Presentation notes on Diabetes Mellitus Classifications, Types, Insulin Deficiency & Drugs for Medical & Biology Students in PPT / word / .doc Format
CLASSIFICATION OF DIABETES MELLITUS
Although all forms of diabetes mellitus share hyperglycemia
as a common feature, the pathogenic processes involved in the development of
hyperglycemia vary widely. The previous classification schemes of diabetes
mellitus were based on the age at onset of the disease or on the mode of
therapy ; in contrast, the recently revised classification reflects our greater
understanding of the pathogenesis of each variant. The vast majority of cases
of diabetes fall into one of two broad classes :
Type 1 : Diabetes
is characterized by an absolute deficiency of insulin
caused by pancreatic b cell
destruction. It accounts for approximately 10% of all cases.
Type 2 : Diabetes
is caused by a combination of peripheral resistance to insulin action and
inadequate secretory response by the pancreatic b cells.
Approximately 80% to 90% of patients have type 2 diabetes.
A variety of monogenic and secondary causes are responsible
for the remaining cases. It should be stressed that while the major types of
diabetes have different pathogenic mechanisms, the long – term complications in
kidneys, eyes, nerves, and blood vessels are the same, as are the principal
causes of morbidity and death. The pathogenesis of the two major types is
discussed separately.
1. Type 1diabetes (b cell
destruction, leads to absolute insulin deficiency)
- Immune mediated
- Idiopathic
2. Type 2 diabetes (insulin resistance with relative insulin
deficiency).
3. Genetic defects of b cell
function.
- Maturity onset diabetes of the young (MODY),
caused by mutations in :
-
Hepatocyte nuclear factor 4a (HNF –
4a) (MODY3).
-
Glucokinase (MODY2).
-
Hepatocyte nuclear factor 1a (HNF -
1a) (MODY5).
-
Insulin promoter factor 1b (HNF -
1b) (MODY5).
-
Hepatocyte nuclear factor 1b (HNF-
1b) (MODY5)
-
Neurogenic differentiation factor 1 (Neuro D1)
(MODY6).
- Mitochondrial DNA mutations.
4. Genetic defects in insulin processing or insulin action
- Defects in proinsulin conversion.
- Insulin gene mutations.
- Insulin receptor mutations.
5. Exocrine pancreatic defects.
- Chronic pancreatitis
- Pancreatectomy
- Neoplasia
- Cystic fibrosis
- Hemachromatosis
- Fibrocalculous pancreatopathy.
6. Endocrinopathies
- Acromegaly
- Cushing syndrome
- Hyperthyroidism
- Pheochromocytoma
- Glucagonoma.
7. Infections
- Cytomegalovirus
- Coxackie virus B.
8. Drugs
- Glucocorticoids
- Thyroid hormone
- a -
interferon
- Protease inhibitors
- b -
adrenergic agonists
- Thiazides
- Nicotinic acid
- Phenytoin.
9. Genetic syndromes associated with diabetes
- Down syndrome
- Kleinfelter syndrome
- Turner syndrome.
10.Gestational diabetes mellitus
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