Skip to main content
Log in

Twelve-month treatment with Liraglutide ameliorates Visceral Adiposity Index and common cardiovascular risk factors in type 2 diabetes outpatients

  • Original Article
  • Published:
Journal of Endocrinological Investigation Aims and scope Submit manuscript

Abstract

Aim

In addition to the effects on glycemic control and body weight, GLP-1 receptor agonists may favorably affect other major cardiovascular disease (CVD) risk factors, although currently available data are still sparse. In this retrospective study, we evaluated the effects of 12-month treatment with liraglutide on major CVD risk factors in 115 type 2 diabetes outpatients (60 men and 55 women), on stable hypoglycemic, anti-hypertensive and/or lipid-lowering therapy.

Methods

Clinical and anthropometric data, metabolic and lipid profile, as well as the Visceral Adiposity Index (VAI), an obesity-related CVD risk factor, were measured in all participants at baseline and after 12-month treatment.

Results

Treatment with liraglutide was associated with a significant reduction from baseline values of fasting blood glucose (−42.1 mg/dl, P < 0.05), HbA1c (−1.5 %, −17 mmol/mol, P < 0.05), body weight (−7.1 kg, P < 0.05), waist circumference (-6.8 cm, P < 0.001), total-cholesterol (−27.4 mg/dl, P < 0.05), LDL-cholesterol (−25.4 mg/dl, P < 0.05), triglycerides (−56.1 mg/dl, P < 0.05), and non-HDL-C (−36.6 mg/dl, P < 0.05) and an increase of HDL-cholesterol concentrations (+9.3 mg/dl, P < 0.001), a significant reduction in both systolic and diastolic blood pressure (−14.7 mmHg, P < 0.001 and −9.0 mmHg, P < 0.05, respectively) and a decrease of VAI values (−1.6, P < 0.001). All these differences were independent of changes in BMI and comparable in men and women.

Conclusions

In conclusion, 12-month treatment with liraglutide in add-on to on-going hypoglycemic therapy significantly ameliorates all major CVD risk factors and reduces cardiometabolic risk, as estimated by VAI values.

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.

Fig. 1

Similar content being viewed by others

Abbreviations

CVD:

Cardiovascular disease

T2D:

Type 2 diabetes

GLP-1RAs:

Glucagon-like peptide-1 receptor agonists

VAI:

Visceral Adiposity Index

References

  1. Wild S, Roglic G, Green A, Sicree R, King H (2004) Global prevalence of diabetes: estimates for the year 2000 and projections for 2030. Diabetes Care 27:1047–1053

    Article  PubMed  Google Scholar 

  2. Buse JB, Ginsberg HN, Bakris GL et al (2007) Primary prevention of cardiovascular diseases in people with diabetes mellitus: a scientific statement from the American Heart Association and the American Diabetes Association. Circulation 115:114–126

    Article  PubMed  Google Scholar 

  3. Liu SC, Tu YK, Chien MN, Chien KL (2012) Effect of antidiabetic agents added to metformin on glycaemic control, hypoglycaemia and weight change in patients with type 2 diabetes: a network meta-analysis. Diabetes Obes Metab 14:810–820

    Article  CAS  PubMed  Google Scholar 

  4. Drucker DJ, Nauck MA (2006) The incretin system: glucagonlike peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors in type 2 diabetes. Lancet 11(368):1696–1705

    Article  Google Scholar 

  5. Vilsbøll T, Christensen M, Junker AE, Knop FK, Gluud LL (2012) Effects of glucagon-like peptide-1 receptor agonists on weight loss: systematic review and meta-analyses of randomised controlled trials. BMJ 344:d7771

    Article  PubMed Central  PubMed  Google Scholar 

  6. Vilsbøll T, Garber AJ (2012) Non-glycaemic effects mediated via GLP-1 receptor agonists and the potential for exploiting these for therapeutic benefit: focus on liraglutide. Diabetes Obes Metab 14(Suppl 2):41–49

    Article  PubMed  Google Scholar 

  7. Marre M, Shaw J, Brändle M et al (2009) LEAD-1 SU study group. Liraglutide, a once-daily human GLP-1 analogue, added to a sulphonylurea over 26 weeks produces greater improvements in glycaemic and weight control compared with adding rosiglitazone or placebo in subjects with type 2 diabetes (LEAD-1 SU). Diabet Med 26:268–278

