in Sickle Cell Disease
Project Grant R01HL156024
worth $3,692,658
from National Heart Lung and Blood Institute in December 2020 with work to be completed primarily in Cincinnati Ohio United States.
The grant
has a duration of 5 years and
was awarded through assistance program 93.837 Cardiovascular Diseases Research.
The Project Grant was awarded through grant opportunity Research Project Grant (Parent R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 11/20/24
Period of Performance
12/15/20
Start Date
11/30/25
End Date
Funding Split
$3.7M
Federal Obligation
$0.0
Non-Federal Obligation
$3.7M
Total Obligated
Activity Timeline
Transaction History
Modifications to R01HL156024
Additional Detail
Award ID FAIN
R01HL156024
SAI Number
R01HL156024-1076227250
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75NH00 NIH NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
Funding Office
75NH00 NIH NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
Awardee UEI
DZ4YCZ3QSPR5
Awardee CAGE
2W614
Performance District
OH-01
Senators
Sherrod Brown
J.D. (James) Vance
J.D. (James) Vance
Budget Funding
Federal Account | Budget Subfunction | Object Class | Total | Percentage |
---|---|---|---|---|
National Heart, Lung, and Blood Institute, National Institutes of Health, Health and Human Services (075-0872) | Health research and training | Grants, subsidies, and contributions (41.0) | $1,477,250 | 100% |
Modified: 11/20/24