Association between metformin use and below-the-knee arterial calcification score in type 2 diabetic patients
- Aurélien Mary1, 2, 3Email author,
- Agnes Hartemann4, 5, 6, 7,
- Sophie Liabeuf1, 3, 8,
- Carole Elodie Aubert6, 9,
- Salim Kemel5, 10, 11,
- Joe Elie Salem5, 7, 12, 13,
- Philippe Cluzel5, 10, 11,
- Aurélie Lenglet1, 2, 3,
- Ziad A. Massy14, 15, 16,
- Jean-Daniel Lalau1, 17, 18,
- Romuald Mentaverri1, 3, 19,
- Olivier Bourron†4, 5, 6, 7 and
- Saïd Kamel†1, 3, 20Email author
© The Author(s) 2017
Received: 15 December 2016
Accepted: 5 February 2017
Published: 15 February 2017
Vascular calcification (VC) is common in type 2 diabetes, and is associated with cardiovascular complications. Recent preclinical data suggest that metformin inhibits VC both in vitro and in animal models. However, metformin’s effects in patients with diabetic VC have not previously been characterized. The present study investigated the association between metformin use and lower-limb arterial calcification in patients with type 2 diabetes and high cardiovascular risk.
The DIACART cross-sectional cohort study included 198 patients with type 2 diabetes but without severe chronic kidney disease. Below-the-knee calcification scores were assessed by computed tomography and supplemented by colour duplex ultrasonography. Data on anti-diabetic drugs were carefully collected from the patients’ medical records and during patient interviews. Biochemical and clinical data were studied as potential confounding factors.
Metformin-treated patients had a significantly lower calcification score than metformin-free patients (mean ± standard deviation: 2033 ± 4514 and 4684 ± 9291, respectively; p = 0.01). A univariate analysis showed that metformin was associated with a significantly lower prevalence of severe below-the-knee arterial calcification (p = 0.02). VC was not significantly associated with the use of other antidiabetic drugs, including sulfonylureas, insulin, gliptin, and glucagon like peptide-1 analogues. A multivariate logistic regression analysis indicated that the association between metformin use and calcification score (odds ratio [95% confidence interval] = 0.33 [0.11–0.98]; p = 0.045) was independent of age, gender, tobacco use, renal function, previous cardiovascular disease, diabetes duration, neuropathy, retinopathy, HbA1c levels, and inflammation.
In patients with type 2 diabetes, metformin use was independently associated with a lower below-the-knee arterial calcification score. This association may contribute to metformin’s well-known vascular protective effect. Further prospective investigations of metformin’s potential ability to inhibit VC in patients with and without type 2 diabetes are now needed to confirm these results.
KeywordsOral pharmacological agents Macrovascular disease Imaging (MRI/PET/other) Biological statistics Clinical science Human Clinical science and care (all)
Vascular calcification (VC) corresponds to the pathological deposition of calcium-phosphate crystals in the vasculature, causing several adverse cardiovascular effects. Indeed, it is now clearly established that VC is associated with cardiovascular mortality (independently of other risks factors) in the general population and in patients with type 2 diabetes [1, 2]. Type 2 diabetes is known to induce VC, principally at the media tunica of the artery (medial calcific sclerosis) [3, 4]. Medial calcification principally occurs in patients with neuropathy , and tibial artery calcification contributes to peripheral artery occlusive disease—a leading risk factor for amputation in type 2 diabetes . Hence, limiting or decreasing arterial wall calcification is an important therapeutic objective in patients with types 2 diabetes. However, medications specifically aimed at avoiding or delaying VC are not available.
On the cellular level, VC is an active process that involves many different stimuli and signalling pathways. Vascular smooth muscle cells (VSMCs) or circulating myeloid cells express bone-related proteins (such as Runx2, Msx2, and osteocalcin) and ultimately differentiate into osteoblast-like cells [4, 7–9]. Beyond the preponderant role of calcium and phosphate homeostasis in VC, several specific factors have been associated with increased VC in patients with type 2 diabetes, such as high glucose concentration , advanced glycation end products , increased activity of the renin angiotensin system , and diabetic nephropathy . The involvement of these specific mechanisms suggests that medications aimed at controlling hyperglycaemia could protect against VC. Some studies have indeed reported a positive relationship between HbA1c levels on one hand and the coronary artery calcium score [14–16] and peripheral vascular calcification  on the other.
