Skip to main content

Advertisement

Association of C2, a derivative of the radial artery pressure waveform, with new onset of type 2 diabetes mellitus: the MESA study

Article metrics

Abstract

Background

Although microvascular dysfunction is known to result from diabetes, it might also lead to diabetes. Lower values of C2, a derivative of the radial artery pressure waveform, indicate microvascular dysfunction and predict hypertension and cardiovascular disease (CVD). We studied the association of C2 with incident diabetes in subjects free of overt CVD.

Methods

Among multi-ethnic participants (n = 5214), aged 45–84 years with no diabetes, C2 was derived from the radial artery pressure waveform. Incident diabetes (N = 651) was diagnosed as new fasting glucose ≥ 126 mg/dL or antidiabetic medicine over ~ 10 years. The relative incidence density (RID) for incident diabetes per standard deviation (SD) of C2 was studied during ~ 10 years follow-up using four levels of adjustment.

Results

Mean C2 at baseline was 4.58 ± 2.85 mL/mmHg × 100. The RID for incident diabetes per SD of C2 was 0.90 (95% CI 0.82–0.99, P = 0.03). After adjustment for demographics plus body size, the corresponding RID was 0.81 (95% CI 0.73–0.89, P < 0.0001); body mass index (BMI) was the dominant covariate here. After adjustment for demographics plus cardiovascular risk factors, the RID was 0.98 (95% CI 0.89, 1.07, P = 0.63). After adjustment for all the parameters in the previous models, the RID was 0.87 (95% CI 0.78, 0.96, P = 0.006).

Conclusions

In a multi-ethnic sample free of overt CVD and diabetes at baseline, C2 predicted incident diabetes after adjustment for demographics, BMI and CVD risk factors. Differences in arterial blood pressure wave morphology may indicate a long-term risk trajectory for diabetes, independently of body size and the classical risk factors.

Background

A large part of the pathogenesis in diabetes has been focused on insulin resistance and inflammation. Microvascular disease resulting from diabetes has been described as leading to diabetic retinopathy, nephropathy, and cardiomyopathy. For example Kannenkeril et al. [1] found microvascular changes in the retinal, renal, and systemic circulation in type 2 diabetes patients. Tuttolomundo et al. [2] similar found changes in arterial stiffness in diabetic foot syndrome. Benitez-Aguirre et al. [3] found that studied greater arterial stiffness was associated with later microvascular complications in type 1 diabetes patients. During the last years it has been hypothesized that microvascular dysfunction might also be a precursor of development of diabetes, independently of impaired fasting glucose [4, 5]. Microvascular dysfunction may occur as a consequence of endothelial dysfunction. Biomarkers of endothelial dysfunction were associated with a greater risk for diabetes [6,7,8,9,10,11,12,13]. A few studies demonstrated a higher incidence of type 2 diabetes with smaller baseline retinal arteriolar diameter and arteriolo–venular ratio (AVR), while venular diameters were not significantly associated with incident diabetes [14,15,16,17]. In addition, an attenuated endothelium-dependent vasoreactivity response was significantly associated with incident diabetes in patients with hypertension [18].

Measurement of arterial stiffness is of scientific interest because it is a phenotype that is an early marker for cardiovascular disease and is simple to implement clinically. It could also predict new onset diabetes, but the latter is still to be proven. During the last 2 decades, a derivative of the continuous radial artery blood pressure waveform, C2 which has been designated as either distal arterial compliance or small artery elasticity has been studied in the Multi-Ethnic Study of Atherosclerosis (MESA) [19,20,21]. In MESA, C2 predicted new onset of arterial hypertension, cardiovascular disease (myocardial infarction, coronary artery disease, stroke, heart failure, peripheral artery disease) and decline in renal function beyond the classical risk factors and inflammatory parameters [19,20,21]. There is evidence that C2 may be considered as a marker for endothelial function/microvascular function [22]. Therefore we hypothesized that C2 may be a predictor for future development of diabetes.

