The Effect of Uric Acid Lowering in Type 1 Diabetes

Uric acid (UA) was recently suggested to exert deleterious effects on blood pressure and renal function, even when baseline UA levels are within the normal range. UA activates the renin angiotensin-aldosterone system (RAAS), increases oxidative stress and promotes inflammation. As a consequence, higher UA levels are associated with metabolic abnormalities (insulin resistance, hyperglycemia), cardiovascular disease (hypertension, endothelial dysfunction, arterial stiffness, cardiac diastolic dysfunction) and kidney function abnormalities (hyperfiltration - a marker for intraglomerular hypertension, proteinuria). Thus pharmacologic UA lowering may promote renal and cardiovascular protection. The mechanisms underlying these protective effects in humans, prior to the onset of clinical disease, remain unknown.

This study is focused on the prevention of complications in young, normotensive type 1 diabetes mellitus (T1DM) patients with normal renal function and UA levels. The study will examine the effect of UA lowering with febuxostat (FBX) on renal hemodynamic function, vascular function and urinary inflammatory biomarkers. Based on substantial supportive pre-clinical and epidemiological data, we hypothesize that lowering UA levels that are within normal range at baseline will: 1) ameliorate hemodynamic abnormalities characteristic of T1DM, and reduce renal and systemic hypertensive responses to hyperglycemia; 2) ameliorate endothelial function abnormalities characteristic of T1DM; 3) reduce urinary inflammatory cytokines/chemokine excretion.

Inclusion criteria

• Age 18-40 years old
• Normoalbuminuria 24 hour urine collection
• Body mass index 18-30 kg/m2 at screening
• Subject able, willing to perform assessments
• Normal electrocardiogram
• Normal renal (estimated GFR>60 ml/min)
• Clinic blood pressure <140/90 mmHg
• Type 1 DM, duration of diabetes >1 years
• Able to take medications every day
• Signed and dated written informed consent on the screening visit in accordance with GCP and local legislation
• Hemoglobin A1c 6-11%
• Normal uric acid levels

Exclusion criteria

• Cardiac, lung or peripheral vascular disease or stroke, gout
• Hypertension, or on BP-lowering medicine
• History of proliferative retinopathy
• Diagnosis of brittle diabetes based on investigator judgement
• Allergy to either allopurinol or probenecid
• Pregnancy, breastfeeding, no reliable contraception
• Oral contraceptives (due to effects on the RAS)
• Alcohol or tobacco within 24 hours prior to the study
• Uric acid ≥420 μmol/L or taking uric acid lowering agents
• Use of agents that influence GFR or interfere with purine metabolism (didanosine, azothioprine, methotrexate, NSAIDs, mycophenolate)
• Pancreas, pancreatic islet cells or renal transplant recipient
• Medical history of cancer or treatment for cancer in the last five years prior to screening
• T1DM treatment with any other drugs to reduce blood glucose except insulin within 6 months prior to screening (example: off-label use of metformin)
• Known autonomic neuropathy and proliferative retinopathy including treated proliferative retinopathy. Subjects with mild non-proliferative diabetic retinopathy can be included
• Alcohol or drug abuse within the three months prior to informed consent that would interfere with trial participation based on investigator judgement or any ongoing clinical condition that would jeopardize subject safety or study compliance based on investigator judgement
• ACE inhibitors, angiotensin receptor blockers, direct renin inhibitors, aldosterone antagonists
• Indication of liver disease, defined by serum levels of either alanine transaminase (ALT) (SGPT), aspartate transaminase (AST) (SGOT), or alkaline phosphatase above 3 x upper limit of normal (ULN) as determined during screening
• Blood disorders causing hemolysis or unstable red blood cells (e.g. malaria, hemolytic anemia)
• Pre-menopausal women (last menstruation ≤ 1 year prior to informed consent) who are nursing or pregnant or are of child-bearing potential and are not practising an acceptable method of birth control, or do not plan to continue using this method throughout the study.
• Participation in another trial with an investigational drug within 30 days prior to informed consent