Neurovascular Compression in Arterial Hypertension: Correlation of Clinical Data to 3D-Visualizations of MRI-Findings

Panagiota Manava1, 5, *, Peter Hastreiter1, Roland E. Schmieder2, Susanne Jung2, Rudolf Fahlbusch1, 4, Arnd Dörfler3, Michael M. Lell5, 7, Michael Buchfelder1, Ramin Naraghi1, 6
1 Department of Neurosurgery, Friedrich-Alexander University, Erlangen-Nuremberg (FAU), Erlangen
2 Department of Nephrology and Hypertension, Friedrich-Alexander University, Erlangen-Nuremberg (FAU), Erlangen, Germany
3 Division of Neuroradiology, Friedrich-Alexander University, Erlangen-Nuremberg (FAU), Erlangen, Germany
4 International Neuroscience Institute, Hannover, Germany
5 Institute of Radiology and Nuclear Medicine, Paracelsus Private Medical University, Salzburg, Austria
6 Department of Neurosurgery, German Armed Forces Hospital Koblenz, Koblenz, Germany
7 Department of Radiology, Friedrich-Alexander University, Erlangen-Nuremberg (FAU), Germany

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© 2021 Manava et al.

open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: ( This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

* Address correspondence to this author at the Institute of Radiology and Nuclear Medicine, Paracelsus Private Medical University, Nuremberg Campus, Prof. Ernst-Nathan Str. 1, 90419 Nuernberg, Germany; Tel: +49 911-398-114930; E-mail:



In this study, we attempted to identify clinical parameters predicting the absence or presence of Neurovascular Compression (NVC) at the Ventrolateral Medulla (VLM) in arterial hypertension (HTN) in MRI findings.


Cardiovascular and pulmonary afferences are transmitted through the left vagus and glossopharyngeal nerve to the brain stem and vasoactive centers. Evidence supports the association between HTN and NVC at the left VLM. Several independent studies indicate a reduction of HTN after Microvascular Decompression (MVD) of the left. Several independent studies indicate a reduction of HTN after Microvascular Decompression (MVD) of the left VLM. Image processing of MRI provides comprehensible detection of NVC. HTN affects hemodynamic parameters and organs.


This study analyzes and correlates clinical data and MRI findings in patients with and without NVC at the VLM in treatment resistant HTN to obtain possible selection criteria for neurogenic hypertension.


In 44 patients with treatment resistant HTN, we compared MRI findings of neurovascular imaging to demographic, clinical and lifestyle data, office and 24-hour ambulatory Blood Pressure (BP), and cardiovascular imaging and parameters.


Twenty-nine (66%) patients had evidence of NVC at the VLM in MRI. Sixteen patients (36%) had unilateral NVC on the left side, 7 (16%) unilateral right and 6 (14%) bilateral NVC. Fifteen (34%) had no evidence of NVC at the VLM. Patients with left sided NVC were significantly younger, than those without NVC (p=0.034). They showed a statistically significant variance in daytime (p=0.020) and nighttime diastolic BP (p<0.001) as the mean arterial pressure (p=0.020). Other measured parameters did not show significant differences between the two groups.


We suggest to examine young adults with treatment resistant HTN for the presence of NVC at VLM, before signs of permanent organ damage appear. Clinical and hemodynamic parameters did not emerge as selection criteria to predict NVC. MVD as a surgical treatment of NVC in HTN is not routine yet as a surgical treatment of NVC in HTN is not routine yet. Detection of NVC by imaging and image processing remains the only criteria to suggest MVD, which should be indicated on an individual decision.

Keywords: Neurovascular compression, Hypertension, Ventrolateral medulla, Image fusion, Neuroimaging, MRI.


