Arterial Structure and Function in Mild Primary Hyperparathyroidism Is Not Directly Related to Parathyroid Hormone, Calcium, or Vitamin D

Objective Elevated levels of calcium and parathyroid hormone (PTH), characteristics of primary hyperparathyroidism (PHPT), may be associated with cardiovascular morbidity and mortality in the general population. We evaluated the possible vascular effects of these risk factors in patients with mild PHPT by using standard methods and new imaging techniques. Design A prospective case-control study. Subjects and Methods Forty-eight patients with mild PHPT without any known cardiovascular risk factors were studied at baseline and at one year after parathyroidectomy (PTX) in comparison with 48 healthy age- and gender-matched controls. We measured biochemical variables, augmentation index (AIx), aortic pulse wave velocity (PWVao), radial (IMTrad) and common carotid artery (IMTcca) intima media thicknesses, and the grayscale median (IM-GSM) of the latter. Results No significant differences were observed between PHPT patients and controls at baseline for AIx (28.6±12.2 vs. 27.7±12.8%), IMTrad (0.271±0.060 vs. 0.255±0.053 mm), IMTcca (0.688±0.113 vs. 0.680±0.135 mm), or IM-GSM (82.3±17.2 vs. 86.5±15.3), while PWVao was slightly higher in patients (8.68±1.50 vs. 8.13±1.55, p<0.05). Systolic blood pressure (SBP), calcium, and PTH were higher in patients compared with controls, and decreased after PTX, while vitamin D was lower in patients and increased after PTX. While AIx, PWVao, IMTrad, and IMTcca were related to SBP, neither correlated to vitamin D levels. Only PWVao correlated weakly to plasma PTH (r = 0.29, p<0.01) and ionized calcium (r = 0.22, p<0.05) but showed no relation when age and SBP were adjusted for. Conclusion We found normal arterial function despite high calcium, PTH, and low vitamin D levels, in patients with mild PHPT without cardiovascular risk factors. The cardiovascular risk associated with low vitamin D and/or high PTH and calcium levels may be explained by their coupling to blood pressure and other risk factors rather than direct effects on arterial structure.


Introduction
Associations between high calcium and parathyroid hormone (PTH) as well as low 25-OH-D levels and cardiovascular risk have been reported in the general population [1,2,3,4]. Recently, elevated PTH levels have been found to predict cardiovascular mortality in patients with coronary disease [5], as well as in the general population [6]. However, other recent data indicate no association between low 25-OH-D levels and all-cause mortality in older men [7].
Primary hyperparathyroidism (PHPT) is characterized by elevated calcium levels, inappropriately increased PTH levels, and is often associated with vitamin D deficiency [8].
Thus, PHPT is a good model to determine the influence of these alterations on the vasculature.
An increased mortality rate has been noted in both unselected PHPT [9], as well as in mild PHPT [10]. However, the majority of previous studies on PHPT include patients with varying disease severity in combination with pre-existing cardiovascular risk factors, which may confound relationships. Nevertheless, it is still unclear whether vascular structure and function are affected in mild PHPT without cardiovascular risk factors [11].
Endothelial function and vasodilatation regulated by nitride oxide (NO) release is of importance in the early atherosclerotic process. Endothelial vasodilatory dysfunction has been described in patients with PHPT [12]. In studies of mild PHPT, the augmentation index (AIx), an indirect measure of the endothelial function and arterial stiffness, has been reported to be increased [13,14]. Increased pulse wave velocity (PWV ao ) has been found in PHPT patients with hypertension [15]; however, conflicting results are reported [16]. Carotid intima-media thickness (IMT cca ) measured by ultrasound is associated with a risk of myocardial infarction and stroke [17,18]. Alterations in carotid IMT cca have been reported in patients with mild PHPT [19,20]; however the results are somewhat conflicting [16,21]. Among PHPT patients with or without cardiovascular risk factors, IMT cca was found to be increased only in the group with risk factors [22]. Recently, echogenicity of the carotid intima media complex has been demonstrated to be related to cardiovascular risk factors [23], and the intima thickness of the radial artery (IMT rad ) has been shown to be increased in hypertension [24], but none of these indices have yet been studied in PHPT.
With mild PHPT without concomitant disease or known cardiovascular risk factors as a model, our aim was to determine the potential effects of PTH, calcium, and vitamin D on arterial structure and function. Thus, applying the as mentioned novel diagnostic techniques, we compared patients with age-and gender matched healthy controls, and evaluated the vascular effects of normalizing PTH, calcium, and vitamin D by parathyroidectomy (PTX).

