[Metabolic syndrome and hormonal interaction in obese and type 2 diabetic Algerian subject: the behavior eating disorder impact]

Ann Biol Clin (Paris). 2009 May-Jun;67(3):315-23. doi: 10.1684/abc.2009.0326.
[Article in French]

Abstract

Background: These twenty last years, the metabolic syndrome was accused in various human pathologies including android obesity and type 2 diabetes. In obesity, increased body weight is frequently associated with excessive caloric food and sedentary activities. The Behaviour Eating Disorders (BED) is involved in over-consumption alimentary. In Algeria, we observed increasingly deviations in life-style alimentary, from the Mediterranean-Cretan model to American fast-food model.

Aim: To study interactions between the BED, hormonal secretions and metabolic syndrome parameters.

Methods: The present study was undertaken on Algerian population cohorts composed of 30 obese subjects, 70 type 2 diabetic patients and 30 healthy subjects. The BED was evaluated by TFEQ and DEBQ tests. Anthropometric parameters (waist circumference, IMC), metabolic parameters (glucose, triglycerides, HDL-C, LDL-C) and hormones (insulin, peptide C, ACTH, cortisol, GH) were determinates by biometrics, spectrophotometry and radioimmunology methods, respectively.

Results: Multivariate analyses showed the high correlation between the BED and the metabolic syndrome, particularly a critical insulinoresistance state (IR). This IR generates in periphery a whole of metabolic disorders: dyslipidemia, hyperglycemia and hypertrophy of adipose tissue. In diabetic and obese patients, cortisol, ACTH and GH secretions are insidiously altered and to lead metabolic disorders.

Conclusion: In this study, the role of the BED in obesity and diabetes genesis seems to be confirmed. In response to nutritional stress, the BED generates a hyperactivity of endocrine pancreas, adrenal gland, and pituitary gland. It appeared that Algerian population is not adapted to fast-food American model.

MeSH terms

  • Adipose Tissue / pathology
  • Adult
  • Algeria
  • Blood Glucose / metabolism
  • Body Weight
  • Cholesterol / blood
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / complications*
  • Diabetes Mellitus, Type 2 / physiopathology*
  • Feeding Behavior / physiology*
  • Feeding and Eating Disorders / blood
  • Feeding and Eating Disorders / complications
  • Feeding and Eating Disorders / physiopathology*
  • Female
  • Fructosamine / blood
  • Human Growth Hormone / blood
  • Humans
  • Male
  • Metabolic Syndrome / blood
  • Metabolic Syndrome / physiopathology*
  • Middle Aged
  • Multivariate Analysis
  • Obesity / blood
  • Obesity / complications*
  • Obesity / physiopathology*
  • Peptides / blood
  • Triglycerides / blood
  • Waist Circumference

Substances

  • Blood Glucose
  • Peptides
  • Triglycerides
  • polypeptide C
  • Human Growth Hormone
  • Fructosamine
  • Cholesterol