NVC describes a pathological contact between the Root Entry/Exit Zone (REZ) of a cranial nerve and a vessel at the brain stem, resulting in a hyperactive dysfunction. A possible etiologic association between NVC at the left VLM and arterial HTN was noticed by JANNETTA et al. [1]. A significant reduction of arterial HTN was observed after microvascular decompression (MVD) [1-3]. A microanatomical study classified the NVC at the VLM in HTN [4, 5]. Animal models have defined the role of the sympathoexcitatory neurons of the rostral VLM and the inhibitory neurons of the caudal VLM in blood pressure regulation [4]. It seems that NVC at the VLM leads to a permanent irritation and activation of the C1 neurons located at the VLM. A possible explanation for the left NVC in essential HTN is the additional compression of the REZ of the ninth and 10th Cranial Nerves (CN IX-X). The major part of the afferent inputs from the myocardial receptors of the left ventricle and atrium to the nucleus tractus solitarii are conducted by the low-myelinated cardiac c-fibers of the left vagus nerve [4]. Several imaging studies supported the evidence of NVC [6-10] opposed by other studies, which could not find a significant association [11-17]. JANNETTA’s surgical results were verified in multiple independent short and long term studies [2, 3, 6]. Elevated sympathetic nerve activity was observed in hypertensive patients with NVC at VLM in magnetic resonance imaging (MRI) [18, 19].

Physical parameters characterizing body size, such as Body Mass Index (BMI), are associated with an elevated BP. HTN itself results in target organ damage like myocardial hypertrophy and vascular changes, which also result in abnormal parameters detected by physical examination and cardiovascular imaging. Elevated BP is present in approximately 80% of patients with ischemic stroke [20, 21]. Furthermore, BP variability (BPV) is an independent cardiovascular risk factor in hypertensive patients [22].

It seems that NVC of the left VLM is correlated to HTN, but only a few studies on the cause and the treatment, either clinical [1, 2, 23, 24] or experimental [1, 25-28], have been reported in the literature despite the possibility that such a neurogenic mechanism might be implicated in a relatively large number of patients [29], so this hypothesis of neurogenic hypertension still remains an object of debate.

The concept of vascular compression of the VLM as a mediator of increased BP via sympathetic stimulation is intriguing and may prove relevant in various clinical scenarios associated with elevated BP and its consequences, including stroke [30]. Until now, there exists no study correlating 3D- visualizations of MRI for detection of NVC at the VLM to hemodynamic and clinical parameters of patients with HTN. In this study, we attempted to identify clinical parameters predicting the absence or presence of NVC in HTN.

The study protocol with the number: 2633 was approved by the local ethics committee and performed according to the Declaration of Helsinki and the guidelines for “Good Clinical Practice” (GCP). Before enrollment, each patient provided written informed consent prior to inclusion in this observational study. The main results with respect to the outcome, BP and sympathetic activity have been previously published [18].


2.1. Clinical Data

The study cohort consisted of 44 patients (8 women and 36 men, age range 32-70 years, mean 57.5 years) with treatment resistant HTN, defined as office BP ≥140/90 mmHg (mean of two measurements), while treated with at least 3 antihypertensive drugs, one of which was a diuretic [31]. True treatment resistant HTN was confirmed by 24-hour ambulatory BP measurements (average 24-hour BP ≥ 130/80 mmHg). All patients were consecutively enrolled and referred to our University outpatient service to rule out secondary causes of HTN and discuss with the patient alternative interventional therapies.

In this prospective observational study, the following clinical parameters were obtained: age, gender, height, weight, body surface (BSA), BMI, family history of HTN, known duration of HTN (months), and duration of medical therapy. Furthermore, with the aid of questionnaires the following parameters were assessed: alcohol consumption (g/week), sporting activity (hours/week) and consumption of nicotine (pack years).

The patients were on a typical Bavarian diet without any restrictions, including salt intake. Otherwise, we would have needed a metabolic ward, which requires a completely different setting.

