Liabilities / Assets
Score unavailable
Liabilities-to-assets requires both liabilities and assets on the latest valid filing.
EIN 45-2206152 • 501(c)3 • Nashville, TN
Profile
To carry out and support basic research related to Obsessive Compulsive Disorder OCD and Depression.
Precomputed percentiles relative to similar nonprofits. These scores are descriptive rather than judgmental.
Liabilities / Assets
Score unavailable
Liabilities-to-assets requires both liabilities and assets on the latest valid filing.
Liabilities / Revenue
Score unavailable
Liabilities-to-revenue requires both liabilities and revenue on the latest valid filing.
Net Margin
Score unavailable
Net margin requires both revenue and expenses on the latest valid filing.
Top Officer Pay
81st percentile
Higher top officer pay than 81% of similar nonprofits.
Asset Growth
10th percentile
Faster asset growth than 10% of similar nonprofits.
Revenue Growth
Score unavailable
A valid growth rate could not be computed from the available filing history.
Assets
Down$0
Down $39,682 (-100%) from 2022
Liabilities
-
No earlier filing loaded for comparison.
Net Assets
Down$0
Down $39,682 (-100%) from 2022
Revenue
Down$0
Down $300,000 (-100%) from 2022
Expenses
Down$1,200
Down $306,475 (-100%) from 2022
Net Income
Up-$1,200
Up $6,475 (+84%) from 2022
Most recent year
2025 • Form 990EZDetailed filing. Detailed filing data is available for this year.
To carry out and support research related to Obsessive Compulsive Disorder OCD and Depression.
To carry out and support basic research related to Obsessive Compulsive Disorder OCD and Depression.
| Description | Grants | Expenses |
|---|---|---|
| OCD AND DEPRESSION ARE EMOTIONALLY DEVASTATING PSYCHIATRIC DISORDERS WITH SIGNIFICANT SOCIAL AND ECONOMIC COSTS. AN ESTIMATED 5 TO 6 MILLION PEOPLE IN THE UNITED STATES WILL SUFFER FROM OCD DURING THEIR LIFETIME. THE WORLD HEALTH ORGANIZATION HAS SAID THAT OCD IS AMONG THE 10 MOST DISABLING CONDITIONS IN THE WORLD. ONE PROBLEM IS THAT THE MEDICATIONS USED TO TREAT OCD CAN TAKE UP TO TWELVE WEEKS TO EXERT THEIR EFFECT, AND ONLY 30 PERCENT OF PATIENTS WILL RESPOND TO THEIR FIRST MEDICATION TRIAL. THIS MEANS THAT THOSE WHO DO NOT RESPOND MUST WAIT ANOTHER 12 WEEKS TO SEE IF THE SECOND MEDICATION HAS ANY BENEFIT. IT IS NOT UNCOMMON FOR PATIENTS TO HAVE 3-4 MEDICATION TRIALS TO FIND A TREATMENT THAT WORKS. PATIENTS WITH EXTREME SYMPTOMS MAY GIVE UP AND TAKE THEIR LIVES. IN FACT, 14-17 PERCENT OF OCD PATIENTS WILL ATTEMPT SUICIDE DURING THEIR LIFETIME. AN ESTIMATED 17-20 MILLION AMERICAN ADULTS WILL SUFFER FROM DEPRESSION EACH YEAR. SEVERELY DEPRESSED PATIENTS ALSO HAVE HIGH SUICIDE RATES. SUICIDE IS THE FIFTH LEADING CAUSE OF DEATH AMONG ADULT MALES, AND IS THE THIRD LEADING CAUSE OF DEATH FOR ALL YOUNG PEOPLE AGES 15-24. ONE REASON FOR THESE HIGH SUICIDE RATES IS THAT SIGNIFICANT PERCENTAGES OF PATIENTS WITH OCD AND DEPRESSION WILL NOT RESPOND TO TREATMENTS, IN PART BECAUSE WE DO NOT UNDERSTAND WHAT REALLY CAUSES THESE DISORDERS. THE IFPN HAS FUNDED RESEARCH RELATED TO THE NEUROBIOLOGY OF DEPRESSION IN THE PAST, AND MAINTAINED AN IN-HOUSE RESEARCH LABORATORY PROGRAM COMPLETING STUDIES ON THE NEUROBIOLOGY OF OCD THAT ORIGINATED AT VANDERBILT UNIVERSITY MEDICAL CENTER. OUR IN-HOUSE RESEARCH HAS BEEN A CONTINUATION OF WORK CARRIED OUT BY THE FOUNDER THAT