R01HD116714
Project Grant
Overview
Grant Description
Targeting interindividual variability in NSAID responses to mitigate chronic pelvic pain risk in dysmenorrhea.
Menstrual pain (dysmenorrhea) is a major cause of distress, disability, and development of chronic pelvic pain (CPP).
Very little is known about how local uterine inflammation and central neural dysregulation interact to cause painful periods.
Understanding their interaction and how it might worsen central neural hypersensitivity is essential to prevent dysmenorrhea from progressing into CPP conditions like bladder pain syndrome, irritable bowel syndrome, or endometriosis.
There are two factors in dysmenorrhea we have studied that hold promise as targets to reduce future risk of CPP – the presence of co-occurring bladder hypersensitivity and the individual response to common anti-inflammatory treatments.
The expansion of pain from one pelvic organ to nearby ones suggests sensory processing dysregulation in the spinal cord or brain.
Our preliminary data shows that effective NSAID therapy for dysmenorrhea may reduce future CPP risk by normalizing local nerve activation, inflammatory molecules in the uterine lining, and painful hypersensitivity in adjacent pelvic organs.
To distinguish the role of different sensory mechanisms in CPP progression, our interdisciplinary team will use a collection of validated sensory tasks involving mechanical, thermal, electrical stimulation and bladder filling.
Our proposal also pairs high-density electroencephalography with sensory testing to identify brain differences related to abnormal pain interpretation.
We plan to administer these tasks along with symptom questionnaires to understand why some women with menstrual pain respond better to NSAIDs, and which factors predict diminished CPP risk following an optimized program to reduce menstrual pain.
In Aim 1 we will conduct a one-year, randomized controlled trial (N=300) of optimized NSAID vs. placebo treatment for period pain in moderate-plus dysmenorrhea sufferers.
We will determine whether active treatment, menstrual pain relief, and lower levels of uterine inflammatory molecules predict lower nonmenstrual pelvic pain (NMPP, a marker for future CPP risk) at one year post-treatment.
Aim 2, conducted within the Aim 1 study structure, will establish which specific sensory tests predict reductions in NMPP following treatment.
EEG will be used to pinpoint precise mechanisms for differences in these sensory responses.
Collectively, this study of higher-risk women is designed to characterize how menstrual pain and bladder hypersensitivity interact to promote CPP, and if these factors predict who benefits from early preventative treatment.
The approach is novel for using a sample of women enriched for future pain risk (women with dysmenorrhea and bladder pain) and for conducting future pain-risk prediction with recognized factors: sensory testing profiles, adjacent organ pain involvement, and observed response to a targeted treatment.
Structural equation modeling will be used to formally define how these interact to cause CPP while controlling for other key pain risk factors, such as relative local inflammation and psychosocial profiles.
These study results obtained by a diverse team of interdisciplinary collaborators are expected to markedly improve our understanding of pain risk heterogeneity for chronic pain prevention.
Menstrual pain (dysmenorrhea) is a major cause of distress, disability, and development of chronic pelvic pain (CPP).
Very little is known about how local uterine inflammation and central neural dysregulation interact to cause painful periods.
Understanding their interaction and how it might worsen central neural hypersensitivity is essential to prevent dysmenorrhea from progressing into CPP conditions like bladder pain syndrome, irritable bowel syndrome, or endometriosis.
There are two factors in dysmenorrhea we have studied that hold promise as targets to reduce future risk of CPP – the presence of co-occurring bladder hypersensitivity and the individual response to common anti-inflammatory treatments.
The expansion of pain from one pelvic organ to nearby ones suggests sensory processing dysregulation in the spinal cord or brain.
Our preliminary data shows that effective NSAID therapy for dysmenorrhea may reduce future CPP risk by normalizing local nerve activation, inflammatory molecules in the uterine lining, and painful hypersensitivity in adjacent pelvic organs.
To distinguish the role of different sensory mechanisms in CPP progression, our interdisciplinary team will use a collection of validated sensory tasks involving mechanical, thermal, electrical stimulation and bladder filling.
Our proposal also pairs high-density electroencephalography with sensory testing to identify brain differences related to abnormal pain interpretation.
We plan to administer these tasks along with symptom questionnaires to understand why some women with menstrual pain respond better to NSAIDs, and which factors predict diminished CPP risk following an optimized program to reduce menstrual pain.
In Aim 1 we will conduct a one-year, randomized controlled trial (N=300) of optimized NSAID vs. placebo treatment for period pain in moderate-plus dysmenorrhea sufferers.
We will determine whether active treatment, menstrual pain relief, and lower levels of uterine inflammatory molecules predict lower nonmenstrual pelvic pain (NMPP, a marker for future CPP risk) at one year post-treatment.