2.2. Blood Pressure Measurements

Office systolic and diastolic BP as well as heart rate (HR) were captured according to European Society of Hypertension/European Society of Cardiology (ESH/ESC) guideline recommendations. Additionally, we measured the casual systolic and diastolic BP (in mmHg) and the HR (heartbeats/minute) 3 minutes after standing up. Ambulatory 24-hour BP measurements provided averages of 24-hour systolic and diastolic BP, daytime and night-time diastolic and systolic BP, 24 h ambulatory HR and 24 h ambulatory mean arterial pressure. Daytime measurements were taken every 15 minutes and nighttime measurements every 30 minutes. As quality criteria, at least 50 measurements have been successfully completed over a 24-hour period in order to be entered into the database.

2.3. Cardiovascular Parameters

In all patients, a two-dimensional (2-D) guided amplitude mode (A-Mode) echocardiography was conducted to assess left ventricular structure and function. Septal wall thickness, posterior wall thickness and left ventricular mass were calculated, as previously recommended [32].

For an accurate and precise noninvasive determination of left ventricular mass and volume, cardiac MRI was applied [33, 34]. The prognostic significance of left ventricular function was well established. All subjects were imaged on a Siemens Symphony and Sonata MRI (Siemens AG, Erlangen, Germany). Cine images were acquired in 6 equally spaced short-axis locations from apex to base and 3 long-axis locations orthogonal to the short axis and orientated at 60° increments around the left ventricular central axis [34].

A 12-lead electrocardiogram (ECG) was recorded at rest in supine position and the electrocardiographic criteria of left ventricular hypertrophy (LVH) were analyzed: Sokolow-Lyon-Voltage-Index [35] and Cornell voltage duration product (Cornell) [36], heart rate and QT-time (in seconds) were obtained. To measure central systolic pressure and central pulse pressure, radial arterial wave form was recorded by the Sphygmocor System (Atcor-CardieX, New South Wales, Australia) and corresponding central aortic wave form were then automatically generated through a validated transfer function. In addition, pulse wave velocity was measured as a marker of arterial stiffness.

2.4. Imaging Procedures and Image Processing of NVC

Imaging was performed on a 3 Tesla MR System (Magnetom Trio, Siemens AG, Erlangen, Germany). High-resolution Constructive Interference in Steady State (CISS) (repetition time (TR) 7.48 ms, Time of Echo (TE) 3.23 ms, flip angle 45°, acquisition time 8:23 min:sec, matrix 512 x 512, number of slices 144, voxel size 0.4) and a 3D-TOF Angiogram (TR 21 ms, TE 3.77 ms, flip angle 18°, acquisition time 15:51 min:sec, matrix 512 x 512, number of slices 144, voxel size 0.4) were acquired. Image processing was applied to depict neurovascular relationships according to a specific protocol [37-39].

With this technique, we produced 3D representations of the brain stem and cranial nerves together with the vessels at the surface of the brain stem in each individual [38]. The relationships between cranial nerves and vessels, especially at the VLM were analyzed regarding the existence of NVC by two independent expert observers. The location and type of NVC [4] were determined (Fig. 1). The presence or absence of NVC in the 3D representations divided the patients into two groups. The obtained clinical and hemodynamic parameters were correlated between the two groups.

Fig. (1). a-b Image Processing [37]; c-d: 3D-Visualization of the MR-Data of a patient with treatment resistant HTN. The arrows are pointing at the NVC on the REZ of N.IX. and N.X.

In addition, an axial T2-weighted turbo spin echo sequence (T2w TSE), coronar fluid attenuated inversion recovery (FLAIR), axial T1-weighted turbo spin echo sequence (T1w TSE) and diffusion weighted sequence (DWI) of the standard mri protocol were acquired and analyzed. The coronar FLAIR and transversal T2-weighted sequence were used to determine the degree of deep and periventricular white matter lesions (WMLs). The Fazekas score was used for the classification of WMLs [40].

