The innate immune response and type 2 diabetes: evidence that leptin is associated with a stress-related (acute-phase) reaction

Citation
Jc. Pickup et al., The innate immune response and type 2 diabetes: evidence that leptin is associated with a stress-related (acute-phase) reaction, CLIN ENDOCR, 52(1), 2000, pp. 107-112
Citations number
31
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
CLINICAL ENDOCRINOLOGY
ISSN journal
03000664 → ACNP
Volume
52
Issue
1
Year of publication
2000
Pages
107 - 112
Database
ISI
SICI code
0300-0664(200001)52:1<107:TIIRAT>2.0.ZU;2-E
Abstract
OBJECTIVE Leptin is produced by adipose tissue and controls food intake and body weight. Although blood levels of leptin reflect energy stores, cytoki nes also stimulate leptin production from fat. Because we have proposed tha t type 2 diabetes mellitus is associated with a cytokine-mediated acute-pha se or stress response, part of the innate immune system, we sought evidence that leptin is increased in type 2 diabetes partly as a stress response, i ndependently of obesity and sex. DESIGN We selected two groups of type 2 diabetic patients with either a low acute-phase response (< 2.30 mmol/l serum concentration of the acute-phase marker sialic acid) or high response (> 2.30 mmol/l sialic acid), but pair -matched for body mass index (BMI) and sex. PATIENTS Twenty type 2 diabetic subjects (11 male, 9 female) in each group, whose body mass index (BMI) and age were comparable (mean +/- SD: 28.8 +/- 3.8 vs. 28.9 +/- 3.8 kg/m(2), and 60.7 +/- 8.9 vs. 61.9 +/- 12.3 years, lo w vs. high acute-phase responders, respectively). The glycaemic control was also similar in each group (glycated haemoglobin: 9.1 +/- 2.2 vs. 8.9 +/- 1.9%). MEASUREMENTS Serum concentrations of sialic acid, leptin, interleukin-6 (IL -6) (the major cytokine mediator of the acute-phase response) and cortisol were assayed in fasting venous blood samples from patients and the results compared. RESULTS Serum leptin concentration was increased in the high compared to th e low acute-phase group (median 13.2 (range 3.6-55) vs. 8.1 (2.0-22.5) mu g /l, P = 0.004). IL-6 and cortisol concentrations were also higher in the hi gh-stress group (1.9 (1.0-6.4) vs. 1.4 (0.4-7.5) ng/l, P = 0.02; and 409 (1 80-875) vs. 290 (157-705) nmol/l, P = 0.02, respectively). Leptin was stron gly correlated with BMI (r = 0.61, P < 0.001), but also with sialic acid (r = 0.40, P = 0.01) and IL-6 (r = 0.38, P = 0.04). CONCLUSIONS Serum leptin concentrations in type 2 diabetes are partly relat ed to an acute-phase or stress response, independent of BMI and sex. The as sociation of hyperleptinaemia with elevated serum cortisol provides a mecha nism for leptin resistance in type 2 diabetes (glucocorticoids inhibit the central action of leptin). This study provides further support for the theo ry that type 2 diabetes is asociated with chronic innate immune activation.