Methods

Study cohort

The MESA is a multi-center, prospective cohort designed to investigate prevalence, correlates, and progression of subclinical (asymptomatic) atherosclerosis and their associations with incident clinical events. A detailed description of the study design, recruitment methods, and examination components and data collections has been published [23]. In brief, participants included 6814 men and women (age 45–84) of Caucasian, Hispanic, African–American and Chinese descent, free from clinically manifest CVD at baseline. Signed informed consent was obtained for all participants, and institutional review board approval was obtained for all participating institutions. We included 5214 participants free of diabetes and who had a C2 measurement at baseline and any follow-up visit at which a diagnosis of diabetes could be made.

C2 measurement

At the baseline visit between 2000 and 2002, arterial waveforms were recorded for the entire cohort using the HDI/PulseWave CR-2000 (Hypertension Diagnostics, Inc., Eagan, Minnesota). Details of this procedure have previously been published [24]. In brief, a solid state pressure transducer array (tonometer) was placed over the radial artery of the dominant arm to record the pulse contour. C2 is estimated by the device from the waveform modeled as a sinusoidal function dampened by a decaying exponential. An index estimated directly from the waveform is divided by systemic vascular resistance (SVR) to obtain C2. SVR is estimated as mean arterial blood pressure/cardiac output, and cardiac output is estimated from ejection time taken from the pulse waveform, heart rate, age, height. Higher C2 is considered to represent a more favorable cardiovascular status.

Risk factor assessment

Participants were given standardized questionnaires at baseline, which were used to obtain information on demographics, medical history, and smoking history. A medication inventory was also performed, and medications were grouped based on use to treat high blood pressure, or elevated blood glucose. Height and weight were assessed using a standardized protocol and body mass index (BMI) was defined (kg/m2). Blood pressure was measured three times in the seated position with an automated oscillometric sphygmomanometer after at least 5 min of rest. The average of the last 2 measurements was used. Standard measurements were taken for height and weight, and venous blood samples were obtained after a 12 h fast for measurements of total cholesterol, high-density lipoprotein (HDL) cholesterol, triglycerides and glucose. Physical activity (min/week in sports and dance) and TV watching (min/week) was assessed by a questionnaire.

Study endpoint: diabetes mellitus type 2

Among those free of diabetes at baseline according to self-reported clinical statement, baseline fasting plasma glucose < 126 mg/dL and no use of anti-diabetic medications at baseline, incident diabetes was defined as fasting plasma glucose ≥ 126 mg/dL or start of anti-diabetic medications during the consecutive MESA follow-up visits. Note that it was not possible to distinguish incident type 1 from type 2 diabetes, but at MESA ages most diabetes would be type 2. Diabetes was identifiable only at clinic visits, which occurred at mean 1.64 years after baseline in 97.5% of participants, 3.20 years in 93.5%, 4.84 years in 91.3% and 9.47 years in 75.6% of participants.

Statistical analysis

Descriptive statistics for the study cohort were summarized by means (SD) and ranges for continuous variables, and frequencies for categorical variables following five C2 categories with equal intervals, but open-ended extremes (Table 1). Over a median follow-up of approximately 10 years, we computed the relative incidence density for new onset diabetes per standard deviation of C2 as a continuous variable and separately for each C2 category using Poisson regression using 4 levels of adjustment: model 1 adjusted for age, race, sex; model 2 based on model 1 with further adjustment for body size (BMI and height; note that although height is part of the mathematical definition of BMI, BMI and height are uncorrelated); model 3 based on model 1 with further adjustment for risk factors (heart rate, blood pressure and antihypertensive therapy, blood lipids and cholesterol lowering therapy, smoking, and physical activity); and model 4 including all of the above variables. The analysis of C2 categories was also represented graphically. The study participants with borderline diabetes are at much higher risk for incident diabetes; this may differentially influence diabetes risk by C2 status. We therefore also examined the interaction with baseline impaired fasting glucose status and C2 in prediction of new onset diabetes. Because C2 correlates with BMI, we calculated the Pearson correlations (sex-adjusted) with BMI at baseline. In a subset analysis, we also calculated the Pearson correlations (sex-adjusted) with different contributing parameters to BMI, which were visceral fat (VAT), abdominal intermuscular adipose tissue (IMAT) and muscle lean volumes (LEAN). The latter measurements were obtained in a subset of participants by computed tomography at MESA exams 2 or 3 (means 1.64 and 3.20 years after MESA baseline, respectively) [25].

