Work done in part by researchers at The University of Texas Health Science Center at Houston has led to the discovery of two new genes2 that are implicated3 in ankylosing spondylitis关节固定性脊柱炎 (AS), an inflammatory炎症的 and potentially disabling disease. In addition, the international research team pinpointed4 two areas along stretches of DNA5 that play an important role in regulating gene1 activity associated with the arthritic6关节炎的 condition. The findings, a critical milestone7 in the understanding of AS, are published in the January issue of Nature Genetics, a journal that emphasizes research on the genetic8 basis for common and complex diseases. "This helps us better understand what is driving this disease and gives us direction for new treatments and diagnostic tests," said John D. Reveille, M.D., the study's principal investigator9 and professor and director of the Division of Rheumatology and Clinical Immunogenetics at The University of Texas Medical School at Houston.
Reveille, the university's Linda and Ronny Finger Foundation Distinguished著名的 Chair in Neuroimmunologic Disorders11, and Matthew A. Brown, M.D., professor of immunogenetics免疫遗传学 at Australia's University of Queensland, led the research by the Triple "A" Spondylitis Consortium Genetic Study (i.e. the TASC or Australo-Anglo-American Spondylitis Consortium). Based on work from a genome-wide association scan, the team identified genes ANTXR2 and IL1R2 as well as two gene deserts, segments of DNA between genes on chromosomes染色体 2 and 21 that are associated with ankylosing spondylitis. Importantly, the study also confirmed the Triple "A" Australo-Anglo-American Spondylitis Consortium's previously13 reported associations of genes IL23R and ERAP1, formerly14 known as ARTS1.
Reveille, chief of rheumatology风湿病学 at Memorial Hermann-Texas Medical Center, said the genetic discoveries bring the scientific community closer to fully15 understanding AS, a chronic16 form of arthritis17 that attacks the spine18 and also can target other joints19 and organs in the body. The Centers for Disease Control and Prevention for the National Arthritis Data Workgroup estimates that AS and its related diseases affect as many as 2.4 million people in the United States. It generally strikes patients in their teens, 20s or 30s and can cause a complete fusion20 of the spine, leaving patients unable to straighten and bend.
Steve Haskew, who has lived with AS for more than three decades, said these genetic discoveries offer hope to patients, especially those newly diagnosed.
"When I first started experiencing lower back pain and the aching joints, no one could tell me what was wrong," said Haskew, co-leader of an AS support group. "It's fascinating to see how far we've come and how much has been learned about the disease."
Laurie Savage21, co-principal investigator and executive director of the Spondylitis Association of America (SAA) said, "These new breakthroughs are, indeed, good news for those whom we serve. It is very encouraging to know that the health impact and economic consequences of spondyloarthritis in the world eventually will be contained as a direct consequence of the dedication22 of Drs. Reveille, Brown and colleagues, and that of the many individuals affected23 by spondyloarthritis who have participated in these studies."