Subjects
In a prospective, previously described [25,26], case-control study at the Karolinska University Hospital in Stockholm, 410 PHPT patients (319 women) accepted for PTX between January 2006 and November 2008 were consecutively evaluated for possible participation. Patients accepted for PTX were included in the current study if they fulfilled the following criteria: calcium ,3.0 mmol/L; no diagnosed hypertension, diabetes mellitus, or renal diseases; no medication affecting the cardiovascular system; no current smoking; BMI ,28; and age .18 and ,70 years. The majority of our patients had plasma calcium levels below 2.75 mmol/L, and only five patients had plasma calcium levels between 2.76-2.97 mmol/L at the time of inclusion. Fifty-three patients with mild PHPT were consecutively included in the study. Five of the 53 patients were excluded; one man due to later findings of familial hypocalciuric hypercalcaemia, one woman regretted her decision to undergo PTX, one man was excluded because of carotid image storage failure and finally, two men were excluded because of lipid lowering medication. The final population consisted of 48 patients (13 men and 35 women). Of these, 13 PHPT patients had a history of kidney stones (n = 9) and/or osteoporosis (n = 6); while the remaining 35 patients had no classical symptoms coupled to PHPT, 22 of whom were diagnosed with PHPT at a routine health check-up, and the others sought medical attention because of fatigue or diffuse symptoms.
A healthy control group, age-and gender-matched, was randomly selected from the population registry of the city of Stockholm. They were informed by mail and asked to participate in the study. If they fulfilled the inclusion criteria, described above, they were included in the study. If anyone declined, a new randomly chosen control from the population registry was contacted. Two controls were replaced before entering the study: one because of hypertension and the other because of a high PTH level. The median (25, 75 percentiles) time from baseline to followup was 1.06 and 1.48 years. One woman did not participate in the vascular examinations at follow-up. The blood pressure and all examinations were performed the morning after an over-night fast, with a resting period of 30-60 minutes in supine position. The same investigator performed the ultrasound examinations and pulse wave analysis. Each participant provided written consent to participate in the study, which was approved by the Local Ethics Committee, Regional Ethical Review Board, EPN, of Stockholm, Sweden.

Blood Pressure, Body Mass Index
Blood pressure (BP) was measured in both arms using a digital automatic blood pressure monitor Omron M7 (Omron Healthcare Co., LTD, Kyoto, Japan). The mean values of systolic and diastolic blood pressure (SBP and DBP) in both arms were calculated. Mean arterial blood pressure (MAP) was calculated as DBP + (SBP-DPB)/3. Body mass index (BMI) was calculated by dividing weight (kg) by the square of height (m 2 ). Body surface area (BSA) was calculated by the formula: BSA (m 2 ) = 0.007184 6 (weight, kg) 0.425 6 (height, cm) 0.725 .

Augmentation Index and Pulse Wave Velocity
Augmentation index (AIx) and aortic pulse wave velocity (PWV ao ) were noninvasively measured using SphygmoCor equipment connected to a computer with SphygmoCor 2000 software (version 7.01, AtCor Medical, Sydney, Australia). Recordings were performed using a single high-fidelity tonometer gently pressed to the radial, carotid, and femoral arteries (SPT-301B, Millar Instruments, Houston, Texas, USA). To measure AIx, the radial artery waves were recorded and processed by the system software. The corresponding aortic pressure waveform was generated from an averaged radial artery waveform using a validated transfer factor [27,28]. AIx is defined as the difference between the first and the second peaks of the central aortic waveform, expressed as a percentage of the pulse pressure [29,30]. To obtain PWV ao , the pulse waveform was collected sequentially from femoral and carotid artery sites, and by using the R-wave (of a simultaneously recorded electrocardiography, ECG) as a reference, the mean difference in time (DT) between sites A (carotid) and B (femoral) was calculated. The surface distance (x subtracted ) was measured as (carotid-jugulum distance) subtracted from (jugulum-femoral distance). The direct distance over the body surface (x direct ) was obtained by a standardized formula: x direct = 0.45x subtracted +0.21* height +0.08 (m) [31]. The use of x direct leads to an overestimation of the real PWV ao, and a scaling factor was used to convert PWV ao distance to ''real'' PWV ao. The real PWV ao was calculated as: 0.8* x direct /DT, m/s, [32,33,34]. The brachial artery blood pressure was measured in connection with the examination, as a mean value of two measurements, by using an automatic monitor Omron M7 (Omron Healthcare Co., LTD., Kyoto, Japan. The radial and aortic blood pressure was calibrated against the brachial artery blood pressure. The aortic AIx and PWV ao are presented as mean values from two recordings.

