This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.Does the body's immune system play a role in the development of problems involving the nervous system in people with diabetes?Diabetes is known to be connected with problems involving the eyes, kidneys and nervous system. Little is known about why people develop problems with their nervous system in diabetes. Patients with diabetes report:-Pain-Tingling-Numbness and loss of feeling in their feet and legs.An increased number of antibodies in the blood that can attach to nerve cells and injure the nerve cells have been reported in patients with diabetes. Antibodies are proteins made by your body. The antibodies protect you from infections. Sometimes our body will make antibodies that attach to our own tissues. This type of antibody injures the tissues. These antibodies are called autoantibodies. It is not known why or when these autoantibodies develop in diabetes. We don't know whether these antibodies contribute to the development of complications involving the nervous system. Our study is designed to help answer the following questions:1. When do antibodies begin to appear in people with diabetes? 2. Does the presence of antibodies increase over time?3. Do the antibodies attach to nerve cells?4. If these antibodies attach to nerve cells, what are they specifically attaching to?5. Do these antibodies injure nerve cells?6. If the antibodies cause injury to nerve cells, how does this happen?We hope that answering these questions will lead to better treatments for the nervous system problems associated with diabetes in the future. Type 2 Diabetes is the most common form of diabetes and it affects millions of Americans every year. We will examine the hypothesis that a significant percentage of patients with Type 2 Diabetes will slowly develop autoantibodies during the course of their illness and that these autoantibodies contribute to the injury and loss of cells in the nervous system, a well-known complication in long-term diabetic patients.A total of 120 people 18 years or older will be enrolled into this study. Two groups of people with Type 2 Diabetes and one group of healthy volunteers will be studied. Group 1 will include people with Type 2 Diabetes newly diagnosed and up to 2 years prior to their start in this study. Group 2 will include people with Type 2 Diabetes diagnosed 7 to 9 years prior to their start in this study, and Group 3 will include healthy volunteers. All groups will undergo a thorough examination of their nervous system function and have blood drawn to screen for the presence of autoantibodies. All participants will undergo re-evaluation between four to five years after the initial testing. These studies will help to determine the significance of autoimmune mechanisms in the natural history of nerve injury that occurs in Type 2 Diabetes Mellitus.'

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000042-47
Application #
7603776
Study Section
Special Emphasis Panel (ZRR1-CR-8 (02))
Project Start
2007-03-01
Project End
2007-09-16
Budget Start
2007-03-01
Budget End
2007-09-16
Support Year
47
Fiscal Year
2007
Total Cost
$16,495
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Robarge, Jason D; Desta, Zereunesay; Nguyen, Anne T et al. (2017) Effects of exemestane and letrozole therapy on plasma concentrations of estrogens in a randomized trial of postmenopausal women with breast cancer. Breast Cancer Res Treat 161:453-461
Crane, Natania A; Jenkins, Lisanne M; Bhaumik, Runa et al. (2017) Multidimensional prediction of treatment response to antidepressants with cognitive control and functional MRI. Brain 140:472-486
Hertz, Daniel L; Speth, Kelly A; Kidwell, Kelley M et al. (2017) Variable aromatase inhibitor plasma concentrations do not correlate with circulating estrogen concentrations in post-menopausal breast cancer patients. Breast Cancer Res Treat 165:659-668
Hertz, D L; Kidwell, K M; Seewald, N J et al. (2017) Polymorphisms in drug-metabolizing enzymes and steady-state exemestane concentration in postmenopausal patients with breast cancer. Pharmacogenomics J 17:521-527
Kadakia, Kunal C; Kidwell, Kelley M; Seewald, Nicholas J et al. (2017) Prospective assessment of patient-reported outcomes and estradiol and drug concentrations in patients experiencing toxicity from adjuvant aromatase inhibitors. Breast Cancer Res Treat 164:411-419
Spengler, Erin K; Kleiner, David E; Fontana, Robert J (2017) Vemurafenib-induced granulomatous hepatitis. Hepatology 65:745-748
Heidemann, Lauren; Law, James; Fontana, Robert J (2017) A Text Searching Tool to Identify Patients with Idiosyncratic Drug-Induced Liver Injury. Dig Dis Sci 62:615-625
Law, Ian H; Alam, Osman; Bove, Edward L et al. (2016) Follow-Up of a Prospective Surgical Strategy to Prevent Intra-Atrial Reentrant Tachycardia After the Fontan Operation. Circ Arrhythm Electrophysiol 9:
Schrepf, Andrew; Harper, Daniel E; Harte, Steven E et al. (2016) Endogenous opioidergic dysregulation of pain in fibromyalgia: a PET and fMRI study. Pain 157:2217-2225
As-Sanie, Sawsan; Kim, Jieun; Schmidt-Wilcke, Tobias et al. (2016) Functional Connectivity is Associated With Altered Brain Chemistry in Women With Endometriosis-Associated Chronic Pelvic Pain. J Pain 17:1-13

Showing the most recent 10 out of 1380 publications