[PPI: new strategies for GERD]

Nihon Rinsho. 2004 Aug;62(8):1570-6.
[Article in Japanese]

Abstract

Proton pump inhibitor (PPI) is the first-line drug for GERD and is far more effective than H2-receptor antagonist (H2RA). H2RA suppresses mainly nocturnal gastric acid secretion from parietal cells, while PPI blocks acid production at nighttime as well as daytime when acid refluxes often occur. PPI-test is a therapeutic diagnosis and can reliably distinguish GERD from other diseases presenting similar symptoms. Initial therapy of GERD should be started with a full dose of PPI. However, most of the GERD patients need maintenance therapy. The maintenance dose of PPI should be individualized with a titration technique ('New Step-down therapy'). A small number of GERD patients resistant to PPI therapy may be due to nocturnal acid breakthrough (NAB) or rapid metabolism of PPI (extensive metabolizer for CYP2C19).

Publication types

  • Review

MeSH terms

  • 2-Pyridinylmethylsulfinylbenzimidazoles
  • Antacids
  • Aryl Hydrocarbon Hydroxylases / physiology
  • Benzimidazoles
  • Circadian Rhythm
  • Cytochrome P-450 CYP2C19
  • Depression, Chemical
  • Drug Resistance
  • Enzyme Inhibitors / administration & dosage*
  • Enzyme Inhibitors / metabolism
  • Enzyme Inhibitors / pharmacology
  • Gastric Acid / metabolism
  • Gastroesophageal Reflux / drug therapy*
  • Histamine H2 Antagonists / pharmacology
  • Histamine H2 Antagonists / therapeutic use
  • Humans
  • Lansoprazole
  • Mixed Function Oxygenases / physiology
  • Omeprazole / analogs & derivatives*
  • Proton Pump Inhibitors*
  • Rabeprazole

Substances

  • 2-Pyridinylmethylsulfinylbenzimidazoles
  • Antacids
  • Benzimidazoles
  • Enzyme Inhibitors
  • Histamine H2 Antagonists
  • Proton Pump Inhibitors
  • Lansoprazole
  • Rabeprazole
  • Mixed Function Oxygenases
  • Aryl Hydrocarbon Hydroxylases
  • CYP2C19 protein, human
  • Cytochrome P-450 CYP2C19
  • Omeprazole