Carotid Artery Ultrasound
Two-dimensional images of the common carotid artery (CCA) were acquired using an 8 MHz transducer, 7L, Vivid 7 (General Electric Company, Horten, Norway). The CCA was evaluated 1-2 cm proximal to the carotid bulb. Diastolic images at the time of the electrocardiographic R-wave were stored digitally on Echo-PAC (Image Vault 5.0 system, General Electric Company, Horten, Norway). For detection of IMT cca and IM-GSM, six digitized images were imported to validated automated software, Artery Measurement Software (AMS) [35,36]. AMS was developed in collaboration between the Department of Signals and Systems at Chalmers University of Technology, and the Physiology group at the Wallenberg Laboratory (www.wlab.gu.se), Gothenburg University, Gothenburg, Sweden. A region of interest (ROI) of a 10 mm long segment was manually placed proximal to the carotid bulb, Figure 1, upper panel. The boarders of the IMT cca of the far wall and the inner lumen diameter (LD cca ) were identified automatically by the program and the analysis could be manually corrected if necessary. IMT cca was defined as the distance from the leading edge of the lumen-intima interface to the leading edge of the media-adventitia of the far wall. LD cca was defined as the distance from the leading edge of the intima-lumen interface of the near wall and the leading edge of the lumen-intima interface of the far wall [37].
The IM-GSM was calculated in the same intima-media segment of the far wall that was evaluated for IMT cca , and from analysis of pixels on a scale from 0 (black) to 255 (white). The adventitia was used as the reference for white and the blood as the reference for black. IMT cca , IM-GSM, and LD cca are presented as mean values of six images from both the right and left CCA. Lumen diameter and IMT cca values are shown in mm, while IM-GSM is shown as median gray. At the end of the study, the same investigator performed the image analyses and calculations in random order. Intra-and interobserver variability was measured in 30 randomly selected participants, and the calculations in terms of coefficients of variation (CV) were: 2.90% and 3.80% for IMT cca, 0.40% and 0.70% for LD cca , and 2.74% and 3.81% for IM-GSM. Bland-Altman plots for IMT cca and IM-GSM are shown in Figure 2.

High-resolution Ultrasound
A high-resolution ultrasound investigation of the radial artery was performed in 43 patients. The images of the intima media of the radial artery were obtained by high-resolution ultrasound using a 55 MHz transducer (Vevo 770, VisualSonics, Toronto, Canada). B-mode images were recorded from the right radial artery in a longitudinal projection, 1-2 cm proximal to the fold separating the palm of the hand from the forearm. All cine-loops were stored on an external disk and measured offline using VisualSonics software. The thickness of the radial artery intima media (IMT rad ) and lumen diameter (LD rad ) were measured according to the leading edge principle [37]. Three sets of measurements were performed from each of the three representative images. The IMT rad of the far wall is presented as a mean value from nine measurements corresponding to the end-diastole, the smallest lumen diameter. The IMT rad was defined as the distance from the lumen-intima interface to the media-adventitia interface, Figure 1, lower panel. Diastolic LD rad was measured from the M-mode image, defined by the distance between the intima-lumen interface of the near wall and the lumen-intima interface of the far wall. LD rad is presented as a mean value taken from three representative beats. Intra-and interobserver variability in terms of CV were 5.78 and 10.94% for IMT rad , and 3.16 and 3.56% for LD rad .