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  8. Nauck M, Frid A, Hermansen K et al (2013) Long-term efficacy and safety comparison of liraglutide, glimepiride and placebo, all in combination with metformin in type 2 diabetes: 2-year results from the LEAD-2 study. Diabetes Obes Metab 15:204–212

    Article  CAS  PubMed  Google Scholar 

  9. Garber A (2011) Henry RR, Ratner R, Hale P, Chang CT, Bode B; LEAD-3 (Mono) Study Group. Liraglutide, a once-daily human glucagon-like peptide 1 analogue, provides sustained improvements in glycaemic control and weight for 2 years as monotherapy compared with glimepiride in patients with type 2 diabetes. Diabetes Obes Metab 13:348–356

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  10. Zinman B, Gerich J, Buse JB et al (2009) LEAD-4 Study investigators. Efficacy and safety of the human glucagon-like peptide-1 analog liraglutide in combination with metformin and thiazolidinedione in patients with type 2 diabetes (LEAD-4 Met + TZD). Diabetes Care 32:1224–1230

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  11. Russell-Jones D, Vaag A, Schmitz O et al (2009) Liraglutide effect and action in diabetes 5 (LEAD-5) met + SU study group. Liraglutide vs insulin glargine and placebo in combination with metformin and sulfonylurea therapy in type 2 diabetes mellitus (LEAD-5 met + SU): a randomised controlled trial. Diabetologia 52:2046–2055

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  12. Buse JB, Rosenstock J, Sesti G et al (2009) LEAD-6 study group. Liraglutide once a day versus exenatide twice a day for type 2 diabetes: a 26-week randomised, parallel-group, multinational, open-label trial (LEAD-6). Lancet 374:39–47

    Article  CAS  PubMed  Google Scholar 

  13. Klonoff DC, Buse JB, Nielsen LL et al (2008) Exenatide effects on diabetes, obesity, cardiovascular risk factors and hepatic biomarkers in patients with type 2 diabetes treated for at least 3 years. Curr Med Res Opin 24:275–286

    CAS  PubMed  Google Scholar 

  14. Wang B, Zhong J, Lin H et al (2013) Blood pressure -lowering effects of GLP-1 receptor agonists exenatide and liraglutide: a meta-analysis of clinical trials. Diabetes Obes Metab 15:737–749

    Article  CAS  PubMed  Google Scholar 

  15. Inoue K, Maeda N, Kashine S et al (2011) Short-term effects of liraglutide on visceral fat adiposity, appetite, and food preference: a pilot study of obese Japanese patients with type 2 diabetes. Cardiovasc Diabetol 10:109

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  16. Amato MC, Giordano C, Galia M, AlkaMeSy Study Group et al (2010) Visceral Adiposity Index: a reliable indicator of visceral fat function associated with cardiometabolic risk. Diabetes Care 33:920–922

    Article  PubMed Central  PubMed  Google Scholar 

  17. Mohammadreza B, Farzad H, Davoud K, Fereidoun Prof AF (2012) Prognostic significance of the complex “Visceral Adiposity Index” vs. simple anthropometric measures: tehran lipid and glucose study. Cardiovasc Diabetol 11:20

    Article  PubMed Central  PubMed  Google Scholar 

  18. Robinson LE, Holt TA, Rees K, Randeva HS, O’Hare JP (2013) Effects of exenatide and liraglutide on heart rate, blood pressure and body weight: systematic review and meta-analysis. BMJ Open 3(1):e001986

    Article  PubMed Central  PubMed  Google Scholar 

  19. Evaluation of cardiovascular outcomes in patients with type 2 diabetes after acute coronary syndrome during treatment with AVE0010 (Lixisenatide) (ELIXA) http://clinicaltrials.gov/show/NCT01147250

  20. Friedewald WT, Levy RI, Fredrickson DS (1972) Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem 18(6):499–502

    CAS  PubMed  Google Scholar 

  21. Levey AS, Bosch JP, Lewis JB, Greene T, Rogers N, Roth D (1999) A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of diet in renal disease study group. Ann Intern Med 130:461–470

