Skip to main content
Log in

Orale Diabetestherapie

Welche Substanz ist wann indiziert?

Oral diabetes treatment: Which substance is indicated at which time?

  • Schwerpunkt: Was ist gesichert in der Therapie?
  • Published:
Der Internist Aims and scope Submit manuscript

Zusammenfassung

Die Prävalenz des Typ-2-Diabetes zeigt in Deutschland weiterhin eine deutlich steigende Tendenz. Was in früheren Zeiten als „harmloser Alterszucker“ galt, wird zunehmend als Erkrankung mit hohem Risiko für vaskuläre Folgeschäden und eine Verkürzung der verbleibenden Lebenserwartung erkannt, sofern keine adäquate Therapie erfolgt. Neben der Korrektur einer Hyperglykämie gehört hierzu die konsequente Behandlung begleitender Risikofaktoren, wie Hypertonie, Dyslipidämie sowie Adipositas infolge Fehlernährung und Bewegungsmangel. Bei der großen Mehrzahl von übergewichtigen Typ-2-Diabetikern ist Metformin das orale Antidiabetikum der ersten Wahl, sofern nicht die wichtige Kontraindikation einer Niereninsuffizienz besteht. Im Gegensatz zu dieser durch eine Endpunktstudie abgesicherten Empfehlung für die Monotherapie übergewichtiger Typ-2-Diabetiker gibt es bisher keine gleichwertige Evidenz für eine der möglichen Optionen einer oralen Kombinationstherapie.

Abstract

The prevalence of type 2 diabetes continues to show a clear upward trend in Germany. In earlier days it was considered the “harmless diabetes of old age,” but has become increasingly recognized as a disease carrying a high risk of vascular sequelae as well as shortening the diabetic’s remaining life expectancy if adequate therapy is not initiated. In addition to correcting hyperglycemia, treatment consists in effective management of concomitant risk factors such as hypertension, dyslipidemia, and adiposity resulting from faulty nutrition and lack of exercise. In the large majority of overweight type 2 diabetics, metformin is the oral antidiabetic agent of first choice provided the patient does not exhibit renal insufficiency, which represents the most important contraindication. This recommendation for monotherapy of overweight type 2 diabetics is supported by an endpoint study. In contrast, no equivalent evidence is available on any of the possible options for oral combination therapy.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Literatur

  1. Petersen KF, Dufour S, Befroy D, Garcia R, Shulman GI (2004) Impaired mitochondrial activity in the insulin-resistant offspring of patients with type 2 diabetes. N Engl J Med 350: 664–671

    Google Scholar 

  2. Pickup JC (2004) Inflammation and activated innate immunity in the pathogenesis of type 2 diabetes. Diabetes Care 27: 813–823

    PubMed  Google Scholar 

  3. UK Prospective Diabetes Study (UKPDS) Group (1998) Effect of intensive blood-glucose control with metformin on complications in overweight patients with type 2 diabetes (UKPDS 34). Lancet 352: 854–865

    Article  PubMed  Google Scholar 

  4. UK Prospective Diabetes Study (UKPDS) Group (1998) Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). Lancet 352: 837–853

    Article  PubMed  Google Scholar 

  5. Gaede P, Vedel P, Larsen N, Jensen GV, Parving HH, Pedersen O (2003) Multifactorial intervention and cardiovascular disease in patients with type 2 diabetes. N Engl J Med 348: 383–393

    Article  PubMed  Google Scholar 

  6. Häring H, Joost H, Laube H, Matthaei S, Meissner H, Panten U, Schernthaner G (2003) Antihyperglykämische Therapie des Diabetes mellitus Typ 2. Evidenzbasierte Diabetes-Leitlinie DDG. Diab Stoffw 12: 13–31

    Google Scholar 

  7. ❚❚❚❚❚❚❚❚ (2002) Nationale Versorgungs-Leitlinie Diabetes mellitus Typ 2. Z Arztl Fortbild Qualitatssich 96 [Suppl 2]: 1–23

  8. Manley SE, Stratton IM, Cull CA et al. (2000) Effects of three months‘ diet after diagnosis of Type 2 diabetes on plasma lipids and lipoproteins (UKPDS 45). UK Prospective Diabetes Study Group. Diabet Med 17: 518–523

    Article  CAS  PubMed  Google Scholar 

  9. Boule NG, Haddad E, Kenny GP et al. (2001) Effects of exercise on glycemic control and body mass in type 2 diabetes mellitus: a meta-analysis of controlled clinical trials. JAMA 286: 1218–1227

    CAS  PubMed  Google Scholar 

  10. Turner RC, Cull CA, Frighi V, Holman RR (1999) Glycemic control with diet, sulfonylurea, metformin, or insulin in patients with type 2 diabetes mellitus: progressive requirement for multiple therapies (UKPDS 49). UK Prospective Diabetes Study (UKPDS) Group. JAMA 281: 2005–2012

    CAS  PubMed  Google Scholar 

  11. Inzucchi SE (2002) Oral antihyperglycemic therapy for type 2 diabetes: scientific review. JAMA 287: 360–372

    CAS  PubMed  Google Scholar 

  12. Matthaei S, Stumvoll M, Kellerer M, Haring HU (2000) Pathophysiology and pharmacological treatment of insulin resistance. Endocr Rev 21: 585–618