Biochemical Variables
Plasma concentrations of total calcium, creatinine, glucose, high sensitivity C-reactive protein (hsCRP), phosphate, serum concentration of total cholesterol, triglycerides (TG), apolipoprotein A-1 (Apo-A1), and apolipoprotein B (Apo-B) were estimated using Synchron LXH 20 system (Beckman Coulter Inc., Brea, CA, USA). Serum-ionized calcium (Ca ++ ) was analyzed on ABL 800 (Radiometer, Copenhagen, Denmark), and plasma concentration of intact parathyroid hormone (PTH) was measured with electrochemiluminescence immunoassay on the Modular E system (Roche Diagnostics GmbH, Mannheim, Germany). Total serum IGF-1 was analyzed by chemiluminescence immunoassay on DPC Immulite 2000 (Siemens Healthcare Diagnostics, Munich, Ger-many). Serum concentrations of 25-OH-D were measured by chemiluminiscence on LiasonH (DiaSorin, S.p.A, Italy). The plasma concentrations of VWF antigen were determined with latex immunoassay on the BCS XP system (Siemens Healthcare Diagnostics, Munich, Germany). The plasma activity of PAI-1 was measured by a functional enzymatic ELISA assay (Chromolyze PAI-1) from Medinor (Axis-Shield, Dundee, U.K.). The samples of 25 hydroxyvitamin D (25-OH-D), von Willebrand factor (VWF) antigen, and PAI-1 were frozen at 270uC and analyzed in the same series in order to minimize inter-assay variation. Renal function was estimated by calculating the glomerular filtration rate (GFR) according to Cockroft-Gault's formula: GFR = (140-age in yr) x (weight in kg/creatinine) x (1.23 in men or 1.04 in women).
Vitamin D deficiency was defined as 25-OH-D below 50 nmol/ L.

Statistics
Statistical analyses were performed with PASW Statistics v18 (PASW Inc., Chicago, Illinois, U.S.A.). Data are expressed as mean 6 SD. Comparisons between the patients at baseline and the control group were performed with the Mann-Whitney U test for unpaired data, and for intra-individual analyses, Wilcoxon signed rank sum test was used. Spearmans rank correlation coefficients were computed to assess relationships between variables. Univariate and stepwise multiple linear regression analyses were used to evaluate relationships and adjust for confounders. Results from the multiple regression analyses were presented as standardized beta and adjusted R 2 .
The coefficient of variation (CV), defined as the standard deviation of the absolute differences between the measurements, divided by the mean of two measurements was used to evaluate the intra-and interobserver variability. The reproducibility was illustrated according to Bland-Altman [38]. All tests were twotailed and p,0.05 was considered to be statistically significant.

Clinical Data
Clinical data of healthy controls as well as PHPT patients at baseline and follow-up are presented in Table 1. The patients mean age at baseline was 5468.9 years (range 33 to 68 years). Fifteen patients were below 50 years of age. Forty-five patients had a single parathyroid adenoma, and three had multiglandular disease; median weight of removed tissue 409 mg. Heart rate and diastolic blood pressure did not differ, while systolic blood pressure was slightly higher in patients (p,0.05).

Biochemical Data
Biochemical data are presented in Table 2. Calcium and PTH levels were significantly higher and phosphate levels were lower in patients compared with controls and normalized after PTX. The vitamin D levels increased after surgery, but 19 out of 48 patients (40%) had a 25-OH-D level below 50 nmol/l at follow-up, 1564 months after PTX. There were no significant differences between the subgroups with 25-OH-D levels ,50 nmol/L, and .50 nmol/L, regarding SBP, AIx, PWV ao , IMT cca, IMT rad , IM-GSM, S-Ca, ionized Ca, or PTH levels. Further, these measures did not differ between those with 25-OH-D levels below or above the median (39 nmol/L).

Vascular Data
Vascular structural and functional results are presented in Table 3. We found no differences between patients and controls regarding AIx, estimated aortic blood pressure, IMT cca , IM-GSM values, or lumen of the CCA and no changes were observed during follow-up. PWV ao was slightly higher in patients 8.6861.50 (mean6SD) compared to controls 8.1361.55 (mean6SD), p,0.05, (range 6.6-13.2 for patients and 5.3-13.3 for controls), and did not change during follow-up. The IMT rad did not differ between the groups and remained unchanged at follow-up, while the LD rad was similar to that of controls; however, a marginal increase was noted after one year (p,0.05).

Correlations
We evaluated the univariate relations of vascular measures in terms of AIx, PWV ao, IMT rad , IMT cca , and IM-GSM to baseline data in the complete study cohort of patients and controls in order to verify expected patterns, Table 4. As noted, all vascular data except IM-GSM were related to age and systolic blood pressure. Further, correlations of AIx, PWV ao , IMT cca , IMT rad , and IM-GSM with biochemical variables are also presented in Table 4. Vascular function was not related to vitamin D. AIx and PWV ao were weakly related to cholesterol, PWV ao , and IM-GSM also to PTH, and PWV ao to ionized Ca and triglycerides. None of AIx, PWV ao , IMT rad , IMT cca, or IM-GSM correlated to P-Phosphate, hsCRP, Apo-B/Apo-A1, Ca*P product, or homocysteine levels.

