Exp Clin Endocrinol Diabetes 2008; 116(2): 132-134
DOI: 10.1055/s-2007-984456
Short Communication

© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Clinical Benefit of a Short Term Dietary Oatmeal Intervention in Patients with Type 2 Diabetes and Severe Insulin Resistance: A Pilot Study

A. Lammert 1 , J. Kratzsch 2 , J. Selhorst 1 , P. M. Humpert 3 , A. Bierhaus 3 , R. Birck 1 , K. Kusterer 4 , H.-P. Hammes 1
  • 1V. Medizinische Klinik, University Hospital Mannheim, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany
  • 2ILM, University of Leipzig, Leipzig, Germany
  • 3Medizinische Klinik 1, University of Heidelberg, Heidelberg, Germany
  • 4Group Practice for Endocrinology, Mannheim, Germany
Further Information

Publication History

received 19.03.2007 first decision 31.05.2007

accepted 18.06.2007

Publication Date:
20 December 2007 (online)

Abstract

Aims/hypothesis: To evaluate the potential effectiveness of ‘carbohydrate days’ as a dietary intervention to overcome insulin resistance in type 2 diabetes.

Materials and Methods: Patients (n=14) with uncontrolled type 2 diabetes and insulin resistance as defined by a dosage of more than 1 IU/day*kg BW were consecutively enrolled in this prospective study. Primary outcomes were daily insulin requirement and mean blood glucose levels which were evaluated before, after, and 4 weeks after the intervention.

Results: All patients had a metabolic syndrome, 75% had microvascular and 57.1% macrovascular complications. Hospital setting and diabetes adapted diet alone led to improved glycemic control with a mean blood glucose 158±47 mg/dl. Intervention with two days of oatmeal diet further decreased mean blood glucose to 118±37 mg/dl (p<0.05). This was associated with a significant reduction of insulin dosage by 42.5% (before: 145±68.9 U/d, after 83±34.2 U/d, p<0.001) as well as a significant reduction (-26.4%, p<0.01) of serum leptin levels.After the four weeks outpatient period, insulin dosage remained significantly decreased (83±20.2 U/kg*d, p<0.01). Glycemic control was comparable (mean blood glucose141±20.78 mg/dl) to glucose levels within the hospital setting. Adiponectin levels increased significantly by 53.8% (p<0.05).

Conclusions: In this uncontrolled pilot study, hospital admission and diabetes adapted diet followed by oatmeal intervention achieved a ∼40% reduction of insulin dosage required to achieve controlled glucose levels. This effect was conserved after a 4 week outpatient phase with normal diet.

References

  • 1 Stumvoll M, Goldstein BJ, Haeften TW van. Type 2 diabetes: principles of pathogenesis and therapy.  Lancet. 2005;  365 1333-1346
  • 2 American College of Endocrinology American Diabetes Association. Consensus statement on inpatient diabetes glycemic control . A call to action. The ACE/ADA Task Force on Inpatient Diabetes.  Diab Care. 2006;  29 1955-1962
  • 3 UK Prospective Diabetes Study (UKPDS) Group . 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. 1998;  352 837-853
  • 4 Noorden C von. Ueber Hafercuren bei schwerem Diabetes mellitus.  Berl klin Wschr. 1903;  36 817-821
  • 5 Kadowaki T, Yamauchi T, Kubota N, Hara K, Ueki K, Tobe K. Adiponectin and adiponectin receptors in insulin resistance, diabetes, and the metabolic syndrome.  J Clin Invest. 2006;  116 1784-1792
  • 6 Boden G, Markku L. Lipids and glucose in type 2 diabetes: What is the cause and effect?.  Diab Care. 2004;  27 2253-2259
  • 7 Inzucchi SE. Management of hyperglycemia in the hospital setting.  N Engl J Med. 2006;  355 1903-1911
  • 8 Kratzsch J, Berthold A, Lammert A, Reuter W, Keller E, Kiess W. A rapid, quantitative immunofunctional assay for measuring human leptin.  Horm Res. 2002;  57 127-132
  • 9 Tuomilehto J, Lindstrom J, Eriksson JG, Valle TT, Hamalainen H, Ilanne-Parikka P, Keinanen-Kiukaanniemi S, Laakso M, Louheranta A, Rastas M, Salminen V. Uusitupa M, Finnish Diabetes Prevention Study Group . Prevention of type 2 diabetes mellitus by changes in lifestyle among subjects with impaired glucose tolerance.  N Engl J Med. 2001;  344 1343-1350
  • 10 Qi L, Meigs JB, Liu S, Manson JE, Mantzoros CS, Hu FB. Dietary fibers and glycemic load, obesity, and plasma adiponectin levels in women with type 2 diabetes.  Diab Care. 2006;  29 1501-1505
  • 11 Lindström J, Ilanne-Parikka P, Peltonen M, Aunola S, Eriksson JG, Hemiö K, Hämäläinen H, Härkönen P, Keinänen-Kiukaanniemi S, Laakso M, Louheranta A, Mannelin M, Paturi M, Sundvall J, Valle TT, Uusitupa M, Tuomilehto J. on behalf of the Finnish Diabetes Prevention Study Group . Sustained reduction in the incidence of type 2 diabetes by lifestyle intervention: follow-up of the Finnish Diabetes Prevention Study.  Lancet. 2006;  368 1673-1679
  • 12 Weickert MO, Mohlig M, Koebnick C, Holst JJ, Namsolleck P, Ristow M, Osterhoff M, Rochlitz H, Rudovich N, Spranger J, Pfeiffer AF. Impact of cereal fibre on glucose-regulating factors.  Diabetologia. 2005;  48 2343-2353
  • 13 Weickert MO, Mohlig M, Schofl C, Arafat AM, Otto B, Viehoff H, Koebnick C, Kohl A, Spranger J, Pfeiffer AF. Cereal fiber improves whole-body insulin sensitivity in overweight and obese women.  Diabetes Care. 2006;  29 775-780
  • 14 Stefan N, Stumvoll M, Vozarova B, Weyer C, Funahashi T, Matsuzawa Y, Bogardus C, Tataranni A. Plasma adiponectin and endogenous glucose production in humans.  Diab Care. 2003;  26 3315-3319
  • 15 Tschritter O, Fritsche A, Thamer C, Haap M, Shirkavand F, Rahe S, Staiger H, Maerker E, Haring H, Stumvoll M. Plasma adiponectin concentrations predict insulin sensitivity of both glucose and lipid metabolism.  Diabetes. 2003;  52 239-243
  • 16 Rigalleau V, Rabemanantsoa C, Gin H. A three-day insulin-induced normoglycemia improves carbohydrate oxidation in type 2 diabetic subjects.  Metab. 2002;  51 1484-1488

Correspondence

A. LammertMD 

V. Medizinische Klinik

University Hospital Mannheim

Theodor-Kutzer-Ufer 1-3

68167 Mannheim

Germany

Phone: +49/621/383 33 70

Fax: +49/621/383 21 69

Email: alexander.lammert@med5.ma.uni-heidelberg.de

    >