2.5. Statistics

Clinical variables were compared between the two groups using a Mann-Whitney-U-Test. Over all groups, a Levene’s Test was applied to assess the equality of variances of the values. A standard level of statistical significance (p <0.05) was used and data were reported with 95% confidence intervals. The statistical analysis was performed using SPSS (IBM SPSS Statistics, Version 25).


3.1. Anatomical Results

All 44 patients underwent brain MRI and image processing was performed for all MRI images. Twenty-nine patients (66%) had evidence of NVC at the VLM. The left side was affected in 16 patients (36%) and the right side in 7 patients (16%). We observed a bilateral NVC in 6 (14%) patients. No NVC (either left or right) was seen in 15 (34%) patients (Table 1). The total number of NVC observed on the left is 22 and on the right side 13 (Table 1). According to a previously published classification [4], we found NVC type I in 16 patients, NVC type II in 4 patients and NVC type III on the left VLM in 2 patients. On the right VLM, 10 patients had an NVC type I, 2 patients a NVC type II and 1 patient a NVC type III.

Patients were separated into two groups characterized by cases with left NVC including bilateral NVC (“NVC left all”) and all cases without NVC on the left including cases showing NVC right (“No NVC left”); (Table 1). Overall, we had 22 cases as “NVC left all” and 22 cases as “no NVC left”.

Women were affected in 4 of the 22 cases of left NVC and men in 18 cases. Similar results were found in the group without NVC left with 4 women and 18 men; there was no difference between gender and the detection of left NVC (χ2 = 0.00, p = 1.0).

3.2. Comparison of Clinical Data

3.2.1. Comparison of Body Characteristics, Behavior and Lifestyle

We analyzed age, BMI, alcohol consumption, sporting activity, nicotine consumption in pack-years and the duration of hypertension. Two patients lacked information about their smoking behavior. The group variances in age were not homogeneous (p=0.018) (Table 2).

There was a significant difference in age between the two groups (median NVC left all= 57, no NVC left = 63; p=0.034; (Table 3a and Fig. 2). There were no significant differences among the two groups in gender, medical history, duration of HTN (NVC left all: 164.55 months, no NVC left: 202.68 months), smoking (NVC left all: 8.63 months, no NVC left: 15.71 months) and alcohol consumption (NVC left all: 152.27 g/week, no NVC left: 181.02 g/week) (Table 3a).

Fig. (2). Age distribution in years in the two groups “NVC left al”lvsno NVC left”. Box= 25th and 75th percentiles; bars =min and max values. Data not included is marked with a small circle. Levene’s Test (p=0.018), Mann-Whitney-U-test (p=0.034).