With regard to anti-diabetic medications, recently published data have highlighted metformin’s potential ability to reduce VC. In in vitro studies, exposure of rat aortic VSMCs to metformin was associated with a significant reduction in trans differentiation and calcium deposition via the activation of AMP-activated protein kinase (AMPK) and endothelial nitric oxide synthase (eNOS) . These results were confirmed in vivo in rats treated with vitamin D and nicotine, in which metformin reduced VC by restoring AMPK phosphorylation and eNOS expression . Cai et al. described the underlying molecular mechanism in more detail in dual ApoE and AMPK1α1 knock-out mice; activation of AMPK1α1 in VSMCs was the main factor involved in metformin’s inhibition of atherosclerotic calcification .
On the basis of these preclinical findings, we hypothesized that metformin use could be associated with lower levels of VC in patients with type 2 diabetes. We therefore decided to study the association between metformin use and the below-the-knee arterial calcification score in a population of patients with type 2 diabetes.
Research design and methods
The protocol of the DIACART Study (for “Diabète et Calcification Arterielle”) has been described in detail elsewhere . In brief, the study included 198 patients with type 2 diabetes attending the Cardiology and Diabetology Departments at Pitié-Salpêtrière University Hospital (Paris, France) over an 8-month period (from November 2011 to July 2012). The main inclusion criteria were (i) type 2 diabetes, and (ii) high cardiovascular risk. This risk was defined as the presence of one or more of the following factors: coronary artery disease, peripheral arterial occlusive disease, and age >50 years (for men) or >60 years (for women). The main exclusion criteria were (i) stage 4 or more chronic kidney disease, defined as a glomerular filtration rate estimated according to the Modification of Diet in Renal Disease equation (eGFR-MDRD) ≤30 ml/min , (ii) type 1 diabetes, (iii) a history of lower-limb angioplasty or bypass. The study was performed in accordance with the principles of the Declaration of Helsinki. The study protocol was approved by the local independent ethic committee (Comité de Protection des Personnes “Ile de France VI”, Paris, France). Patients were provided with comprehensive information on the study’s objectives and procedures. All patients gave their written, informed consent to participation.
Clinical evaluations, laboratory blood and urine tests, multislice spiral CT scans, colour duplex ultrasonography, and an interview focused on the patient’s treatments and comorbidities were performed during a 1-day hospitalization. Additional information on anti-diabetic drugs use was extracted from the patients’ medical records. All data were analyzed independently by physicians blinded to the patients’ other results. Peripheral neuropathy was evaluated according to the Neuropathy Disability Score (with a score ≥6 considered to be abnormal). Previous cardiovascular disease was defined as a history of myocardial infarction, stroke, or any invasive procedure for coronary artery disease.
Quantification of below-the-knee artery calcification
Below-the-knee artery calcification was assessed by scanning in the craniocaudal direction (from the patella to the ankle) with a 128-slice multi detector CT system (Somatom Definition Flash, Siemens Healthcare, Forchheim, Germany) in the absence of contrast agent. Each 3-mm cross-sectional slice was individually analyzed with Heartbeat CaScore software (Philips Healthcare, Eindhoven, The Netherlands). Each 1 mm2 area along below-the-knee arteries with ≥130 Hounsfield units was identified and multiplied by its density score (from 1 to 4). The sum of the weighted areas was used to calculate the calcification score, according to Agatston’s method . Calcification scores for the main below-the-knee arteries (the distal popliteal, anterior tibial, posterior tibial, and peroneal arteries) were summed to give an overall calcification score.