    Article  CAS  PubMed  Google Scholar 

  22. McCarthy MI (2010) Genomics, type 2 diabetes, and obesity. N Engl J Med 363:2339–2350

    Article  CAS  PubMed  Google Scholar 

  23. Niswender K, Pi-Sunyer X, Buse J et al (2013) Weight change with liraglutide and comparator therapies: an analysis of seven phase 3 trials from the liraglutide diabetes development programme. Diabetes Obes Metab 15:42–54

    Article  CAS  PubMed  Google Scholar 

  24. Fonseca V, Madsbad S, Falahati A et al (2009) Once-daily human GLP-1 analog liraglutide reduces systolic BP: a meta-analysis of 6 clinical trials (Abstract). Diabetes 58(Suppl):A146

    Google Scholar 

  25. Anagnostis P, Athyros VG, Adamidou F et al (2011) Glucagon-like peptide-1-based therapies and cardiovascular disease: looking beyond glycaemic control. Diabetes Obes Metab 13:302–312

    Article  CAS  PubMed  Google Scholar 

  26. Wang B, Ni Y, Zhong J, Sun F (2012) Effects of incretins on blood pressure: a promising therapy for type 2 diabetes mellitus with hypertension. J Diabetes 4:22–29

    Article  CAS  PubMed  Google Scholar 

  27. Choe HM, Townsend KA, Blount G, Lo CH, Sadowski L, Standiford CJ (2007) Treatment and control of blood pressure in patients with diabetes mellitus. Am J Health Syst Pharm 64:97–103

    Article  PubMed  Google Scholar 

  28. Sivertsen J, Rosenmeier J, Holst JJ, Vilsboll T (2012) The effect of glucagon-like peptide 1 on cardiovascular risk. Nat Rev Cardiol 9:209–222

    Article  CAS  PubMed  Google Scholar 

  29. Varanasi A, Patel P, Makdissi A, Dhindsa S, Chaudhuri A, Dandona P (2012) Clinical use of liraglutide in type 2 diabetes and its effect on cardiovascular risk factors. Endocrine Practice 18:140–145

    Article  PubMed  Google Scholar 

  30. Vilsbøll T, Zdravkovic M, Le Thi T et al (2007) Liraglutide, a long-acting human glucagon-like peptide-1 analog, given as monotherapy significantly improves glycemic control and lowers body weight without risk of hypoglycemia in patients with type 2 diabetes. Diabetes Care 30:1608–1610

    Article  PubMed  Google Scholar 

  31. Stein EA, Black DM (2002) Lipoprotein changes with statins. Curr Atheroscler Rep 4:14–18

    Article  PubMed  Google Scholar 

  32. Chehade JM, Alcalde R, Naem E, Mooradian AD, Wong NC, Haas MJ (2013) Induction of apolipoprotein A-I gene expression by glucagon-like peptide-1 and exendin-4 in hepatocytes but not intestinal cells. Metabolism 62:265–274

    Article  CAS  PubMed  Google Scholar 

  33. Amato MC, Giordano C, Pitrone M, Galluzzo A (2011) Cut-off points of the visceral adiposity index (VAI) identifying a visceral adipose dysfunction associated with cardiometabolic risk in a Caucasian Sicilian population. Lipids Health Dis 10:183

    Article  PubMed Central  PubMed  Google Scholar 

  34. Mulligan CM, Harper R, Harding J, McIlwaine W, Petruckevitch A, McLaughlin DM (2013) A retrospective audit of type 2 diabetes patients prescribed liraglutide in real-life clinical practice. Diabetes Ther 4:147–151

    Article  PubMed Central  PubMed  Google Scholar 

Download references

Conflict of interest

No conflicts of interest exist.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to G. T. Russo.

Additional information

G. T. Russo and A. M. Labate contributed equally to the manuscript.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOCX 35 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Russo, G.T., Labate, A.M., Giandalia, A. et al. Twelve-month treatment with Liraglutide ameliorates Visceral Adiposity Index and common cardiovascular risk factors in type 2 diabetes outpatients. J Endocrinol Invest 38, 81–89 (2015). https://doi.org/10.1007/s40618-014-0163-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40618-014-0163-9

Keywords

Navigation