Table 1. Frequency distribution of the NVC groups.
Groups Prevalence Percent in %
Left NVC 16 36.40
Right NVC 7 15.90
Bilateral NVC 6 13.60
No NVC 15 34.10
NVC left all (left NVC + bilateral NVC) 22 50.00
No NVC left (no NVC + right NVC) 22 50.00
Table 2. Levene’s test for equality of error of variances.
- Levene’s -Test for equality of Variance
F Significance
AGE Equal variance assumed 6.116 0.018
Equal variance not assumed
Daily diastolic BP Equal variance assumed 4.370 0.043
Equal variance not assumed
Nighttime systolic BP Equal variance assumed 1.028 0.317
Equal variance not assumed
Nighttime diastolic BP Equal variance assumed 17.085 0.000
Equal variance not assumed
Nighttime Mean arterial pressure Equal variance assumed 7.236 0.010
Equal variance not assumed
Day- and nighttime systolic BP Equal variance assumed 2.324 0.135
Equal variance not assumed
Day- and nighttime diastolic BP Equal variance assumed 9.704 0.003
Equal variance not assumed
Day- and nighttime Mean arterial pressure Equal variance assumed 5.898 0.020
Pulse wave velocity Equal variance assumed 0.12 0.912
Equal variance not assumed
Table 3a-e. Clinical variables were compared between the two groups using a Mann-Whitney-U-Test.
Parameters NVC left N Mean Std.-deviation P Value
Patients specific body characteristics, behavior and lifestyle (3a): - - - - -
AGE (years) Yes 22 56.00 9.68 0.034
No 22 61.32 5.63
BMI (kg/m2) Yes 22 29.20 3.09 0.944
No 22 29.48 4.08
Alcohol consumption (g/week) Yes 22 152.27 138.85 0.509
No 22 181.02 151.41
Sporting activity (hours/week) Yes 22 2.22 2.7287 0.162
No 22 1.341 2.4562
Nicotine pack years Yes 20 8.63 13.39 0.309
No 22 15.71 20.37
Duration of hypertension (months) Yes 22 164.55 118.19 0.301
No 22 202.68 143.10
Comparison of BP and vascular parameters (3b): NVC left N Mean Std.-deviation P Value
Casual systolic BP (mmHg) Yes 22 158.10 19.65 0.614
No 22 161.68 19.41
Casual diastolic BP (mmHg) Yes 22 94.86 12.81 0.823
No 22 93.96 11.18
Casual Heart Rate (bpm) Yes 22 66.14 15.61 0.778
No 22 64.77 11.83
Casual syst. BP after 3 min Standing (mmHg) Yes 22 158.10 17.64 0.725
No 22 159.36 17.31
Casual diast. BP after 3 min. Standing (mmHg) Yes 22 95.18 11.74 0.953
No 22 95.36 9.76
Casual Heart Rate after 3 min. Standing (mmHg) Yes 21 65.71 13.19 0.313
No 22 69.32 14.58
Daytime systolic BP (mmHg) Yes 21 144.19 16.30 0.465
No 22 147.50 11.64
Daytime diastolic BP (mmHg) Yes 21 88.86 11.69 0.971
No 22 88.64 7.09
Daytime Mean arterial Pressure (mmHg) Yes 21 108.48 12.69 0.473
No 21 109.86 7.60
Daytime Heart Rate (bpm) Yes 21 68.62 10.95 0.381
No 22 69.27 11.94
Nighttime systolic BP (mmHg) Yes 21 128.71 18.73 0.155
No 22 135.64 14.23
Nighttime diastolic BP (mmHg) Yes 21 76.10 13.76 0.331
No 22 77.41 5.70
Nighttime Mean Arterial Pressure (mmHg) Yes 21 94.71 14.81 0.199
No 21 97.91 8.01
Nighttime Heart Rate (bpm) Yes 21 61.33 8.73 0.913
No 22 61.36 9.81
Day- and Nighttime syst. BP (mmHg) Yes 21 139.29 15.96 0.243
No 22 144.14 10.80
Day- and nighttime diast. BP (mmHg) Yes 21 84.95 11.90 0.697
No 22 85.32 5.96
Day- and nighttime Mean arterial Pressure (mmHg) Yes 21 104.14 12.76 0.284
No 21 106.33 6.61
Day- and nighttime Heart Rate (bpm) Yes 21 66.43 9.94 0.488
No 22 66.96 10.96
Comparison of ECG data (3c) NVC left N Mean Std.-Deviation P Value
Heart Rate (bpm) Yes 22 59.50 10.43 0.934
No 22 59.23 10.43
QT Yes 22 427.32 31.61 0.613
No 22 422.46 23.06
Sokolov-Lyon-Index Yes 22 2.59 0.8485 0.259
No 22 2.26 0.8156
Cornell-Index Yes 21 1.96 0.7807 0.125
No 22 1.59 0.5525
Comparison of Echocardiographic Data (3d) NVC left N Mean Std.-Deviation P Value
Posterior Wall Thickness Diastolic (mm) Yes 21 11.62 1.21 0.11
No 21 10.79 1.67
Posterior Wall Thickness Systolic (mm) Yes 21 18.04 1.95 0.545
No 21 17.68 2.40
Septum Thickness Diastolic (mm) Yes 21 12.76 1.55 0.344
No 21 12.16 2.21
Septum Thickness Systolic (mm) Yes 21 18.04 2.26 0.457
No 21 17.44 3.24
Comparison of Cardiac MRI data (3d) NVC left N Mean Std.-Deviation P Value
Left ventricular wall (in grams) Yes 22 148.50 25.20 0.606
No 20 149.25 37.69
Right ventricular wall (in grams) Yes 19 40.79 8.83 0.754
No 20 40.48 8.73
Pulse Wave Analysis (3e) NVC left N Mean Std.-Deviation P Value
Peripheral systolic Pressure (mmHg) Yes 22 156,41 23,38 0,581
No 22 159,27 21,51
Peripheral Diastolic pressure (mmHg) Yes 22 91,50 12,83 0,597
No 22 93,23 11,51
Peripheral Mean Pressure (mmHg) Yes 22 115,36 15,93 0,69
No 22 117,00 14,77
Peripheral Augmentation Index (%) Yes 22 33,50 10,75 0,778
No 22 35,64 8,03
Aortic Systolic Pressure (mmHg) Yes 22 148,36 23,70 0,511
No 22 151,82 21,19
Aortic diastolic Pressure (mmHg) Yes 22 92,55 12,97 0,69
No 22 94,14 11,95
Aortic augmentation pressure (mmHg9 Yes 22 20,09 10,45 0,581
No 22 20,77 7,73
Aortic augmentation index (%) Yes 22 25,46 10,06 0,596
No 22 27,55 7,65
Pulse wave velocity Yes 17 9,97 1,71 0,987
No 18 10,18 1,91

