Description

The prospective observational study entitled "Heidelberg Study on Diabetes and Complications" is designed to show that diabetes according to the current medical definition does not exist. Without question, there is an autoimmune disease that destroys beta cells in the pancreas, which leads to absolute insulin deficiency with consecutively elevated blood glucose levels. This disease is defined as diabetes mellitus type 1. Insulin treatment is absolutely necessary in this state, since absolute insulin deficiency leads to lipolysis with consecutive ketoacidosis and eventually death. On the other hand, type 2 diabetes is generally defined as relative insulin deficiency with consecutively elevated blood glucose levels. This disease is often mentioned in the context of the metabolic syndrome, which additionally comprises obesity, arterial hypertension, dyslipidemia, and cardiovascular diseases. Therefore, only the name "diabetes mellitus" is shared by these two diseases, which means "sweet flow", therefore only describing a symptom.

Multiple interventional studies were aimed on avoiding or reducing the development of late diabetic complications (nephropathy, neuropathy, retinopathy, microangiopathy). This is true for both type 1 and type 2 diabetes. Up to this day, no study was able to demonstrate that treatment of normalization of blood glucose levels reduces or even reverses development of these complications. Moreover, several type 2 diabetic patients developed typical diabetic complications before definitive manifestation of the actual disease.

Therefore, we hypothesize that late diabetic complications stand in no primary context with blood glucose control, but are associated with other metabolic disorders. One aspect are reactive metabolites (glyoxal, methylglyoxal, 3-DG), which are formed in glycolysis and lipolysis in the context of energy production of cells. These metabolites are detoxified to lactate by certain enzymes. In case this detoxification is compromised, or production of these metabolites elevated, so called advanced glycation endproducts (AGEs) can form. Moreover, within the process of energy production, reactive oxygen species (ROS) and oxydative stress are more pronounced, which can have direct influence on cellular metabolism. This interaction leads to inflammation and DNA damage. Survival of the cells is dependent on defense mechanisms, which seem to be genetically determined, with cellular ageing playing a role as well (cellular senescence). With advanced ageing, cells lose these defense mechanisms against these permanent metabolic attacks.

Therefore, the following hypotheses arise:

1. Diabetes mellitus type 2 is no independent disease, but a late complication of metabolic imbalance
2. Typical "late diabetic complications" are not based on insufficient blood glucose lowering therapy, but on the basis of this metabolic imbalance, and can therefore affect every patient, even without manifested "diabetes mellitus type 2"
3. Diabetes mellitus type 1 is an autoimmundisease with consecutive absolute insulin deficiency, however manifestation of late diabetic complications is based on the same metabolic dysbalance (overlap with type 2).

In order to investigate these hypotheses, study participants will be profoundly examined once yearly concerning glycemic metabolic state and clinical findings related to micro- and macrovascular diabetic complications, Moreover, reactive metabolites like AGEs, ROS, methylglyoxal, and DNA damage as well as other parameters associated with cellular senescence will be examined. We will also collect information concerning quality of life, well-being, depression, and neuropathic pain.

This is the first study of its kind to include non-diabetics, pre-diabetics, and diabetics with the possibility to study differences and common ground regarding cellular metabolism. Moreover, to the best of our knowledge, there is no precise clinical characterization of peripheral nerve function in pre-diabetics, although some of these patients already complain about neuropathic symptoms. In addition to that, the natural clinical course not only in diabetics, but also in pre-diabetics will be observed over a longer period of time. Finally, changes in surrogate markers over the natural course of pre-diabetes can be observed for the first time, onset of type 1 or type 2 diabetes can be registered immediately, and all patients can be directly compared to healthy controls.

        1 or type 2 and diagnosis according to DDG guidelines 2011, that is HbA1c of 6,5 percent or
        higher after exclusion of false values, more than 200 mg per dl two hours after glucose in
        the oGTT, fasting glucose more than 126 mg per dl, spontaneous glucose more than 200 mg per
        dl at least twice Healthy persons without diabetes or impairment of glucose metabolism in
        the oGTT according to DDG guidelines 2011 fasting plasma glucose less than 100 mg per dl
        and 2 hour plasma glucose less than 140 mg per dl Pre diabetics with impaired fasting
        glucose between 100 mg per dl and 125 mg per dl, or impaired glucose tolerance with 2 hour
        glucose values between 140 and 199 mg per dl in the oGTT, all values from venous plasma
        Exclusion Criteria General exclusion criteria Secondary types of Diabetes, ADA criteria
        type 3 B H Current pregnancy Acute infections or fever Immune suppressant therapy Severe
        psychiatric diseases requiring treatment, including personality disorders, schizophrenia,
        depression Known alcohol or drug dependency Severe heart NYHA stadium IV, kidney, or liver
        insufficiency Non diabetic liver disease, for example PBC, PSC, Wilsons disease,
        hemochromatosis, autoimmune hepatitis severe peripheral artery disease stadium IV non
        diabetic glomerulopathy Cancer or other malignant diseases within the last 5 years
        Infectious diseases like hepatitis B, C, E, or HIV Other severe autoimmune diseases Current
        participation in an interventional study Anemia or disorders of bone marrow Exclusion
        criteria for MRI Pacemaker or ICD Metallic and magnetic implants, for example mechanic
        cardiac valves replacements, joint prostheses, clips after vascular surgery, middle or
        inner ear implants, recent tooth implants, penile implants Waist circumference more than
        135 cm Claustrophobia Allergies against MRI contrast Impaired kidney function with a GFR
        less than 65 ml per min
        Exclusion criteria for clamp study Past history of deep vein thrombosis or pulmonary
        embolism Routine laboratory test results less than 80 percent below lower reference value
        of Ferritin, iron, leucocytes, hemoglobin, hematocrite, RBC, platelets, blood alcohol Level
        Exclusion criteria for bioimpedance measurement Pacemaker or ICD
        Exclusion criteria for lung function testing Ignoring or non understanding of the
        instructions Body weight more than 160 kg