Skip to main content
Thorax logoLink to Thorax
. 2000 Feb;55(2):143–146. doi: 10.1136/thorax.55.2.143

Adult familial cryptogenic fibrosing alveolitis in the United Kingdom

R Marshall 1, A Puddicombe 1, W Cookson 1, G Laurent 1
PMCID: PMC1745672  PMID: 10639533

Abstract

BACKGROUND—Familial cases of cryptogenic fibrosing alveolitis (CFA) have previously been reported; however, the prevalence and genetic background of this disorder are not known. The clinical and epidemiological findings of 25 families identified within the UK are reported.
METHODS—Adult pulmonary physicians in the UK were asked to identify all families under their care in which two or more individuals had been diagnosed with fibrosing alveolitis of unknown cause. A detailed structured questionnaire was sent to each proband to delineate possible environmental/occupational exposures and to obtain complete pedigree data. Physicians were also asked to provide clinical and diagnostic information.
RESULTS—Twenty five families were identified comprising 67 cases. Suitable data for analysis were available for 21 families (57 cases). The male:female ratio was 1.75:1 (p<0.05). A high resolution computed tomographic (HRCT) scan was performed in 93% and a diagnosis of CFA confirmed on biopsy specimens in 32%. The mean age at diagnosis was 55.5 (2.5) years. Fifty percent of cases were ever smokers and 18% had been diagnosed as asthmatic. Exposure to known fibrogenic agents was recorded by 36% of patients. Clinical signs/symptoms and histological findings were indistinguishable from non-familial cases.
CONCLUSIONS—This study represents the largest cohort of familial CFA cases reported to date and confirms a prevalence of 1.34 cases per 106 in the UK population. Although rare, such cases represent an important subgroup in which a genetic susceptibility to pulmonary fibrosis is particularly evident. Familial patients are younger at diagnosis but otherwise indistinguishable from non-familial cases. The mode of inheritance is as yet unclear but a number of genetic loci are likely to be involved and are the subject of ongoing studies.



Full Text

The Full Text of this article is available as a PDF (66.1 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Auwerx J., Demedts M., Bouillon R., Desmet J. Coexistence of hypocalciuric hypercalcaemia and interstitial lung disease in a family: a cross-sectional study. Eur J Clin Invest. 1985 Feb;15(1):6–14. doi: 10.1111/j.1365-2362.1985.tb00136.x. [DOI] [PubMed] [Google Scholar]
  2. Bitterman P. B., Rennard S. I., Keogh B. A., Wewers M. D., Adelberg S., Crystal R. G. Familial idiopathic pulmonary fibrosis. Evidence of lung inflammation in unaffected family members. N Engl J Med. 1986 May 22;314(21):1343–1347. doi: 10.1056/NEJM198605223142103. [DOI] [PubMed] [Google Scholar]
  3. Briggs D. C., Vaughan R. W., Welsh K. I., Myers A., duBois R. M., Black C. M. Immunogenetic prediction of pulmonary fibrosis in systemic sclerosis. Lancet. 1991 Sep 14;338(8768):661–662. doi: 10.1016/0140-6736(91)91235-m. [DOI] [PubMed] [Google Scholar]
  4. DONOHUE W. L., LASKI B., UCHIDA I., MUNN J. D. Familial fibrocystic pulmonary dysplasia and its relation to Hamman-Rich syndrome. Pediatrics. 1959 Nov;24:786–813. [PubMed] [Google Scholar]
  5. HERMANSKY F., PUDLAK P. Albinism associated with hemorrhagic diathesis and unusual pigmented reticular cells in the bone marrow: report of two cases with histochemical studies. Blood. 1959 Feb;14(2):162–169. [PubMed] [Google Scholar]
  6. Hubbard R., Lewis S., Richards K., Johnston I., Britton J. Occupational exposure to metal or wood dust and aetiology of cryptogenic fibrosing alveolitis. Lancet. 1996 Feb 3;347(8997):284–289. doi: 10.1016/s0140-6736(96)90465-1. [DOI] [PubMed] [Google Scholar]
  7. Johnston I. D., Prescott R. J., Chalmers J. C., Rudd R. M. British Thoracic Society study of cryptogenic fibrosing alveolitis: current presentation and initial management. Fibrosing Alveolitis Subcommittee of the Research Committee of the British Thoracic Society. Thorax. 1997 Jan;52(1):38–44. doi: 10.1136/thx.52.1.38. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Johnston I., Britton J., Kinnear W., Logan R. Rising mortality from cryptogenic fibrosing alveolitis. BMJ. 1990 Nov 3;301(6759):1017–1021. doi: 10.1136/bmj.301.6759.1017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Marshall R. P., McAnulty R. J., Laurent G. J. The pathogenesis of pulmonary fibrosis: is there a fibrosis gene? Int J Biochem Cell Biol. 1997 Jan;29(1):107–120. doi: 10.1016/s1357-2725(96)00141-0. [DOI] [PubMed] [Google Scholar]
  10. PEABODY J. W., PEABODY J. W., Jr, HAYES E. W., HAYES E. W., Jr Idiopathic pulmonary fibrosis; its occurrence in identical twin sisters. Dis Chest. 1950 Oct;18(4):330–344. doi: 10.1016/s0096-0217(15)34710-5. [DOI] [PubMed] [Google Scholar]
  11. Schrier D. J., Kunkel R. G., Phan S. H. The role of strain variation in murine bleomycin-induced pulmonary fibrosis. Am Rev Respir Dis. 1983 Jan;127(1):63–66. doi: 10.1164/arrd.1983.127.1.63. [DOI] [PubMed] [Google Scholar]
  12. Swaye P., Van Ordstrand H. S., McCormack L. J., Wolpaw S. E. Familial Hamman-Rich syndrome. Report of eight cases. Dis Chest. 1969 Jan;55(1):7–12. doi: 10.1378/chest.55.1.7. [DOI] [PubMed] [Google Scholar]
  13. Tal A., Maor E., Bar-Ziv J., Gorodischer R. Fatal desquamative interstitial pneumonia in three infants siblings. J Pediatr. 1984 Jun;104(6):873–876. doi: 10.1016/s0022-3476(84)80484-9. [DOI] [PubMed] [Google Scholar]
  14. Tisdale J. E., Follin S. L., Ordelova A., Webb C. R. Risk factors for the development of specific noncardiovascular adverse effects associated with amiodarone. J Clin Pharmacol. 1995 Apr;35(4):351–356. doi: 10.1002/j.1552-4604.1995.tb04072.x. [DOI] [PubMed] [Google Scholar]

Articles from Thorax are provided here courtesy of BMJ Publishing Group

RESOURCES