Table 1 Participant characteristics following five C2 categories (with equal intervals with open-ended extremes) in the Multi-Ethnic Study of Atherosclerosis, 2000–2002

We considered P < 0.05 to be noteworthy in general screening of findings. Analyses were performed using PC-SAS, version 9.4 (SAS Institute, Cary, NC).

Results

Table 1 summarizes the characteristics of the study participants following C2 categories. Mean C2 at baseline was 4.58 ± 2.85 mL/mm Hg × 100. C2 was lower with a higher age. Females had lower C2 than males. Height was associated with higher C2. Participants with a lower C2 had higher systolic and diastolic blood pressure and they received more antihypertensive therapy. Participants with lower C2 had a more sedentary lifestyle. Study participants with a higher C2 tended to have higher BMI.

Incident DM occurred in 651 participants during approximately 10 years follow-up. In Table 2, after adjustment for demographics, the relative incidence density (RID) for incident DM per standard deviation of C2 was 0.90 (95% CI 0.82–0.99, P = 0.03). After additional adjustment beyond demographics for body size (namely, BMI and height) the corresponding RID was 0.81 (95% CI 0.73–0.89, P < 0.0001); BMI was the dominant covariate in model 2. Omission of height from the model had little effect on the solution (data not shown). After adjustment for cardiovascular risk factors beyond demographics, the RID for incidence of DM for C2 was 0.98 (95% CI 0.89, 1.07, P = 0.63). In model 4 in which there was an adjustment for demographics, BMI, height and CV risk factors the RID for DM was 0.87 (95% CI 0.78, 0.96, P = 0.0.006). Figure 1 illustrates the incidence of DM by categories of C2. Whereas adjustment for CV risk factors tended to attenuate the association of C2 with incident diabetes (model 3), the strongest inverse association of C2 with incident diabetes occurred in model 2, adjusting for demographics, BMI and height; the association in model 2 is accentuated compared to the one in model 1 with adjustment for demographics alone. There was no significant interaction between impaired fasting glucose status and C2 in prediction of incident diabetes (P = 0.99). No race/ethnicity interaction with C2 was observed (data not shown).

Table 2 Relative incidence density (RID) diabetes per standard deviation of C2 over approximately 10 years of follow-up
Fig. 1
figure1

Incident diabetes by categories of C2 at 4 levels of adjustment. Adjustment for body size (BMI and height) accentuated the association of C2 with diabetes, while adjustment for cardiovascular risk factors attenuated the association. BMI body mass index, risk factors: heart rate, blood pressure and antihypertensive therapy, blood lipids and cholesterol lowering therapy, smoking, physical activity

In a subset of 1629 participants (Table 3) in whom IMAT, LEAN, and VAT were assessed at exams 2 or 3, although C2 at exam 1 was positively correlated with BMI. C2 was positively associated with muscle LEAN assessed 2–4 years later. BMI, IMAT and VAT form a triad with pairwise correlations of 0.57–0.61, P < 0.0001, but it is of note that although IMAT and LEAN have an inverse correlation (r = − 0.21, P < 0.0001), BMI and LEAN have a positive correlation (r = 0.29, P < 0.0001).

Table 3 Pearson correlations (sex-adjusted) in 1629 participants among C2 and several measures of body mass index (BMI, at baseline = exam 1) and abdominal intermuscular adipose tissue (IMAT), muscle lean volume (LEAN) and visceral adipose tissue (VAT) obtained by computed tomography at MESA (mean 1.64 and 3.20 years after MESA baseline, respectively = exam 2 and 3)

Discussion

In a multi-ethnic sample free of overt CVD and diabetes at baseline, a higher C2 predicted significantly lower incident diabetes after adjustment for demographics, BMI and CVD risk factors. As such, changes in arterial blood pressure wave morphology may manifest a long-term risk trajectory for diabetes independently of demographics, body size and the classical risk factors. This finding is in agreement with a finding in the Malmö Diet and Cancer cardiovascular cohort, for another measure of arterial stiffness, increased carotid-femoral pulse wave velocity, which was associated with increased incidence of diabetes independent of other risk factors [26].