3.2.2. Comparison of BP, ECG and Vascular Parameters

The systolic casual BP in patients with left NVC was measured with a mean value of 158.10 (SD 19.65) mmHg in comparison to the cases without NVC left with 161.68 (SD 158.10) mmHg. In the variances of the measurements of 24-h-BP, statistical significances could be found especially in the night measurements between the two group; nighttime diastolic BP (NVC left all: 76.10 mmHg, SD 13.76; no NVC left all: 77.41mmHg, SD 5.7; p<0.001), nighttime mean arterial pressure (MAP) (NVC left all: 94.71 mmHg, SD 14.81; no NVC left all: 97.91 mmHg, SD 8.01; p=0.010), day- and nighttime diastolic BP (NVC left all: 84.95 mmHg, SD 11.90; no NVC left: 85.32 mmHg, SD 5.96; p=0.003) and day- and nighttime MAP (NVC left all: 104.14 mmHg, SD 12.76; no NVC left: 106.33 mmHg, SD 6.61; p=0.020), (Figs. 3 and 4).

24-h-BP measurements and office systolic and diastolic BP showed no statistical differences between the two groups (Tables 3b and 3c). One patient did not participate in the 24-h-BP measurements.

3.2.3. Comparison of Echocardiographic and Cardiac MRI Data

No differences were found between the two groups in any of the cardiac MRI and echocardiographic data with a posterior wall thickness of 11.62 mm diastolic in the group of left NVC all and 10.79 mm in the group without NVC left (Table 3d). The systolic posterior wall thickness was 18.04 mm in NVC left all and 17.68 mm in no NVC left similar. We obtained cardiac MRI data in 42 patients. The right ventricular wall could be measured only in 39 patients due to artifacts.

3.2.4. Comparison of Pulse Wave Analysis (PWA) and Pulse Wave Velocity (PWV)

There were no significant differences among the two groups in the measurements of PWA and PWV (Table 3e). Pulse wave velocity was measured in 35 patients.

3.2.5. Data on Antihypertensive Medication

Table 4 presents the medication profile between the two groups, where no differences could be found. In the group “NVC left all”, 12 patients received an ACEI’s and 12 patients and ARB’s. A combination of both were given only in 2 cases with left NVC all. In the group without left NVC, 11 patients received ACEI’s, 14 patients ARB’s and a combination in 3 cases.