WAS FUNDED THROUGH THE DEPARTMENT OF PSYCHIATRY AT VANDERBILT UNIVERSITY MEDICAL CENTER. WHILE SCIENTISTS ARE AWARE THAT A SPECIFIC CIRCUIT IN THE BRAIN INVOLVING THE PREFRONTAL CORTEX MAY BE INVOLVED IN THE PATHOPHYSIOLOGY OF OCD, WE DO NOT UNDERSTAND WHY THIS CIRCUIT IS ABERRANT, WHY MEDICATIONS KNOWN AS SELECTIVE SEROTONIN REUPTAKE INHIBITORS, OR SSRI'S, THAT BLOCK THE INACTIVATION OF A NEUROTRANSMITTER CALLED SEROTONIN, ARE EFFECTIVE IN THE TREATMENT OF OCD, AND WHY PATIENTS MUST TAKE THESE MEDICATIONS FOR UP TO 12 WEEKS TO GET BENEFIT FROM THEM. THE PURPOSE OF THE PROGRAM WAS TO SHOW HOW SSRIS CHANGE THE ACTIVITY OF NERVE CELLS IN THE PREFRONTAL CORTEX SO THAT MORE TARGETED DRUG TREATMENTS MIGHT BE DEVELOPED THAT COULD NORMALIZE ACTIVITY IN THE OCD CIRCUIT AND REDUCE THE AMOUNT OF TIME THAT PATIENTS HAVE TO SUFFER, WAITING FOR THEIR SSRI TREATMENTS TO HAVE A BENEFIT. SUCH TARGETED MEDICATIONS COULD GREATLY IMPROVE THE TREATMENT AND QUALITY OF LIFE FOR THOSE SUFFERING FROM OCD. WE ATTEMPTED TO DETERMINE HOW THESE MEDICATIONS AFFECT THE OCD CIRCUIT USING AN ANIMAL MODEL IN WHICH WE STIMULATED SEROTONIN SIGNALING IN THE BRAIN. WE WANTED TO DETERMINE HOW DIFFERENT CELLS IN THE EMOTIONAL PREFRONTAL CORTEX RESPONDED TO INCREASED SEROTONIN STIMULATION. WE CHEMICALLY STIMULATED SEROTONIN RELEASE IN THE PREFRONTAL CORTEX THEN DETERMINED THE NUMBER OF NERVE CELLS THAT WERE SEROTONIN-ACTIVATED BY STAINING BRAIN SECTIONS FOR A PROTEIN CALLED FOS, THAT IS ASSOCIATED WITH NEURONAL ACTIVATION. WE WANTED TO DETERMINE HOW THAT ACTIVATION WAS AFFECTED BY SHORT-OR LONG-TERM SSRI TREATMENT. A PRELIMINARY STUDY FOUND THAT LONG TERM- BUT NOT SHORT-TERM SSRI TREATMENT DAMPENED PREFRONTAL-STIMULATED NEURONAL ACTIVITY. WE ALSO WANTED TO DETERMINE HOW DIFFERENT CELL TYPES IN THE PREFRONTAL CORTEX RESPONDED TO SEROTONIN STIMULATION, AND HOW THOSE RESPONSES WERE ALTERED BY SSRI TREAMENTS. IN OUR PRELIMINARY WORK WE FOUND THAT SEROTONIN AFFECTS THE PROCESSING NEURONS WITHIN THE PREFRONTAL CORTEX DIFFERENTLY THAN THEY AFFECT NEURONS THAT PROJECT FROM THE PREFRONTAL CORTEX TO OTHER BRAIN REGIONS. MORE RECENT ANALYSES HAVE RAISED QUESTIONS ABOUT THESE INITIAL FINDINGS. UNFORTUNATELY, OUR MOST IMPORTANT EXPERIMENT, A LARGE DEFINITIVE EXPERIMENT DESIGNED TO ADDRESS THESE QUESTIONS FAILED DUE TO AN INABILITY TO DETECT FOS PROTEIN IN THE BRAIN SECTIONS ABOVE BACKGROUND LEVELS OF STAINING. THE DATA THAT WE DO HAVE IS BEING ANALYZED TO DETERMINE IF THERE ARE ANY FINDINGS FROM THE STUDY THAT MIGHT BE PUBLISHABLE. ALL LABORATORY WORK ON ALL PROJECTS ENDED LAST FISCAL YEAR. THE LABORATORY IS NOW CLOSED AND THE INSTITUTE DISSOLVED LAST JULY. | - | $1,200 |
| Name | Title | Full / Part Time | Base | Other | Total |
|---|---|---|---|---|---|
| William A Hewlett | Executive Director | - | $0 | - | - |
| John H Sullivan | Secretary | - | $0 | - | - |
| Roger A Warnke | Treasurer | - | $0 | - | - |
“While there was no contractual relationship with vanderbilt university hospital, the institute for psychiatric neuroscience has been completing ocd-related research that was initiated and carried out at vanderbilt university medical, center for 13 years and provdied financial support for depression research at the medical center for a number of years. No grants were made to the medical center over the 2024-25 fiscal year.”
