Exposure to beryllium dust causes a chronic lung disease, chronic beryllium disease (CBD), in some people. It may also cause beryllium sensitization, a reaction similar to an allergy. This sensitivity precedes the development of CBD. Once a person becomes sensitized to beryllium, he or she has cells in the blood or lungs capable of reacting to beryllium. These cells are the cause of the lung inflammation in CBD. The goals of the study Immunopathogenesis of Beryllium Disease are to better understand the ways in which cells of the immune system react to beryllium and to develop tests to measure beryllium allergy. Some individuals may have a genetic (inborn) susceptibility to develop beryllium sensitization. Studies have identified a genetic marker located on white blood cells, which is associated with chronic beryllium disease. The studies have not yet determined whether this marker alone identifies who will develop the disease. Our study is designed to try to determine what genetic markers control the allergic reaction to beryllium. Using a group of white blood cells called T-lymphocytes from the blood and lung, we are studying the relationship between the immune system response in CBD and a person's genetic make-up. Participation involves completion of a questionnaire regarding medical symptoms and work history; blood for immunologic and genetic laboratory studies; pulmonary function testing, exercise physiology testing and chest x-rays to determine disease progression; and bronchoalveolar lavage to determine disease progression and to obtain cells for immunologic and genetic laboratory studies. Participants are followed on an annual or biannual basis, depending on the severity of their disease.

Project Start
1999-12-01
Project End
2000-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
39
Fiscal Year
2000
Total Cost
$32,212
Indirect Cost
Name
University of Colorado Denver
Department
Type
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Millstein, Richard J; Pyle, Laura L; Bergman, Bryan C et al. (2018) Sex-specific differences in insulin resistance in type 1 diabetes: The CACTI cohort. J Diabetes Complications 32:418-423
Martin, Maureen P; Naranbhai, Vivek; Shea, Patrick R et al. (2018) Killer cell immunoglobulin-like receptor 3DL1 variation modifies HLA-B*57 protection against HIV-1. J Clin Invest 128:1903-1912
Nowak, Kristen L; You, Zhiying; Gitomer, Berenice et al. (2018) Overweight and Obesity Are Predictors of Progression in Early Autosomal Dominant Polycystic Kidney Disease. J Am Soc Nephrol 29:571-578
Haas, David W; Bradford, Yuki; Verma, Anurag et al. (2018) Brain neurotransmitter transporter/receptor genomics and efavirenz central nervous system adverse events. Pharmacogenet Genomics 28:179-187
Venuto, Charles S; Lim, Jihoon; Messing, Susan et al. (2018) Inflammation investigated as a source of pharmacokinetic variability of atazanavir in AIDS Clinical Trials Group protocol A5224s. Antivir Ther 23:345-351
Li, Binglan; Verma, Shefali S; Veturi, Yogasudha C et al. (2018) Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression. Pac Symp Biocomput 23:448-459
Hayden, Kathleen M; Baker, Laura D; Bray, George et al. (2018) Long-term impact of intensive lifestyle intervention on cognitive function assessed with the National Institutes of Health Toolbox: The Look AHEAD study. Alzheimers Dement (Amst) 10:41-48
Shah, V N; Sippl, R; Joshee, P et al. (2018) Trabecular bone quality is lower in adults with type 1 diabetes and is negatively associated with insulin resistance. Osteoporos Int 29:733-739
Jensen, Thomas; Bjornstad, Petter; Johnson, Richard J et al. (2018) Copeptin and Estimated Insulin Sensitivity in Adults With and Without Type 1 Diabetes: The CACTI Study. Can J Diabetes :
Dad, Taimur; Abebe, Kaleab Z; Bae, K Ty et al. (2018) Longitudinal Assessment of Left Ventricular Mass in Autosomal Dominant Polycystic Kidney Disease. Kidney Int Rep 3:619-624

Showing the most recent 10 out of 1065 publications