The overall goal of this project is to investigate inherited genetic factors that play a role in the development of pulmonary fibrosis. The overall hypothesis of this investigation is that inherited genetic factors predispose individuals to develop pulmonary fibrosis. The goal of this investigation is to identify a group of genetic loci that play a role in the development of familial pulmonary fibrosis. The overall hypothesis is supported by the following observations: familial pulmonary fibrosis is indistinguishable pathologically from idiopathic pulmonary fibrosis and appears to be inherited as an autosomal dominant trait with variable penetrance; pulmonary fibrosis is associated with pleiotropic genetic disorders, such as Hermansky-Pudlak syndrome, neuofibromatosis, tuberous sclerosis, Neimann-Pick disease, Gaucher's disease, and familial hypocalciuric hypercalcemia; pulmonary fibrosis is frequently observed in autoimmune disease, including rheumatoid arthritis and systemic sclerosis; variable susceptibility is evident among workers who are reported to be exposed occupationally to similar concentrations of fibrogenic dusts; and inbred strains of mice differ in their susceptibility to fibrogenic dust. In conjunction with the exponential growth of human molecular genetics, the investigators state that these clinical observations suggest that a well organized approach to define the genetic determinants of pulmonary fibrosis is scientifically feasible and justified. This project proposes to use standard genetic methodology (linkage analysis) to investigate the distribution of polymorphisms for anonymous genetic markers in families with familial pulmonary fibrosis. The investigators state that their comprehensive genome-wide study, using standard genetic markers, will allow them to identify loci which subsequently may prove to contain novel genes that play a role in the pathogenesis of pulmonary fibrosis. Once genetic loci are defined in familial pulmonary fibrosis, candidate genes can be identified on the basis of both positional and functional criteria. Moreover, they note that this approach will provide basic information on high priority loci that will be applicable to the rapidly evolving dense human transcript map for pulmonary fibrosis in families with two or more cases of pulmonary fibrosis.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01HL067467-04
Application #
6637334
Study Section
Epidemiology and Disease Control Subcommittee 2 (EDC)
Program Officer
Reynolds, Herbert Y
Project Start
2000-08-20
Project End
2005-07-31
Budget Start
2003-08-01
Budget End
2004-07-31
Support Year
4
Fiscal Year
2003
Total Cost
$708,660
Indirect Cost
Name
Duke University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
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Seibold, Max A; Wise, Anastasia L; Speer, Marcy C et al. (2011) A common MUC5B promoter polymorphism and pulmonary fibrosis. N Engl J Med 364:1503-12
Brass, David M; Tomfohr, John; Yang, Ivana V et al. (2007) Using mouse genomics to understand idiopathic interstitial fibrosis. Proc Am Thorac Soc 4:92-100
Yang, Ivana V; Burch, Lauranell H; Steele, Mark P et al. (2007) Gene expression profiling of familial and sporadic interstitial pneumonia. Am J Respir Crit Care Med 175:45-54
Hollingsworth, John W; Whitehead, Gregory; Berman, Katherine Gray et al. (2007) Genetic basis of murine antibacterial defense to streptococcal lung infection. Immunogenetics 59:713-24
Hollingsworth, John W; Li, Zhuowei; Brass, David M et al. (2007) CD44 regulates macrophage recruitment to the lung in lipopolysaccharide-induced airway disease. Am J Respir Cell Mol Biol 37:248-53
Steele, Mark P; Speer, Marcy C; Loyd, James E et al. (2005) Clinical and pathologic features of familial interstitial pneumonia. Am J Respir Crit Care Med 172:1146-52
Savov, Jordan D; Whitehead, Gregory S; Wang, Jianme et al. (2004) Ozone-induced acute pulmonary injury in inbred mouse strains. Am J Respir Cell Mol Biol 31:69-77
Garantziotis, Stavros; Steele, Mark P; Schwartz, David A (2004) Pulmonary fibrosis: thinking outside of the lung. J Clin Invest 114:319-21
Savov, Jordan D; Brass, David M; Berman, Katherine G et al. (2003) Fibrinolysis in LPS-induced chronic airway disease. Am J Physiol Lung Cell Mol Physiol 285:L940-8

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