Stepwise Regression Analyses
Multiple stepwise regression analyses with indices of vascular function (AIx, PWV ao , IMT cca, IMT rad and IM-GSM, one at a time) as dependent variables and demographic data (age, gender, SBP, height, and weight) as independent variables are presented in Table 5. More than 30% of the variation in AIx, PWV ao , and IMT cca, were explained by age and SBP, in AIx also by gender.
We also analyzed the possible influence of the disease-specific biochemical disturbances (PTH, ionized Ca, phosphate, 25-OH-D) on the five indices of vascular function, one at a time, considering also demographic data, Table 6. Apart from a weak relation between AIx and phosphate, no vascular measure was related to the biochemical variables.

Discussion
In this prospective case-control study of mild PHPT without any known cardiovascular risk factors or medications affecting the cardiovascular system, we found no indication that circulating levels of vitamin D influenced arterial structure or function. Wall composition (IM-GSM) and aortic stiffness (PWV ao ) were weakly related to PTH and the latter also to ionized calcium levels in univariate analysis, but not when adjusting for confounders like blood pressure. Furthermore, the PTX did not cause any change in indices of vascular function or arterial wall thickness. Our conclusions were substantiated by adding new variables, such as echogenicity of the carotid artery and intima media thickness of the radial artery to the established measures AIx, PWV ao , and IMT cca .
Thus, although vitamin D deficiency is common in patients with PHPT [8], and is associated with cardiovascular disease in the general population [39], we did not observe any relations between 25-OH-D and AIx, PWV ao , IMT rad , IMT cca , or IM-GSM in our study. Neither were these measures related to other biochemical data specifically abnormal in PHPT, such as Ca ++ and phosphate, apart from a correlation between PWV ao and PTH and ionized Ca and an inverse correlation between IM-GSM and PTH. Interestingly, Reis et al. found no association between vitamin D and carotid IMT apart from a weak association of 25-OH-D levels to internal carotid IMT when adjusting for, but not excluding, hypertension. Further, they found no evidence of an association between 1,25(OH) 2 D and common carotid IMT or internal carotid IMT, apart from a weak association to internal carotid IMT among patients with hypertension in one of several subgroup analyses [40]. The higher blood pressure among PHPT patients is not clearly understood. Despite the fact that we excluded patients with hypertension, we found significantly higher SBP, although within normal range, in patients compared with controls. SBP decreased after PTX in our patients, while it did not in another series of mild PHPT patients [41]. We have previously reported a weak but significant correlation between SBP and Ca++ as well as PTH levels when including both patients and controls [26]. It has been reported that vitamin D may influence blood pressure through the renin-angiotensin system [42], and a number of possible pathophysiological links to atherosclerosis have been ascribed to vitamin D deficiency, including activation of the renin angiotensin system [43]. Our data add strength to the hypothesis that associations between the atherosclerotic process and circulating levels of vitamin D, ionized Ca, and PTH are mediated through blood pressure and other risk factors. With regard to the Table 3. Augmentation index and ultrasound measurements for healthy controls and patients with mild primary hyperparathyroidism before and after parathyroidectomy.  relation between vitamin D status and cardiovascular risk, many issues still remain to be resolved. Recent comprehensive reviews do not support a strong link between vitamin D status or supplementation and cardiometabolic outcome or cardiovascular events [44,45], and another systematic review and meta-analysis, based on 51 trials, found no significant correlation between vitamin D status, hypertension, or cardiovascular mortality [46]. Interestingly, it was recently demonstrated that PHPT causes up-regulation of the matrix metallopeptidase 9 (MMP9) gene and a number of other inflammatory and metabolic genes in fat tissue, with possible impacts on blood pressure and atherosclerosis [47]. In our study of normotensive PHPT patients and controls, we found slightly higher blood pressure and PWV ao in patients. However, data are not unanimous. While Rosa et al. noted PHPT patients to have increased arterial stiffness with and without hypertension [48], Kosch et al. showed no difference in PWV between PHPT patients and controls, and found no correlations between PWV and increased PTH levels [16].