Among variables based on the pulse waveform, only C2 has been shown to be measure of the competence of the microcirculation [22]. Pulse wave velocity, which depends only on the arrival time of the waveform, is most studied. The assumption that connects pulse wave velocity to arterial stiffness is that a stiffer tube carries a pressure wave at higher velocity than a flexible tube. However, smaller arteries are not considered in this assumption. Other measures do depend on the shape of the waveform. Reflection magnitude [27] is based on the idea that when a forward pressure wave travels through a stiff artery, a reflection wave is formed, and pressure reflects back towards the origin of the forward wave. The augmentation index is computed after applying a transfer function to approximate the central waveform. The augmentation index is the ratio of the second to the first peak in the central waveform. The second peak is thought to be higher in the presence of a reflection wave.

The measures C1 and C2 were initially derived from a third order Windkessel model of compliance in an electrical circuit. The model assumes two capacitors, and when the capacitances C1 * R and C2 * R are divided by the systemic resistance, R, two systemic compliance measures, C1 and C2, result. The link to arterial stiffness is less direct in this case then in the case of the previously discussed measures. The proprietary owners of C1 and C2 explored the solution to the Windkessel model and suggest that C1 strongly reflects the rapid decay of pressure during diastole, while C2 is a measure of the dampening oscillations as the waveform proceeds from late systole until mitral valve closure during diastole. The dampening of these oscillations could be the result of a superimposed reflection wave. C2 also has a microcirculatory dimension. Gilani et al. [22] measured C1 and C2 in 10 healthy volunteers (3 male and 7 female) before and after inhibiting dilation of the small vessels by intra-arterial infusion of the substituted arginine NG-nitro-l-arginine-methyl ester (l-NAME). C2 was decreased after inhibition, while C1 was not. The designation small artery elasticity for C2, which has been used by the proprietary owners of C2 and by us, may therefore be too specific. We prefer to use the more generic name C2, recognizing that C2 uniquely among waveform interpretations has been shown to relate to the microcirculation.

In our analyses, the association of C2 and incident diabetes is dominated among covariates by the association of C2 with BMI, in which those with more favorable C2 had a higher BMI (BMI is therefore a negative confounder for the association of C2 and incident diabetes) [28]. Although the physiologic basis for the positive association of C2 with BMI is not well understood, the situation may be complex [29]. Forbang et al. further discussed this anti-intuitive finding and confirmed that C2 was positively associated with BMI, but also that C2 was inversely related to visceral adipose tissue once muscle mass was considered [25]. Clearly, BMI does not discriminate well between peripheral and harmful fat. As shown in Table 3 of the present paper, this association with BMI may have as much to do with BMI as an indicator of lean muscle volume as with BMI as an indicator of body fatness. In any case, BMI is a factor which is well known to be associated with higher incidence of diabetes, and its paradoxical association with better C2 must be considered in evaluating the association of C2 with diabetes.

Given the known association of C2 with microvascular function [22], the association we found between a low C2 and incident diabetes could have resulted from pre-existing microvascular changes. While microvascular dysfunction may occur independently of dysglycemia, we acknowledge that the microvascular dysfunction represented by low C2 could be the result of dysglycemia even below the fasting glucose cutpoint for diabetes, although in our data baseline C2 and fasting glucose were only weakly correlated. Muris et al. found in their meta-analysis that microvascular dysfunction (assessed using a variety of modalities) was associated with 10 to 49% higher incidence of type 2 diabetes [5]. This finding is consonant with the 50% higher diabetes incidence density, comparing the lowest (least favorable) to highest (most favorable) C2 categories in Fig. 1 in our study.