Aim 2, conducted within the Aim 1 study structure, will establish which specific sensory tests predict reductions in NMPP following treatment.
EEG will be used to pinpoint precise mechanisms for differences in these sensory responses.
Collectively, this study of higher-risk women is designed to characterize how menstrual pain and bladder hypersensitivity interact to promote CPP, and if these factors predict who benefits from early preventative treatment.
The approach is novel for using a sample of women enriched for future pain risk (women with dysmenorrhea and bladder pain) and for conducting future pain-risk prediction with recognized factors: sensory testing profiles, adjacent organ pain involvement, and observed response to a targeted treatment.
Structural equation modeling will be used to formally define how these interact to cause CPP while controlling for other key pain risk factors, such as relative local inflammation and psychosocial profiles.
These study results obtained by a diverse team of interdisciplinary collaborators are expected to markedly improve our understanding of pain risk heterogeneity for chronic pain prevention.
Funding Goals
TO CONDUCT AND SUPPORT LABORATORY RESEARCH, CLINICAL TRIALS, AND STUDIES WITH PEOPLE THAT EXPLORE HEALTH PROCESSES. NICHD RESEARCHERS EXAMINE GROWTH AND DEVELOPMENT, BIOLOGIC AND REPRODUCTIVE FUNCTIONS, BEHAVIOR PATTERNS, AND POPULATION DYNAMICS TO PROTECT AND MAINTAIN THE HEALTH OF ALL PEOPLE. TO EXAMINE THE IMPACT OF DISABILITIES, DISEASES, AND DEFECTS ON THE LIVES OF INDIVIDUALS. WITH THIS INFORMATION, THE NICHD HOPES TO RESTORE, INCREASE, AND MAXIMIZE THE CAPABILITIES OF PEOPLE AFFECTED BY DISEASE AND INJURY. TO SPONSOR TRAINING PROGRAMS FOR SCIENTISTS, DOCTORS, AND RESEARCHERS TO ENSURE THAT NICHD RESEARCH CAN CONTINUE. BY TRAINING THESE PROFESSIONALS IN THE LATEST RESEARCH METHODS AND TECHNOLOGIES, THE NICHD WILL BE ABLE TO CONDUCT ITS RESEARCH AND MAKE HEALTH RESEARCH PROGRESS UNTIL ALL CHILDREN, ADULTS, FAMILIES, AND POPULATIONS ENJOY GOOD HEALTH. THE MISSION OF THE NICHD IS TO ENSURE THAT EVERY PERSON IS BORN HEALTHY AND WANTED, THAT WOMEN SUFFER NO HARMFUL EFFECTS FROM REPRODUCTIVE PROCESSES, AND THAT ALL CHILDREN HAVE THE CHANCE TO ACHIEVE THEIR FULL POTENTIAL FOR HEALTHY AND PRODUCTIVE LIVES, FREE FROM DISEASE OR DISABILITY, AND TO ENSURE THE HEALTH, PRODUCTIVITY, INDEPENDENCE, AND WELL-BEING OF ALL PEOPLE THROUGH OPTIMAL REHABILITATION.
Grant Program (CFDA)
Place of Performance
Illinois
United States
Geographic Scope
State-Wide
Endeavor Health Clinical Operations was awarded
NSAID Response Variability in Dysmenorrhea: Mitigating Chronic Pelvic Pain Risk
Project Grant R01HD116714
worth $3,077,376
from the National Institute of Neurological Disorders and Stroke in September 2024 with work to be completed primarily in Illinois United States.
The grant
has a duration of 3 years and
was awarded through assistance program 93.279 Drug Abuse and Addiction Research Programs.
The Project Grant was awarded through grant opportunity HEAL Initiative: Understanding Individual Differences in Human Pain Conditions (R01 - Clinical Trial Optional).
Status
(Ongoing)
Last Modified 3/5/25
Period of Performance
9/17/24
Start Date
8/31/27
End Date
Funding Split
$3.1M
Federal Obligation
$0.0
Non-Federal Obligation
$3.1M
Total Obligated
Activity Timeline
Transaction History
Modifications to R01HD116714
Additional Detail
Award ID FAIN
R01HD116714
SAI Number
R01HD116714-934019844
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Nonprofit With 501(c)(3) IRS Status (Other Than An Institution Of Higher Education)
Awarding Office
75NT00 NIH Eunice Kennedy Shriver National Institute of Child Health & Human Development
Funding Office
75NQ00 NIH National Institute of Neurological Disorders and Stroke
Awardee UEI
MBKKNQM9QME3
Awardee CAGE
3EC10
Performance District
IL-90
Senators
Richard Durbin
Tammy Duckworth
Tammy Duckworth
Modified: 3/5/25