Quantification of peripheral arterial occlusion and medial calcific sclerosis
Colour duplex ultrasonography was used to comprehensively assess VC. Peripheral arterial occlusive disease was defined as occlusion or >70% stenosis in any artery from the abdominal tree down to the foot arteries. The severity of the stenosis was rated, with a score of 0 for no stenosis or <70% stenosis, a score of 2 for >70% stenosis, and a score of 3 for occlusion. The overall occlusion score (ranging from 0 to 39) was obtained by summing each individual artery score. Medial calcific sclerosis was also graded on the basis of ultrasound imaging, with a score of 0 point if not visible, a score of 1 if discontinuous, a score of 2 if continuous, and a score of 3 if the lumen was obstructed. Using the same method, an overall lower-limb medial calcific sclerosis score was calculated (ranging from 0 to 36).
Fasting blood were collected for measurement of HbA1c, glucose, ultrasensitive C-reactive protein, interleukin 6 (IL-6), calcium, phosphate, creatinine, and urine samples for measurement of microalbuminuria.
Data are expressed as the mean ± standard deviation (SD) and median for quantitative variables or the number (percentage) for qualitative variables. Given that the calcification scores were not normally distributed, a semi-log scale was used for graphical representations. The study population was divided into metformin-treated and -non-treated groups, depending on the current prescription. Intergroup comparisons were performed with a χ2 test for qualitative variables, and Student’s T test or the Mann–Whitney test for continuous variables. χ2 tests were also used to compare the frequency of metformin prescription in calcification score tertiles. For logistic regression analyses, patients were divided into two groups as a function of the severity of below-the-knee calcification (a score of 0–166 Agatston units [corresponding to the first tertile] vs. a score of >166). Univariate logistic regression analyses were used to assess the association between the below-the-knee calcification score category and metformin use. To assess the independence of this association (particularly with regard to age and renal status), we performed a multivariate logistic regression that included both variables identified in univariate analyses and relevant clinical variables. Markers of the severity of diabetes (the duration of diabetes, a history of retinopathy or neuropathy, the HbA1c level, and insulin treatment) were always entered as potential factors explaining the intensity of calcification. Furthermore, the likelihood ratio technique was used to test the model’s robustness. Patients with missing data were excluded solely from analyses in which the corresponding parameter was specifically included. For all tests, the threshold for statistically significance was set to p ≤ 0.05. All statistical analyses were performed using SPSS software (version 18.0, SPSS Inc., Chicago, IL, USA). Graphs were created using SPSS software (version 18.0, SPSS Inc., Chicago, IL, USA) or GraphPad Prism (version 5.0, GraphPad Software, La Jolla California, USA).
Demographic characteristics of the total study population and the metformin subgroups
64.4 ± 8.4 (65)
63.8 ± 8.2 (64)
66.9 ± 9 (66)
Diabetes duration (y)
14.6 ± 9.3 (13)
14.7 ± 9.1 (13)
14.2 ± 10.6 (12)
Body mass index (kg/m2)
29.2 ± 5.3 (28.0)
29.1 ± 5.2 (28.2)
29.3 ± 5.4 (29.4)
Current or ex-smoker
Calcification score (AU)
2528 ± 5779 (524)
2033 ± 4514 (434)
4684 ± 9291 (1044)
19.1 ± 10.9 (24)
18 ± 10.7 (20)
23.6 ± 10.8 (24)
3.5 ± 5.3 (0)
3.2 ± 5.1 (0)
4.6 ± 6.1 (3)
76 ± 20 (76)
77 ± 20 (77)
70 ± 18 (71)
166 ± 841 (23)
178 ± 924 (23)
110 ± 255 (17)
7.8 ± 1.5 (7.5)/62 ± 16 (58)
7.8 ± 1.4 (7.5)/62 ± 15 (58)
8.0 ± 1.7 (7.5)/64 ± 19 (58)
Blood glucose (mmol/l)
8.2 ± 2.8 (7.8)
8.2 ± 2.8 (7.8)
7.9 ± 2.8 (7.6)
2.32 ± 0.11 (2.32)
2.32 ± 0.11 (2.32)
2.31 ± 0.14 (2.31)
1.02 ± 0.15 (1.02)
1.02 ± 0.15 (1.02)
1.04 ± 0.17 (1.02)
2.2 ± 2.5 (1.2)
2.1 ± 2.4 (1.2)
2.7 ± 2.9 (1.5)
5.1 ± 22.2 (2.9)
3.5 ± 3.6 (2.8)
12.4 ± 50.5 (3.3)
LDL cholesterol (g/l)