Strength of our study includes a representation of multiple ethnicities, both genders and a relatively large sample size. Prevalent CVD at baseline was an exclusion criterion. Our study also has the limitation that diabetes could only be diagnosed at 4 time points over the approximate 10 year follow-up period, and some late-appearing diabetes diagnoses were missed, when diabetes onset was after the last attended clinic visit. Selective survival bias is also a possibility. The observational association between C2 and incidence DM cannot prove a causal relationship and residual confounding is a possibility. A possible advantage to use the radial artery waveform for the calculation of C2 is that the arterial waveform analysis can also be used by applying mathematical algorithms to calculate cardiac output non-invasively. A study by Maddali et al. [30] used radial and femoral artery waveforms to calculate cardiac output; this measure correlated well with echocardiographic cardiac output measurements.

Conclusions

Our study demonstrated that C2, which is a derivative from the arterial blood pressure wave morphology, predicts new onset of diabetes independently from the classical risk factors. C2 provides information about microvascular function and therefore these findings add important information in the pathogenesis of diabetes that microvascular dysfunction is an important contributor for new onset of type 2 diabetes. Future studies are warranted to examine the role of new classes of anti-diabetic drugs, which a have a beneficial effect on the microcirculation and small vessels, to prevent new development of type 2 diabetes.

Availability of data and materials

Data and materials are available upon request.

Abbreviations

AVR:

arteriolo–venular ratio

BMI:

body mass index

C2:

derivative of the radial artery pressure waveform

CI:

confidence interval

CVD:

cardiovascular disease

DM:

diabetes mellitus

IMAT:

abdominal intermuscular adipose tissue

LEAN:

muscle lean volumes

l-NAME:

arginine NG-nitro-l-arginine-methyl ester

MESA:

Multi-Ethnic Study of Atherosclerosis

RID:

relative incidence density

SD:

standard deviation

VAT:

visceral fat

References

  1. 1.

    Kannenkeril D, Bosch A, Harazny J, Karg M, Jung S, Ott C, et al. Early vascular parameters in the micro- and macrocirculation in type 2 diabetes. Cardiovasc Diabetol. 2018;17(1):128. https://doi.org/10.1186/s12933-018-0770-4.

  2. 2.

    Tuttolomondo A, Casuccio A, Guercio G, Maida C, Del Cuore A, Di Raimondo D, et al. Arterial stiffness, endothelial and cognitive function in subjects with type 2 diabetes in accordance with absence or presence of diabetic foot syndrome. Cardiovasc Diabetol. 2016;16(1):2. https://doi.org/10.1186/s12933-016-0483-5.

  3. 3.

    Benitez-Aguirre PZ, Januszewski AS, Cho YH, Craig ME, Jenkins AJ, Donaghue KC. Early changes of arterial elasticity in type 1 diabetes with microvascular complications—a cross-sectional study from childhood to adulthood. J Diabetes Complicat. 2017;31(12):1674–80.

  4. 4.

    Stehouwer CDA. Microvascular dysfunction and hyperglycemia: a vicious cycle with widespread consequences. Diabetes. 2018;67:1729–41.

  5. 5.

    Muris DMJ, Houben AJHM, Schram MT, Stehouwer CDA. Microvascular dysfunction is associated with a higher incidence of type 2 diabetes mellitus. A systemic review and meta-analysis. Arterioscler Thromb Vasc Biol. 2012;32:3082–94.

  6. 6.

    Duncan BB, Schmidt MI, Offenbacher S, Wu KK, Savage PJ, Heiss G. Factor VIII and other hemostasis variables are related to incident diabetes in adults: the Atherosclerosis Risk in Communities (ARIC) Study. Diabetes Care. 1999;22:767–72.

  7. 7.

    Meigs JB, O’donnell CJ, Tofler EJ, Benjamin CJ, Fox CS, Lipinska I, et al. Hemostatic markers of endothelial dysfunction and risk of incident type 2 diabetes: the Framingham Offspring Study. Diabetes. 2006;55:530–7.

  8. 8.