    Article  CAS  PubMed  Google Scholar 

  13. Hundal RS, Inzucchi SE (2003) Metformin: new understandings, new uses. Drugs 63: 1879–1894

    CAS  PubMed  Google Scholar 

  14. Emslie-Smith AM, Boyle DI, Evans JM, Sullivan F, Morris AD (2001) Contraindications to metformin therapy in patients with Type 2 diabetes—a population-based study of adherence to prescribing guidelines. Diabet Med 18: 483–488

    Article  CAS  PubMed  Google Scholar 

  15. Salpeter S, Greyber E, Pasternak G, Salpeter E (2003) Risk of fatal and nonfatal lactic acidosis with metformin use in type 2 diabetes mellitus. Cochrane Database Syst Rev CD002967

  16. Klepzig H, Kober G, Matter C et al. (1999) Sulfonylureas and ischaemic preconditioning, a double-blind, placebo-controlled evaluation of glimepiride and glibenclamide. Eur Heart J 20: 439–446

    Article  CAS  PubMed  Google Scholar 

  17. Schiekofer S, Rudofsky G, Andrassy M et al. (2003) Glimepiride reduces mononuclear activation of the redox-sensitive transcription factor nuclear factor-kappa B. Diabetes Obes Metab 5: 251–261

    Article  CAS  PubMed  Google Scholar 

  18. Rosenstock J, Hassman DR, Madder RD, Brazinsky SA, Farrell J, Khutoryansky N, Hale PM (2004) Repaglinide versus nateglinide monotherapy: a randomized, multicenter study. Diabetes Care 27: 1265–1270

    CAS  PubMed  Google Scholar 

  19. Hasslacher C (2003) Safety and efficacy of repaglinide in type 2 diabetic patients with and without impaired renal function. Diabetes Care 26: 886–891

    CAS  PubMed  Google Scholar 

  20. Chiasson JL, Josse RG, Gomis R, Hanefeld M, Karasik A, Laakso M (2004) Acarbose for the prevention of Type 2 diabetes, hypertension and cardiovascular disease in subjects with impaired glucose tolerance: facts and interpretations concerning the critical analysis of the STOP-NIDDM Trial data. Diabetologia 47: 969–975

    Article  CAS  PubMed  Google Scholar 

  21. Holman RR, Cull CA, Turner RC (1999) A randomized double-blind trial of acarbose in type 2 diabetes shows improved glycemic control over 3 years (U.K. Prospective Diabetes Study 44). Diabetes Care 22: 960–964

    CAS  PubMed  Google Scholar 

  22. Diamant M, Heine RJ (2003) Thiazolidinediones in type 2 diabetes mellitus: current clinical evidence. Drugs 63: 1373–1405

    CAS  PubMed  Google Scholar 

  23. Buse JB, Tan MH, Prince MJ, Erickson PP (2004) The effects of oral anti-hyperglycaemic medications on serum lipid profiles in patients with type 2 diabetes. Diabetes Obes Metab 6: 133–156

    Article  CAS  PubMed  Google Scholar 

  24. van Wijk JP, de Koning EJ, Martens EP, Rabelink TJ (2003) Thiazolidinediones and blood lipids in type 2 diabetes. Arterioscler Thromb Vasc Biol 23: 1744–1749

    Article  PubMed  Google Scholar 

  25. Neuschwander-Tetri BA, Brunt EM, Wehmeier KR, Oliver D, Bacon BR (2003) Improved nonalcoholic steatohepatitis after 48 weeks of treatment with the PPAR-gamma ligand rosiglitazone. Hepatology 38: 1008–1017

    Article  CAS  PubMed  Google Scholar 

  26. Promrat K, Lutchman G, Uwaifo GI et al. (2004) A pilot study of pioglitazone treatment for nonalcoholic steatohepatitis. Hepatology 39: 188–196

    Article  CAS  PubMed  Google Scholar 

  27. Hanefeld M, Brunetti P, Schernthaner GH, Matthews DR, Charbonnel BH (2004) One-year glycemic control with a sulfonylurea plus pioglitazone versus a sulfonylurea plus metformin in patients with type 2 diabetes. Diabetes Care 27: 141–147

    CAS  PubMed  Google Scholar 

  28. Raskin P, Klaff L, McGill J, South SA, Hollander P, Khutoryansky N, Hale PM (2003) Efficacy and safety of combination therapy: repaglinide plus metformin versus nateglinide plus metformin. Diabetes Care 26: 2063–2068

    CAS  PubMed  Google Scholar 

  29. Malmberg K (1997) Prospective randomised study of intensive insulin treatment on long term survival after acute myocardial infarction in patients with diabetes mellitus. DIGAMI (Diabetes Mellitus, Insulin Glucose Infusion in Acute Myocardial Infarction) Study Group. BMJ 314: 1512–1515

    CAS  PubMed  Google Scholar 

  30. Grundy SM, Cleeman JI, Merz CN et al. (2004) Implications of recent clinical trials for the National Cholesterol Education Program Adult Treatment Panel III guidelines. Circulation 110: 227–239

    Article  PubMed  Google Scholar 

Download references

Interessenkonflikt:

Der korrespondierende Autor versichert, dass keine Verbindungen mit einer Firma, deren Produkt in dem Artikel genannt ist, oder einer Firma, die ein Konkurrenzprodukt vertreibt, bestehen.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. Hamann.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hamann, A., Morcos, M. & Nawroth, P. Orale Diabetestherapie. Internist 45, 1356–1363 (2004). https://doi.org/10.1007/s00108-004-1306-4

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00108-004-1306-4

Schlüsselwörter

Keywords

Navigation