Translations:Diabetes medication/54/en: Difference between revisions

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Message definition (Diabetes medication)
|-
| [[Metformin]]
| Acts on the liver to reduce gluconeogenesis and causes a decrease in [[insulin resistance]] via increasing [[AMPK]] signalling.
|
* Associated with weight loss
* Lower risk of hypoglycemia compared to other antidiabetics
* Decreases [[low-density lipoprotein]]
* Decreases [[triglycerides]]
* No effect on blood pressure
* Lowered all-cause mortality in diabetics
* Inexpensive
|
* Higher risk of [[Human gastrointestinal tract|gastrointestinal]] side effects
* Due to the risk of potentially fatal [[lactic acidosis]], contraindicated in people with [[shock (circulatory)|shock]]; with acute or chronic, moderate or severe [[kidney disease]] or at risk for impaired kidney function from [[Radiocontrast agent|intravenous dye]]; and with acute or chronic [[metabolic acidosis]]
* Risk of lactic acidosis also is increased for people with unstable or acute [[heart failure]], [[liver disease]], or [[alcoholism]], or who are recovering from major [[surgery]]
* Increased risk of [[vitamin B12 deficiency]]
* [[Metallic taste]]
|-
| [[Alpha-glucosidase inhibitor]]s ([[acarbose]], [[miglitol]], [[voglibose]])
| Inhibit carbohydrate digestion in the small intestine by inhibiting enzymes that break down polysaccharides
|
* Slightly lower risk of hypoglycemia compared to sulfonylureas
* Associated with modest weight loss
* Decreases triglycerides
* No detrimental effect on cholesterol
|
* Less effective than most other diabetes pills in lowering [[glycated hemoglobin]]
* Increased risk of GI side effects than other diabetes pills except metformin
* Inconvenient dosing
|-
| [[Thiazolidinediones]] ([[Pioglitazone]], [[Rosiglitazone]])
| Reduce insulin resistance by activating [[Peroxisome proliferator-activated receptor gamma|PPAR-γ]] in fat and muscle
|
* Lower the risk of hypoglycemia
* May slightly increase [[high-density lipoprotein]]
* Rosiglitazone linked to decreased triglycerides
* Convenient dosing
|
* Increase the risk of [[heart failure]]
* Cause an average of 2–5 kg [[weight gain]]
* Are associated with a higher risk of edema, anemia and bone fractures
* Can increase low-density lipoprotein
* Rosiglitazone has been linked to increased triglycerides and an increased risk of a heart attack
* Pioglitazone has been linked to an increased risk of bladder cancer
* Have a slower onset of action
* Require monitoring for [[hepatotoxicity]]
* Expensive
|-
|[[SGLT2 inhibitors]]
|}

|- | Metformin | Acts on the liver to reduce gluconeogenesis and causes a decrease in insulin resistance via increasing AMPK signalling. |

  • Associated with weight loss
  • Lower risk of hypoglycemia compared to other antidiabetics
  • Decreases low-density lipoprotein
  • Decreases triglycerides
  • No effect on blood pressure
  • Lowered all-cause mortality in diabetics
  • Inexpensive

|

|- | Alpha-glucosidase inhibitors (acarbose, miglitol, voglibose) | Inhibit carbohydrate digestion in the small intestine by inhibiting enzymes that break down polysaccharides |

  • Slightly lower risk of hypoglycemia compared to sulfonylureas
  • Associated with modest weight loss
  • Decreases triglycerides
  • No detrimental effect on cholesterol

|

  • Less effective than most other diabetes pills in lowering glycated hemoglobin
  • Increased risk of GI side effects than other diabetes pills except metformin
  • Inconvenient dosing

|- | Thiazolidinediones (Pioglitazone, Rosiglitazone) | Reduce insulin resistance by activating PPAR-γ in fat and muscle |

  • Lower the risk of hypoglycemia
  • May slightly increase high-density lipoprotein
  • Rosiglitazone linked to decreased triglycerides
  • Convenient dosing

|

  • Increase the risk of heart failure
  • Cause an average of 2–5 kg weight gain
  • Are associated with a higher risk of edema, anemia and bone fractures
  • Can increase low-density lipoprotein
  • Rosiglitazone has been linked to increased triglycerides and an increased risk of a heart attack
  • Pioglitazone has been linked to an increased risk of bladder cancer
  • Have a slower onset of action
  • Require monitoring for hepatotoxicity
  • Expensive

|- |SGLT2 inhibitors |}