    Sattar N, Murray HM, Welsh P, Blauw GJ, Buckley BM, de Craen AJ, et al. Are elevated circulating intercellular adhesion molecule 1 levels more strongly predictive of diabetes than vascular risk? Outcome of a prospective study in the elderly. Diabetologia. 2009;52:235–9.

  9. 9.

    Wannamethee SG, Sattar N, Rumley A, Whincup PH, Lennon L, Lowe GD. Tissue plasminogen activator, von Willebrand factor, and risk of type 2 diabetes in older men. Diabetes Care. 2008;31:995–1000.

  10. 10.

    Meigs JB, Hu FB, Rifai N, Manson JE. Biomarkers of endothelial dysfunction and risk of type 2 diabetes mellitus. JAMA. 2004;291:1978–86.

  11. 11.

    Song Y, Manson JE, Tinker L, Rifai N, Cook NR, Hu FB, et al. Circulating levels of endothelial adhesion molecules and risk of diabetes in an ethnically diverse cohort of women. Diabetes. 2007;56:1898–904.

  12. 12.

    Hoogeveen RC, Ballantyne CM, Bang H, Heiss G, Duncan BB, Folsom AR, et al. Circulating oxidised low-density lipoprotein and intercellular adhesion molecule-1 and risk of type 2 diabetes mellitus: the Atherosclerosis Risk in Communities Study. Diabetologia. 2007;50:36–42.

  13. 13.

    Thorand B, Baumert J, Chambless L, Meisinger C, Kolb H, Döring A, et al. Elevated markers of endothelial dysfunction predict type 2 diabetes mellitus in middle-aged men and women from the general population. Arterioscler Thromb Vasc Biol. 2006;26:398–405.

  14. 14.

    Ikram MK, Janssen JA, Roos AM, Rietveld I, Witteman JC, Breteler MM, et al. Retinal vessel diameters and risk of impaired fasting glucose or diabetes: the Rotterdam study. Diabetes. 2006;55:506–10.

  15. 15.

    Kifley A, Wang JJ, Cugati S, Wong TY, Mitchell P. Retinal vascular caliber and the long-term risk of diabetes and impaired fasting glucose: the Blue Mountains Eye Study. Microcirculation. 2008;15:373–7.

  16. 16.

    Wong TY, Klein R, Sharrett AR, Schmidt MI, Pankow JS, Couper DJ, et al. Retinal arteriolar narrowing and risk of diabetes mellitus in middle-aged persons. JAMA. 2002;287:2528–33.

  17. 17.

    Wong TY, Shankar A, Klein R, Klein BE, Hubbard LD. Retinal arteriolar narrowing, hypertension, and subsequent risk of diabetes mellitus. Arch Intern Med. 2005;165:1060–5.

  18. 18.

    Perticone F, Maio R, Sciacqua A, Andreozzi F, Iemma G, Perticone M, et al. Endothelial dysfunction and C-reactive protein are risk factors for diabetes in essential hypertension. Diabetes. 2008;57:167–71.

  19. 19.

    Peralta CA, Adeney KL, Shlipak MG, Jacobs D Jr, Duprez D, Bluemke D, et al. Structural and functional vascular alterations and incident hypertension in normotensive adults: the Multi-Ethnic Study of Atherosclerosis. Am J Epidemiol. 2010;171:63–71.

  20. 20.

    Duprez DA, Jacobs DR Jr, Lutsey PL, Bluemke DA, Brumback LC, Polak JF, et al. Association of small artery elasticity with incident cardiovascular disease in older adults: the Multi-Ethnic Study of Atherosclerosis. Am J Epidemiol. 2011;174:528–36.

  21. 21.

    Peralta CA, Jacobs DR Jr, Katz R, Ix JH, Madero M, Duprez DA, et al. Association of pulse pressure, arterial elasticity, and and endothelial function with kidney function decline among adults with estimated GFR > 60 mL/min/1.73 m2: the Multi-Ethnic Study of Atherosclerosis (MESA). Am J Kidney Dis. 2012;59:41–9.

  22. 22.

    Gilani M, Kaiser DR, Bratteli CW, Alinder C, Rajala S, Bank AJ, et al. Role of nitric oxide deficiency and its detection as a risk factor in pre-hypertension. J Am Soc Hypertens. 2007;1:45–55.