Our PHPT patients and healthy controls showed no difference in AIx. This is in contrast to the results of Smith et al. [13] and Rubin et al. [14], who also studied patients with mild PHPT. Smith et al. [13] reported higher AIx in patients with mild PHPT compared to controls, and Rubin et al. [14] asserted that PHPT was independently associated with increased AIx. In contrast to Rubin et al. [14], we did not find any correlation between AIx and elevated PTH. A plausible explanation for the discrepancy is that Rubin et al. [14] studied groups containing PHPT patients with hypertension and patients on cardiovascular medication. The association between the severity of PHPT and cardiovascular risk factors, however, is not universal. Similar amount of risk factors was recently reported in hypercalcemic and normocalcemic PHPT patients although cardiovascular and cerebrovascular diseases were more common in hypercalcemic PHPT [49]. In the same study, however, vascular stiffness was not higher in this group than in normocalcemic PHPT or controls, and in congruence with our material unrelated to calcium and PTH.
Probably, cardiovascular diseases combined with PHPT are more likely to affect the arterial wall and IMT than PHPT alone. This is supported by Fallo et al. [22], who included PHPT patients with and without cardiovascular risk factors. When compared to healthy controls, only PHPT patients with concomitant cardiovascular risk factors were found to have an increased IMT of the carotid artery wall. Similarly Walker et al. [20] reported increased carotid IMT in PHPT patients, including those with cardiovascular diseases, compared to controls. Nuzzo et al. [19] excluded subjects with high blood pressure or clinical cardiovascular disease and still found significantly higher carotid IMT values in 20 selected patients compared with controls. However, the authors did not indicate the lipid levels in their study group. Kosch et al. [16] found no disturbance in brachial and carotid IMT or aortic PWV in PHPT patients compared to controls, and Lumachi et al. [21] reports no improvement in carotid IMT after 18 months of PTX follow-up; further, no correlations between serum calcium and IMT was found. In our study, with careful exclusion of   patients with cardiovascular risk factors, we did not observe any differences between patients and controls at baseline, apart from slightly higher SBP and PWV ao in patients with a significant reduction in blood pressure one year after PTX. All our vascular measurements, apart from IM-GSM, were related to age and blood pressure. Adjusting for age and blood pressure, PWV ao was not related to circulating levels of PTH, Ca ++ , phosphate, or 25-OH-D.
In order to investigate the vascular structure more thoroughly, we have used new validated techniques in our study, such as grayscale median for the evaluation of echogenicity of the carotid intima media, and a high-resolution ultrasound for measurement of IMT in the radial artery. We have demonstrated that highresolution ultrasound allows measurement of very thin structures such as IMT of the rat carotid artery wall [50], and it has also been shown that measurement of the human radial artery IMT is feasible by this technique [24]. In the current study, we measured the intima media thickness in the radial artery and found no significant increase in IMT rad in the PHPT patients compared with controls. By measurement of the grayscale in the intima media images of carotid artery, we tried to obtain information regarding the wall composition, with the assumption that fibrotic infiltration should be more echogenic and lipidous transformation should be more echolucent. Earlier studies have shown that IM-GSM in CCA is closely related to the echogenicity in overt carotid plaques; moreover, the same group further reported a relationship between echolucency in the intima-media complex and cardiovascular risk factors in elderly subjects [23,51]. However, our study did not indicate abnormal composition of the carotid artery wall as evaluated by this technique.

Strengths and Limitations
To our knowledge, this is the first study to describe IMT rad and the echogenicity in the intima media of the CCA in patients with mild PHPT. The strict design, excluding cardiovascular risk factors, is the strength of our study, which should favorably influence the reliability of our results. The material is comparatively large for this type of study; however, it is too small for any prognostic evaluations.
We measured the IMT of the common carotid artery in the far wall only, as we assumed relatively symmetrical wall thickness in our patients and controls. Since most patients with PHPT today do not express typical signs and since calcium-and PTH-levels are not examined routinely, it is rarely possible to estimate the duration of the disease.

Conclusion
We found normal arterial function, despite high PTH and Ca as well as low vitamin D levels, in patients with mild PHPT without cardiovascular risk factors. The cardiovascular risk associated with low vitamin D and/or high PTH and Ca levels may be explained by their coupling to blood pressure and other risk factors rather than direct effects on the arterial structure. Our findings support the importance of adequate blood pressure control in PHPT if PTX is not performed, but do not indicate vascular abnormalities motivating extended follow-up after PTX. Table 6. Stepwise regression analyses with indices of vascular function as dependent variables, and demographic and biochemical data as independent variables in the whole group of PHPT patients and controls.