1.93 ± 0.74 (1.81)
1.93 ± 0.76 (1.78)
2.04 ± 0.67 (1.89)
HDL cholesterol (g/l)
1.08 ± 0.33 (1.06)
1.06 ± 0.34 (1.01)
1.15 ± 0.28 (1.17)
1.58 ± 1.05 (1.26)
1.62 ± 1.11 (1.24)
1.42 ± 0.72 (1.42)
Association between below-the-knee calcification scores and metformin treatment
Independence of the association between metformin prescription and VC
The present study is the first to demonstrate that metformin prescription in patients with type 2 diabetes is associated with lower levels of below-the-knee arterial calcification. This association was found to be independent of age, gender, renal function, diabetes duration and complications of diabetes. The majority of study participants (81.3%) were taking metformin; this reflects compliance with current guidelines on diabetes treatment and trends in the prescription of antidiabetic drugs . Despite the fact that the number of patients not receiving metformin was rather small, it should be noted that the association between metformin use and lower calcification remained statistically significant in a multivariate analysis. Moreover, none of the other antidiabetic drugs taken were significantly associated with the calcification scores—suggesting that this property is specific to metformin.
The American Diabetes Association and European Association for the Study of Diabetes both recommend metformin as the first-line pharmacological treatment for type 2 diabetes , in view of the drug’s association with lower cardiovascular morbidity and mortality rates . The results of the UK Prospective Diabetes Study showed that early intervention with metformin in patients with type 2 diabetes decreased the all-cause mortality rate by 36% (due to a decrease in macrovascular events) . Metformin treatment in type 2 diabetes patients was effective in reducing the carotid intima-media thickness [28, 29] and is even associated with lower mortality rates in patients with established atherothrombosis . Interestingly, metformin treatment has been shown to increase lower arterial flow in diabetes-free patients with peripheral vascular disease —suggesting that the drug’s protective cardiovascular effect is not solely due to its action on blood glucose levels. The mechanisms involved in metformin-mediated cardiovascular protection have not yet been fully characterized. On the molecular level, it has been suggested that activation of AMPK might have a central role. AMPK phosphorylation by metformin improves the lipid profile , decreases oxidative stress , and protects against ischemia by maintaining ATP energy balance and increasing eNOS activity . Recently published data show that metformin has a protective effect on endothelial function and angiogenesis. In streptozotocin-induced diabetic mice, metformin improved the function and increased the number of bone marrow endothelial progenitor cells (EPCs) . This result has been confirmed in patients with type 1 diabetes in the MERIT study . In cellular models of diabetes, metformin’s pro-angiogenic endothelial properties were found to be related to (i) AMPK/eNOS activity , (ii) a decrease in miR-34a levels and an increase in sirtuin1 expression , and (iii) secretion of vascular endothelial growth factor A together with a reduction in mRNA levels of angiogenetic inhibitors . It was recently hypothesized that the EPCs’ loss of proangiogenic function in type 1 and 2 diabetes may lead to an osteogenic shift to myeloid calcifying cells, which thus links endothelial dysfunction and VC .
Vascular calcification is also associated with higher cardiovascular morbidity in patients with diabetes . A putative metformin-related decrease in VC may thus contribute to cardiovascular protection. In below-the-knee arteries, VC favours peripheral arterial occlusive disease and thus lower-limb amputation [6, 21]. Delaying lower-limb VC through the use of metformin might decrease the risk of amputation. This is of particular interest, since a recent analysis of the UK QResearch database suggested that metformin monotherapy reduces the risk of leg amputation relative to sulfonylureas or insulin monotherapy .
