Metformin has traditionally been regarded as contraindicated in chronic kidney disease (CKD), though guidelines in recent years have been relaxed to permit therapy if the glomerular filtration rate (GFR) is > 30 mL/min. The main problem is the perceived risk of lactic acidosis (LA). Epidemiological evidence suggests that this fear is disproportionate. Lactic acidosis is a rare complication to type 2 diabetes mellitus (T2DM), with an incidence of 6/100,000 patient-years. The risk is not increased in metformin-treated patients. Metformin possesses a number of clinical effects independent of glucose reduction, including weight loss, which are beneficial to patients. The risk of death and cardiovascular disease is reduced by about a third in non-CKD patients. Since metformin intoxication undoubtedly causes LA, and metformin is renally excreted, inappropriate dosage of metformin will increase the risk of LA. It is suggested that introduction of metformin therapy to more advanced stages of CKD may bring therapeutic benefits that outweigh the possible risks.
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Boston Univ, Sch Med, Boston Collaborat Drug Surveillance Program, Lexington, MA USA
Boston Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02215 USAUniv Basel Hosp, Div Endocrinol Diabet & Clin Nutr, CH-4031 Basel, Switzerland
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Univ London Imperial Coll Sci Technol & Med, Diabet Unit, Sch Med, Chelsea & Westminster Hosp,Med Directorate, London SW10 9NH, EnglandUniv London Imperial Coll Sci Technol & Med, Diabet Unit, Sch Med, Chelsea & Westminster Hosp,Med Directorate, London SW10 9NH, England
Chan, NN
Brain, HPS
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Univ London Imperial Coll Sci Technol & Med, Diabet Unit, Sch Med, Chelsea & Westminster Hosp,Med Directorate, London SW10 9NH, EnglandUniv London Imperial Coll Sci Technol & Med, Diabet Unit, Sch Med, Chelsea & Westminster Hosp,Med Directorate, London SW10 9NH, England
Brain, HPS
Feher, MD
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Univ London Imperial Coll Sci Technol & Med, Diabet Unit, Sch Med, Chelsea & Westminster Hosp,Med Directorate, London SW10 9NH, EnglandUniv London Imperial Coll Sci Technol & Med, Diabet Unit, Sch Med, Chelsea & Westminster Hosp,Med Directorate, London SW10 9NH, England
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Boston Univ, Sch Med, Boston Collaborat Drug Surveillance Program, Lexington, MA USA
Boston Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02215 USAUniv Basel Hosp, Div Endocrinol Diabet & Clin Nutr, CH-4031 Basel, Switzerland
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Univ London Imperial Coll Sci Technol & Med, Diabet Unit, Sch Med, Chelsea & Westminster Hosp,Med Directorate, London SW10 9NH, EnglandUniv London Imperial Coll Sci Technol & Med, Diabet Unit, Sch Med, Chelsea & Westminster Hosp,Med Directorate, London SW10 9NH, England
Chan, NN
Brain, HPS
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Univ London Imperial Coll Sci Technol & Med, Diabet Unit, Sch Med, Chelsea & Westminster Hosp,Med Directorate, London SW10 9NH, EnglandUniv London Imperial Coll Sci Technol & Med, Diabet Unit, Sch Med, Chelsea & Westminster Hosp,Med Directorate, London SW10 9NH, England
Brain, HPS
Feher, MD
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Univ London Imperial Coll Sci Technol & Med, Diabet Unit, Sch Med, Chelsea & Westminster Hosp,Med Directorate, London SW10 9NH, EnglandUniv London Imperial Coll Sci Technol & Med, Diabet Unit, Sch Med, Chelsea & Westminster Hosp,Med Directorate, London SW10 9NH, England