Genetic and morphologic determinants of pneumothorax in lymphangioleiomyomatosis

1 Pulmonary Critical Care Medicine Branch, 2 Warren G. Magnuson Clinical Center, Diagnostic Radiology Department, and 3 Office of Biostatistics Research, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland Submitted 1 May 2007 ; accepted in final form 29 June 2007 Lymphangioleiomyomatosis, a multisystem disease affecting women, is characterized by proliferation of abnormal smooth muscle-like cells in the lungs, leading to cystic destruction of the parenchyma and recurrent pneumothoraces. Clinical characteristics of lymphangioleiomyomatosis patients were analyzed to determine the relationship of pneumothoraces to disease progression. Patients were genotyped for polymorphisms in genes of extracellular matrix proteins collagen, elastin, and matrix metalloproteinase-1 to assess their association with pneumothoraces. Clinical data and polymorphisms in the genes for types I and III collagen, elastin, and matrix metalloproteinase-1 were compared with the prevalence of pneumothorax. Of 227 patients, 57% reported having had at least one pneumothorax. Cyst size on high-resolution computed tomography scans was associated with pneumothorax; patients with a history of pneumothorax were more likely to have larger cysts than patients who had no pneumothoraces. In patients with mild disease, those with a history of pneumothorax had a faster rate of decline in forced expiratory volume in 1 s (FEV 1 ; P = 0.001, adjusted for age) than those without. Genotype frequencies differed between patients with and without pneumothorax for polymorphisms in the types I and III collagen and matrix metalloproteinase-1 genes. Larger cysts may predispose lymphangioleiomyomatosis patients to pneumothorax, which, in early stages of disease, correlates with a more rapid rate of decline in FEV 1 . Polymorphisms in types I and III collagen and matrix metalloproteinase-1 genes may cause differences in lung extracellular matrix that result in greater susceptibility to pneumothorax. cystic lung disease; collagen; matrix metalloproteinases; elastin Address for reprint requests and other correspondence: J. Moss, Pulmonary Critical Care Medicine Branch, National Institutes of Health, National Heart, Lung, and Blood Institute, Bldg. 10, Rm. 6D03, MSC 1590, Bethesda, MD 20892-1590 (e-mail: mossj{at}nhlbi.nih.gov )