(PHILADELPHIA) -- Researchers are advancing against a rare, deadly lung disease (related to hormones) that no one had even heard of a decade ago. The disease targets only women, striking them down during their childbearing years. It can be triggered by pregnancy, progresses rapidly, and often results in death within ten years.
Vera Krymskaya, PhD, Research Associate Professor of Medicine in the Pulmonary, Allergy and Critical Care Division at the University of Pennsylvania School of Medicine, has dedicated the last several years of her career to combating Lymphangioleimyomatosis (LAM). The disease causes extensive, abnormal smooth muscle-like cell proliferation, which invades and destroys the tissues of the lung by forming cysts, eventually obstructing the flow of air and leading to lung collapse and failure.
Solving the puzzle…
Globally, researchers tackled the first step, finding out what caused the cell proliferation and identifying the mutating gene that was responsible. Next, Krymskaya’s lab at the University of Pennsylvania was responsible for the breakthrough step of discovering the function of the gene that caused the cell malfunction, paving the way for a potential treatment utilizing a medication to inhibit abnormal growth. This treatment is now in a clinical trial.
As many as 250,000 women may be suffering from LAM, but many are misdiagnosed with asthma or emphysema or remain undiagnosed. Krymskaya explains "the key to combating this disease is to educate physicians to know how to diagnose LAM and treat it in its earliest stages before the damage to the lung is done and a transplant is needed. A biopsy and a high resolution CT scan, not just an X-ray, are needed to detect LAM."Sue Byrnes - who founded The LAM Foundation, an international non-profit organization focused on research, after her daughter was diagnosed with LAM, adds, "This heart wrenching disease strikes women as they are beginning their careers, getting married and starting families, just when their futures look so bright. Women with LAM often struggle to breathe. They experience lung collapses, chest pain, cough, and can become extremely fatigued. Many of them develop a benign kidney tumor. Supplemental oxygen is inevitable, and a lung transplant, which usually buys them only a few years, is the very last resort for survival."
One woman’s struggle…
43-year-old Sheila Egan Addis, a Philadelphia theatrical performer and mother of two, who lives in Center City, started suffering from alternating collapsed lungs when she turned 30. "It felt like a sharp pain in my upper back, like I’d pulled a muscle when I tried to take a deep breath," Egan Addis comments. After the third time each lung had collapsed, surgeons went in to restore some of the lung function. Nine years after she began suffering symptoms, a Penn pulmonologist finally diagnosed her with LAM disease. "Finally, it all made sense," Egan Addis adds.
Two years ago, her right lung collapsed again and she was operated on. Egan Addis has since lost some more lung function. She says it does take a toll on a performer in live musical theater, "I don't have the stamina that I used to. I can't do a lot of running around and singing. I have to think about it before taking on a challenging role. The pace of live theater can be very tiring and draining physically."
There is hope…
Krymskaya’s discovery in 2002 revealed that abnormal smooth muscle-like LAM cells invading the lungs are due to the loss of growth control by tuberous sclerosis (a genetic disorder which causes tumors to form in organs) complex proteins - and furthermore, Krymskaya then discovered that growth can potentially be controlled by a drug (FDA-approved Rapamycin), which mimics the function of the missing proteins. Krymskaya made the link between similar basic research found in flies and applied it to humans, opening the door for the first-ever LAM treatment clinical trial now underway.
Globally, researchers are excited about discovering more about LAM because of the close relationship between it and other diseases. "If we solve this puzzle, it may very well lead to answers regarding other deadly diseases like heart and vascular disease, cancer and diabetes," Krymskaya notes.
Funding for LAM research was provided through the LAM Foundation as well as various grants from the National Institutes of Health.
For more information on the Penn Lung Center, go on-line to: http://pennhealth.com/lung/services/pvd.html
Vera Krymskaya, PhD -- on-line bio: http://www.uphs.upenn.edu/lungctr/paccd/pulmonary/physicians_staff/faculty/krymska.html
Image of normal lung tissue versus LAM lung tissue available upon request. Please include: Courtesy: Vera Krymskaya, PhD, University of Pennsylvania School of Medicine.
Photo of Dr. Krymskaya available upon request.
For more information on the LAM Foundation, visit: www.thelamfoundation.org
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Last reviewed: By John M. Grohol, Psy.D. on 21 Feb 2009
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