WHO Definition of Diabetes Mellitus
A state of chronic hyperglycaemia which may result from genetic or environmental factors often acting jointly. Hyperglycaemia may be due to a lack of insulin or an excess of one or more factors that oppose the action of insulin.
Classification
Primary
- Type 1: Insulin dependent diabetes mellitus (IDDM) – severe, labile, occurs usually at younger age but can occur at any age, liable to develop ketoacidosis.
- Type 2: Non-insulin dependent diabetes mellitus (NIDDM) – not prone to ketoacidosis, patients are often obese, and is of maturity onset.
Secondary
1. Pancreatic disorders:
– Chronic pancreatitis
– Pancreatectomy/trauma
– Neoplasia
– Cystic fibrosis
– Hemachromatosis
– Fibrocalculous pancreatopathy
– Chronic pancreatitis
2. Endocrine disorders :
– Acromegaly
– Cushing syndrome
– Hyperthyroidism
– pheochromocytoma.
– glucagonoma.
3. Genetic disorders:
– hemochromatosis,
– syndrome X (metabolic syndrome),
– maturity onset diabetes of die young (MODY)
4. Drug induced:
– Glucocorticoids
– Thyroid hormone
– Interferon-α
– Protease inhibitors
– β-adrenergic agonists
– Thiazides
– Nicotinic acid
– Phenytoin (Dilantin)
5. Infections:
– Mumps
– Congenital rubella,
– Cytomegalovirus (AIDS patients)
Gestational
Glucose intolerance that develops during pregnancy.
Comparison between Type I and Type II Diabetes Mellitus
TYPE-1 TYPE-2
Age: < 40 Years >40years
Duration: Weeks Months To Years
Ketonuria: Common Rare
Insulin- Dependent Yes No
Autoantibody: Yes No
Family History: No Yes
Insulin Levels: Very Low Normal To High
Islets: Insulinitis Normal/Exaustion
Complications: Acute & Metabolic Late And Vascular
Ketoacidosis Microangiopathies