This appendix keeps the raw XML leaves available for debugging and edge-case review. The human report above is the primary experience.
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| IRS990EZ/ProgramSrvcAccomplishmentGrp/DescriptionProgramSrvcAccomTxt | 0 | OCD AND DEPRESSION ARE EMOTIONALLY DEVASTATING PSYCHIATRIC DISORDERS WITH SIGNIFICANT SOCIAL AND ECONOMIC COSTS. AN ESTIMATED 5 TO 6 MILLION PEOPLE IN THE UNITED STATES WILL SUFFER FROM OCD DURING THEIR LIFETIME. THE WORLD HEALTH ORGANIZATION HAS SAID THAT OCD IS AMONG THE 10 MOST DISABLING CONDITIONS IN THE WORLD. ONE PROBLEM IS THAT THE MEDICATIONS USED TO TREAT OCD CAN TAKE UP TO TWELVE WEEKS TO EXERT THEIR EFFECT, AND ONLY 30 PERCENT OF PATIENTS WILL RESPOND TO THEIR FIRST MEDICATION TRIAL. THIS MEANS THAT THOSE WHO DO NOT RESPOND MUST WAIT ANOTHER 12 WEEKS TO SEE IF THE SECOND MEDICATION HAS ANY BENEFIT. IT IS NOT UNCOMMON FOR PATIENTS TO HAVE 3-4 MEDICATION TRIALS TO FIND A TREATMENT THAT WORKS. PATIENTS WITH EXTREME SYMPTOMS MAY GIVE UP AND TAKE THEIR LIVES. IN FACT, 14-17 PERCENT OF OCD PATIENTS WILL ATTEMPT SUICIDE DURING THEIR LIFETIME. AN ESTIMATED 17-20 MILLION AMERICAN ADULTS WILL SUFFER FROM DEPRESSION EACH YEAR. SEVERELY DEPRESSED PATIENTS ALSO HAVE HIGH SUICIDE RATES. SUICIDE IS THE FIFTH LEADING CAUSE OF DEATH AMONG ADULT MALES, AND IS THE THIRD LEADING CAUSE OF DEATH FOR ALL YOUNG PEOPLE AGES 15-24. ONE REASON FOR THESE HIGH SUICIDE RATES IS THAT SIGNIFICANT PERCENTAGES OF PATIENTS WITH OCD AND DEPRESSION WILL NOT RESPOND TO TREATMENTS, IN PART BECAUSE WE DO NOT UNDERSTAND WHAT REALLY CAUSES THESE DISORDERS. THE IFPN HAS FUNDED RESEARCH RELATED TO THE NEUROBIOLOGY OF DEPRESSION IN THE PAST, AND MAINTAINED AN IN-HOUSE RESEARCH LABORATORY PROGRAM COMPLETING STUDIES ON THE NEUROBIOLOGY OF OCD THAT ORIGINATED AT VANDERBILT UNIVERSITY MEDICAL CENTER. OUR IN-HOUSE RESEARCH HAS BEEN A CONTINUATION OF WORK CARRIED OUT BY THE FOUNDER THAT WAS FUNDED THROUGH THE DEPARTMENT OF PSYCHIATRY AT VANDERBILT UNIVERSITY MEDICAL CENTER. WHILE SCIENTISTS ARE AWARE THAT A SPECIFIC CIRCUIT IN THE BRAIN INVOLVING THE PREFRONTAL CORTEX MAY BE INVOLVED IN THE PATHOPHYSIOLOGY OF OCD, WE DO NOT UNDERSTAND WHY THIS CIRCUIT IS ABERRANT, WHY MEDICATIONS KNOWN AS SELECTIVE SEROTONIN REUPTAKE INHIBITORS, OR SSRI'S, THAT BLOCK THE INACTIVATION OF A NEUROTRANSMITTER CALLED SEROTONIN, ARE EFFECTIVE IN THE TREATMENT OF OCD, AND WHY PATIENTS MUST TAKE THESE MEDICATIONS FOR UP TO 12 WEEKS TO GET BENEFIT FROM THEM. THE PURPOSE OF THE PROGRAM WAS TO SHOW HOW SSRIS CHANGE THE ACTIVITY OF NERVE CELLS IN THE PREFRONTAL CORTEX SO THAT MORE TARGETED DRUG TREATMENTS MIGHT BE DEVELOPED THAT COULD NORMALIZE ACTIVITY IN THE OCD CIRCUIT AND