  23. 23.

    Bild DE, Bluemke DA, Burke GL, Detrano R, Diez Roux AV, Folsom AR, et al. Multi-Ethnic Study of Atherosclerosis: objectives and design. Am J Epidemiol. 2002;156:871–81.

  24. 24.

    Finkelstein SM, Cohn JN. First- and third-order models for determining arterial compliance. J Hypertens Suppl. 1992;10(6):S11–4.

  25. 25.

    Forbang NI, Allison MA, Ix JH, Criqui MH, Vaidya D, Yeboah J, et al. Associations of body composition measures and C2, a marker for small artery elasticity: the MESA. Obesity. 2015;23:2294–8.

  26. 26.

    Muhammad IF, Borné Y, Östling G, Kennbäck C, Gottsäter M, Persson M, et al. Arterial stiffness and incidence of diabetes: a population-based cohort study. Diabetes Care. 2017;40:1739–45.

  27. 27.

    Chirinos JA, Kips JG, Jacobs DR Jr, Brumback L, Duprez DA, Kronmal R, Bluemke DA, Townsend RR, Vermeersch S, Segers P. Arterial wave reflections and incident cardiovascular events and heart failure: MESA (Multiethnic Study of Atherosclerosis). J Am Coll Cardiol. 2012;60(21):2170–7.

  28. 28.

    Duprez DA, Jacobs DR Jr, Lutsey PL, Herrington D, Prime D, Ouyang P, et al. Race/ethnic and sex differences in large and small artery elasticity—results of the multi-ethnic study of atherosclerosis (MESA). Ethn Dis. 2009;19:243–50.

  29. 29.

    Evans JM, Wang S, Greb C, Kostas V, Knapp CF, Zhang Q, et al. Body size predicts cardiac and vascular resistance effects on men’s and women’s blood pressure. Front Physiol. 2017;8:561.

  30. 30.

    Maddali MM, Waje ND, Sathiya PM. Authentication of radial versus femoral arterial pressure waveform-derived cardiac output with transesophageal echocardiography-derived cardiac output measurements in patients undergoing on-pump coronary bypass surgery. J Cardiothorac Vasc Anesth. 2017;31:1183–9.

Download references

Acknowledgements

Not applicable.

Funding

This research was supported by contracts HHSN268201500003I, N01-HC-95159, N01-HC-95160, N01-HC-95161, N01-HC-95162, N01-HC-95163, N01-HC-95164, N01-HC-95165, N01-HC-95166, N01-HC-95167, N01-HC-95168 and N01-HC-95169 from the National Heart, Lung, and Blood Institute, and by grants UL1-TR-000040, UL1-TR-001079, and UL1-TR-001420 from the National Center for Advancing Translational Sciences (NCATS). Drs. Jacobs and Duprez were also supported by a grant from the National Heart, Lung, and Blood Institute, R01 HL098382. The authors thank the other investigators, the staff, and the participants of the MESA study for their valuable contributions. A full list of participating MESA investigators and institutions can be found at http://www.mesa-nhlbi.org.

Author information

DAD and DRJ—study conception and design, data collection, drafting manuscript. DRJ—statistical analyses., drafting manuscript. NAF, MAA, CAP, SS—critical revisions to manuscript. All authors read and approved the final manuscript.

Correspondence to Daniel A. Duprez.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the Institutional Review Board of the six University MESA study centers and all participants consented to participating in this study.

Consent for publication

All study participants consented to participating in this study, and having their results published as part of this study.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This 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.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Duprez, D.A., Forbang, N.I., Allison, M.A. et al. Association of C2, a derivative of the radial artery pressure waveform, with new onset of type 2 diabetes mellitus: the MESA study. Cardiovasc Diabetol 18, 62 (2019) doi:10.1186/s12933-019-0868-3

Download citation

Keywords

  • Arterial pressure waveform
  • C2
  • Incident diabetes type 2
  • Cohort study
  • Cardiovascular risk factors