Effect of Iron Reduction by Phlebotomy for Type 2 Diabetes
Type 2 Diabetes Mellitus, Prediabetes

About this trial
This is an interventional treatment trial for Type 2 Diabetes Mellitus focused on measuring iron, diabetes, phlebotomy
Eligibility Criteria
Inclusion Criteria:
- Age 35-65
- Prediabetes, or diabetes relatively well-controlled (Hemoglobin A1c [HbA1c] ≤ 8.0%) with a single oral agent as defined by oral glucose tolerance testing (OGTT) using criteria of the American Diabetes Association.
- Serum ferritin values in the upper 50% of the normal range, 110-400 ng/mL for males, or 80-240 for females.
Exclusion Criteria:
- hereditary hemochromatosis;
- cancer (except cases currently with no evidence of disease);
- serum creatinine >1.5;
- anemia (Hgb < lower limit of normal);
- chronic inflammatory conditions (rheumatologic conditions such as rheumatoid arthritis or giant cell arteritis, or chronic infections such as hepatitis B or C) that could affect ferritin;
- erythrocyte sedimentation rate or C-reactive protein>1.5 times the upper limit of normal (UNL);
- serum transaminases 2 x UNL;
- hemophilia,
- warfarin therapy,
- history of GI bleeding;
- current glucocorticoid therapy.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Phlebotomy
Control
All subjects receive counseling to follow a healthy diet and regular exercise. Phlebotomy occurs at the rate of 500 ml (one Unit) of blood per month over the period of 3-6 months. At two-month intervals, serum ferritin and complete blood counts are determined. When serum ferritin reaches the lowest quartile of normal (<50 ng/mL for females and <70 ng/mL for males, but no sooner than 3 months or later than 6 months after beginning phlebotomy, subjects will be retested for glucose tolerance as described
Subjects receive counseling to follow a healthy diet and regular exercise.