R01HL157533
Project Grant
Overview
Grant Description
Development of Clinical Prediction Models for Pulmonary Outcomes in Sarcoidosis - Project Abstract
The purpose of this proposal is to develop clinical prediction tools to risk stratify patients with pulmonary sarcoidosis. Because the course of sarcoidal inflammation lasts for many years even in those with self-limiting sarcoid, the lack of prognostic indicators upon which to develop a management plan is not a trivial issue for both patient and physician.
Thus, without prognostication tools, clinicians will not be able to improve the longitudinal care they provide for the types of outcomes that are used in the clinic. The conception of this study was motivated by the preliminary data showing that levels of blood protein and RNA transcripts related to interferon inflammation were predictive of future declines in lung function using Cox proportional hazards modeling.
An important feature of the study design is the focus on clinically relevant outcomes and clinical variables so that results can be immediately translated into clinical practice. This goal is realized in Aim 1, in which we will deliver the best performing clinical prediction model that relies only on clinically available data and lab tests to predict a clinical outcome used in pulmonary clinics to define sarcoidosis disease progression. This outcome is a clinically meaningful decline in lung function.
In Aim 2, we will measure the added value of incorporating novel blood-based interferon-related markers into the clinical prediction models. The goal of this aim is to identify which novel markers should be developed and moved into the clinical arena for use in sarcoidosis prognostication.
Finally, in Aim 3, we will apply these models to an important clinical management problem in sarcoidosis, which is identifying the optimal monitoring frequency for a given patient. Addressing this last question is the first step towards being able to better anticipate disease progression before extensive organ damage occurs.
The team of sarcoidosis investigators are highly qualified to execute this study because they have a track record of performing sarcoidosis clinical research, have ongoing collaborations, and have participated in prior studies that involve biospecimen collection from patients, including NIH-sponsored consortium studies.
To execute this study, the investigators will contribute longitudinal biospecimens and clinical data from 357 patients with sarcoidosis that have been enrolled in longitudinal cohorts at centers across the US. Two hundred additional patients will be enrolled and followed for up to 39 months, leading to a total sample size of 557, of which a majority will be African American.
Our team also includes a uniquely qualified biostatistician, Dr. Charles McCulloch, who has pioneered aspects of the longitudinal modeling approach we will be using. Therefore, the proposed aims have a high likelihood of success for tackling this long-overdue clinical problem.
The purpose of this proposal is to develop clinical prediction tools to risk stratify patients with pulmonary sarcoidosis. Because the course of sarcoidal inflammation lasts for many years even in those with self-limiting sarcoid, the lack of prognostic indicators upon which to develop a management plan is not a trivial issue for both patient and physician.
Thus, without prognostication tools, clinicians will not be able to improve the longitudinal care they provide for the types of outcomes that are used in the clinic. The conception of this study was motivated by the preliminary data showing that levels of blood protein and RNA transcripts related to interferon inflammation were predictive of future declines in lung function using Cox proportional hazards modeling.
An important feature of the study design is the focus on clinically relevant outcomes and clinical variables so that results can be immediately translated into clinical practice. This goal is realized in Aim 1, in which we will deliver the best performing clinical prediction model that relies only on clinically available data and lab tests to predict a clinical outcome used in pulmonary clinics to define sarcoidosis disease progression. This outcome is a clinically meaningful decline in lung function.
In Aim 2, we will measure the added value of incorporating novel blood-based interferon-related markers into the clinical prediction models. The goal of this aim is to identify which novel markers should be developed and moved into the clinical arena for use in sarcoidosis prognostication.
Finally, in Aim 3, we will apply these models to an important clinical management problem in sarcoidosis, which is identifying the optimal monitoring frequency for a given patient. Addressing this last question is the first step towards being able to better anticipate disease progression before extensive organ damage occurs.
The team of sarcoidosis investigators are highly qualified to execute this study because they have a track record of performing sarcoidosis clinical research, have ongoing collaborations, and have participated in prior studies that involve biospecimen collection from patients, including NIH-sponsored consortium studies.
To execute this study, the investigators will contribute longitudinal biospecimens and clinical data from 357 patients with sarcoidosis that have been enrolled in longitudinal cohorts at centers across the US. Two hundred additional patients will be enrolled and followed for up to 39 months, leading to a total sample size of 557, of which a majority will be African American.
Our team also includes a uniquely qualified biostatistician, Dr. Charles McCulloch, who has pioneered aspects of the longitudinal modeling approach we will be using. Therefore, the proposed aims have a high likelihood of success for tackling this long-overdue clinical problem.
Funding Goals
THE DIVISION OF LUNG DISEASES SUPPORTS RESEARCH AND RESEARCH TRAINING ON THE CAUSES, DIAGNOSIS, PREVENTION, AND TREATMENT OF LUNG DISEASES AND SLEEP DISORDERS. RESEARCH IS FUNDED THROUGH INVESTIGATOR-INITIATED AND INSTITUTE-INITIATED GRANT PROGRAMS AND THROUGH CONTRACT PROGRAMS IN AREAS INCLUDING ASTHMA, BRONCHOPULMONARY DYSPLASIA, CHRONIC OBSTRUCTIVE PULMONARY DISEASE, CYSTIC FIBROSIS, RESPIRATORY NEUROBIOLOGY, SLEEP AND CIRCADIAN BIOLOGY, SLEEP-DISORDERED BREATHING, CRITICAL CARE AND ACUTE LUNG INJURY, DEVELOPMENTAL BIOLOGY AND PEDIATRIC PULMONARY DISEASES, IMMUNOLOGIC AND FIBROTIC PULMONARY DISEASE, RARE LUNG DISORDERS, PULMONARY VASCULAR DISEASE, AND PULMONARY COMPLICATIONS OF AIDS AND TUBERCULOSIS. THE DIVISION IS RESPONSIBLE FOR MONITORING THE LATEST RESEARCH DEVELOPMENTS IN THE EXTRAMURAL SCIENTIFIC COMMUNITY AS WELL AS IDENTIFYING RESEARCH GAPS AND NEEDS, OBTAINING ADVICE FROM EXPERTS IN THE FIELD, AND IMPLEMENTING PROGRAMS TO ADDRESS NEW OPPORTUNITIES. 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
San Francisco,
California
941432204
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 312% from $1,153,760 to $4,751,121.
San Francisco Regents Of The University Of California was awarded
Pulmonary Sarcoidosis Prediction Models Enhanced Clinical Management
Project Grant R01HL157533
worth $4,751,121
from National Heart Lung and Blood Institute in April 2022 with work to be completed primarily in San Francisco California United States.
The grant
has a duration of 4 years and
was awarded through assistance program 93.837 Cardiovascular Diseases Research.
The Project Grant was awarded through grant opportunity NIH Research Project Grant (Parent R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 8/20/25
Period of Performance
4/1/22
Start Date
3/31/26
End Date
Funding Split
$4.8M
Federal Obligation
$0.0
Non-Federal Obligation
$4.8M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R01HL157533
Transaction History
Modifications to R01HL157533
Additional Detail
Award ID FAIN
R01HL157533
SAI Number
R01HL157533-472531783
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
KMH5K9V7S518
Awardee CAGE
4B560
Performance District
CA-11
Senators
Dianne Feinstein
Alejandro Padilla
Alejandro Padilla
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) | $2,314,781 | 100% |
Modified: 8/20/25