By demonstrating an inverse relationship between metformin use and VC in patients with type 2 diabetes, our results are in line with recent in vitro and in vivo data demonstrating that metformin can inhibit VC. At present, this effect is thought to be related to AMPK activation [18–20]. Indeed, it was recently suggested that AMPKα1 activation phosphorylates STAT-1, promotes Runx2 proteasome degradation and thus decreases the differentiation of VSMCs into calcifying cells . The AMPK1-related decrease in oxidative stress in endothelial cells may also reflect relevant protection against VC, since hydrogen peroxide is known to promote phenotypic switching of VSMCs by activating RUNX2 . In vitro, metformin’s AMPK phosphorylation reduces endothelial cells’ production of IL-6, a known inducer of VC . Metformin treatment of patients with polycystic ovary syndrome is associated with lower serum IL-6 levels . This was also the case in the present study, suggesting that IL-6 serum concentration reflects activation of AMPK by metformin. However, the fact that the association between metformin use and lower peripheral calcification was independent of IL-6 levels indicates that this was not the main mechanism.
We also found that metformin-treated patients had a higher eGFR-MDRD and were younger, less likely to be taking insulin and to have neuropathy, when compared with metformin-free patients. Given that age and eGFR-MDRD were also correlated with calcification score, the two parameters might be confounding factors that explain the intergroup differences in the peripheral calcification score. However, the results of our adjusted multivariate analysis indicate that the inverse association between VC and metformin use is independent of age and eGFR-MDRD. It has now been clearly established that chronic kidney disease (CKD) accelerates VC . As severe CKD is currently a contraindication for metformin prescription (due to a risk of lactic acidosis), diabetic CKD may constitute a lost opportunity to delay VC. A potential protective effect of metformin against VC would be a further argument in favour of maintaining metformin use in patients with diabetic nephropathy, since the additional risk of lactic acidosis due to metformin remains a subject to debate [44, 45]. With a view to shedding light on this attractive prospect of metformin use in CKD, evaluation in large clinical trials is now needed.
The present study’s limitations include the cross sectional design, the relatively small number of non-metformin users, and the lack of data on metformin concentrations. A specific, prospective, randomized or case-controlled study might overcome these limitations. The present study’s strengths include its assessment of arterial calcification with a highly sensitive CT scan and ultrasonography, and a thorough analysis of the prescribed antidiabetic drugs.
In conclusion, our study of patients with type 2 diabetes and high cardiovascular risk demonstrated that among antidiabetic drugs, only metformin treatment is negatively and independently associated with the severity of lower-limb artery calcification. The negative association between metformin use and VC may contribute (at least in part) to the drug’s well-known vascular protective effect. Our findings suggest that metformin use may constitute the best currently available strategy for delaying VC in type 2 diabetes, and may reinforce the justification for its first-line prescription in type 2 diabetes. Outside the field of diabetes, metformin might be a potential treatment option for other patients at risk of developing VC, such as those with CKD. These promising observations require confirmation in prospective studies.
AMP-activated protein kinase
chronic kidney disease
estimated glomerular filtration rate
endothelial nitric oxide synthase
endothelial progenitor cell
glucagon like peptide-1
ultrasensitive C-reactive protein
vascular smooth muscle cell
AM wrote the manuscript and performed statistical analyses. OB and AH were the principal investigators of the DIACART clinical cohort. OB contributed to analysis and discussion and wrote the paper. SKa designed the study, contributed to analysis and wrote the paper. SKe; JES; and PC assessed the calcification scores in patients; SL; CEA; ATL; ZAM; JDL; RM reviewed and edited the manuscript. All authors read and approved the final manuscript.
We thank the University of Lausanne, the clinical staff at the Centre for Clinical Investigations at Paris-Est CIC-1421, the Diabetes and Cardiology Departments from the Assistance Publique-Hôpitaux de Paris Pitié-Salpêtrière Hospital, and the members of Unit INSERM-1088 for their participation in this project. We also thank David Fraser (Biotech Communication SARL, Ploudalmézeau, France) for editorial assistance.
The authors declare that they have no competing interests.
Availability of data and materials
The detailed datasets analyzed during the current study are available from Olivier Bourron, (the principal investigator of the DIACART study) on reasonable request.
Ethics approval and consent to participate
The study protocol was approved by the ethic committee named Comité de Protection des Personnes, “Ile de France VI”, Paris, France. Written, informed consent was obtained from each study participant.
Eli Lilly and Company funded the study but was not involved in designing the study or collecting or interpreting study data.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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