REDUCE THE AMOUNT OF TIME THAT PATIENTS HAVE TO SUFFER, WAITING FOR THEIR SSRI TREATMENTS TO HAVE A BENEFIT. SUCH TARGETED MEDICATIONS COULD GREATLY IMPROVE THE TREATMENT AND QUALITY OF LIFE FOR THOSE SUFFERING FROM OCD. WE ATTEMPTED TO DETERMINE HOW THESE MEDICATIONS AFFECT THE OCD CIRCUIT USING AN ANIMAL MODEL IN WHICH WE STIMULATED SEROTONIN SIGNALING IN THE BRAIN. WE WANTED TO DETERMINE HOW DIFFERENT CELLS IN THE EMOTIONAL PREFRONTAL CORTEX RESPONDED TO INCREASED SEROTONIN STIMULATION. WE CHEMICALLY STIMULATED SEROTONIN RELEASE IN THE PREFRONTAL CORTEX THEN DETERMINED THE NUMBER OF NERVE CELLS THAT WERE SEROTONIN-ACTIVATED BY STAINING BRAIN SECTIONS FOR A PROTEIN CALLED FOS, THAT IS ASSOCIATED WITH NEURONAL ACTIVATION. WE WANTED TO DETERMINE HOW THAT ACTIVATION WAS AFFECTED BY SHORT-OR LONG-TERM SSRI TREATMENT. A PRELIMINARY STUDY FOUND THAT LONG TERM- BUT NOT SHORT-TERM SSRI TREATMENT DAMPENED PREFRONTAL-STIMULATED NEURONAL ACTIVITY. WE ALSO WANTED TO DETERMINE HOW DIFFERENT CELL TYPES IN THE PREFRONTAL CORTEX RESPONDED TO SEROTONIN STIMULATION, AND HOW THOSE RESPONSES WERE ALTERED BY SSRI TREAMENTS. IN OUR PRELIMINARY WORK WE FOUND THAT SEROTONIN AFFECTS THE PROCESSING NEURONS WITHIN THE PREFRONTAL CORTEX DIFFERENTLY THAN THEY AFFECT NEURONS THAT PROJECT FROM THE PREFRONTAL CORTEX TO OTHER BRAIN REGIONS. MORE RECENT ANALYSES HAVE RAISED QUESTIONS ABOUT THESE INITIAL FINDINGS. UNFORTUNATELY, OUR MOST IMPORTANT EXPERIMENT, A LARGE DEFINITIVE EXPERIMENT DESIGNED TO ADDRESS THESE QUESTIONS FAILED DUE TO AN INABILITY TO D |
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| IRS990ScheduleA/Form990ScheduleAPartVIGrp/ExplanationTxt | 0 | WHILE THERE IS NO CONTRACTUAL RELATIONSHIP WITH VANDERBILT HOSPITAL, THE INSTITUTE FOR PSYCHIATRIC NEUROSCIENCE IS COMPLETING OCD-AND DEPRESSION-RELATED RESEARCH THAT WAS INITIATED AND CARRIED OUT FOR 13 YEARS AT VANDERBILT UNIVERSITY MEDICAL CENTER. THE IFPN ALSO PROVIDED FINANCIAL SUPPORT FOR DEPRESSION-RELATED RESEARCH AT THE MEDICAL CENTER FOR MANY YEARS IN THE PAST. NO GRANTS WERE MADE TO THE MEDICAL CENTER OVER THE 2023-24 FISCAL YEAR. |
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| IRS990ScheduleO/SupplementalInformationDetail/ExplanationTxt | 0 | WHILE THERE WAS NO CONTRACTUAL RELATIONSHIP WITH VANDERBILT UNIVERSITY HOSPITAL, THE INSTITUTE FOR PSYCHIATRIC NEUROSCIENCE HAS BEEN COMPLETING OCD-RELATED RESEARCH THAT WAS INITIATED AND CARRIED OUT AT VANDERBILT UNIVERSITY MEDICAL, CENTER FOR 13 YEARS AND PROVDIED FINANCIAL SUPPORT FOR DEPRESSION RESEARCH AT THE MEDICAL CENTER FOR A NUMBER OF YEARS. NO GRANTS WERE MADE TO THE MEDICAL CENTER OVER THE 2024-25 FISCAL YEAR. |
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