All patients received thiazide type diuretics. 18 cases of left NVC all received CCB and only 8 cases received CCB in the group no NVC left. Beta-blockers were given to 15 patients with left NVC and 9 patients without NVC. Central sympatholytic drugs were given to six patients with NVC left and to four patients without NVC.

Fig. (3). Nighttime systolic (N_SBP) and diastolic BP (N_DBP) and the mean arterial pressure (N_MAP) obtained from 24-h-measurements of BP. Box= 25th and 75th percentiles; bars =min and max values. Levene’s Test (N_SBP p=0.317; N_DBP p< 0.001; N_MAP p= 0.01) Mann-Whitney-U-test (N_SBP p=0,155; N_DBP p=0.331; N_MAP p=0.199).

Fig. (4). 24-hour ambulatory (DN_SBP) systolic and (DN_DBP) diastolic BP as well as mean arterial pressure (DN_MAP) obtained from 24-h-measurements of BP. Box= 25th and 75th percentiles; bars =min and max values. Data not included is marked with a small circle. Levene’s Test (DN_SBP p=0.135; DN_DBP p=0.003; DN_MAP p=0.020). Mann-Whitney-U-test (DN_SBP p= 0.234; DN_DBP p=0.687; DN_MAP p=0.284).

Table 4. Pharmacologic management of the Patients with and without NVC left.
Pharmacologic Management NVC Left All No NVC Left
ACEI‘s 12 11
ARB‘s 12 14
Combination of ACEI’s and ARB’s 2 3
Thiazide type diuretics 22 22
CCB 18 8
Beta-blockers 15 9
Central symphatholytic drugs 6 4
Alpha-blockers 2 5

3.2.6. Analysis of WMLs

WMLs could be found in 11 cases in NVC left, 9 of those with moderate findings (Score 1) and 2 patients with severe findings (Score 2). In the group without NVC, we found WMLs in 14 cases, of those 10 with moderate findings (Score 1) and 4 with severe changes (Score 2) according to Fazekas.


In this study, we tried to identify specific patterns of clinical and hemodynamic data of hypertensive patients which may indicate the presence of an NVC at the VLM. MVD can be an option for therapy in patients with severe HTN refractory to medical therapy [41]. The long term results after MVD in patients with essential HTN and NVC show that surgery could be a successful alternative therapy in certain subgroups of patients with HTN [3].

Several studies have already demonstrated an association between NVC and elevated sympathetic activity [10, 19, 42, 43]. An elevated sympathetic activity is associated with an elevation of left ventricular mass [33, 44]. Our data showed no significant difference between hypertensive patients with or without NVC in the chamber sizes and functions obtained by CMR and echocardiography. This could be explained by the nearly equal duration of HTN in both groups (p=0.301). LVH appears in all types of HTN independent of the respective cause.

Correlation between vessel contact with the left retroolivary sulcus and higher plasma norepinephrine concentrations with depressor response to clonidine support the theory that vascular contact on the VLM may contribute to neurogenic mediated essential HTN [19].

Our group cohorts were similar in regard to gender differences. The same number of women and men were affected in both groups, with a higher frequency of men.

The structural changes regarding the WMLs in brain MRI were also similar in the two groups.

The significantly lower mean age (median: NVC left all= 57; no NVC left all=63; p=0.034) and greater variance (p=0.018) in the group NVC left all indicate that NVC can appear in younger patients and may develop faster into a treatment resistant HTN. Patients in the group “no NVC left”, demonstrate a more homogenous age distribution, (Fig. 2).

From the 24-h-BP measurements, we could identify a statistically significant difference of variance for daytime (p=0.020) and nighttime diastolic BP (p<0.001) as well as mean arterial pressure (p=0.020) between both groups and not interindividual as previously reported [21], (Figs. (3 and 4). This might be explained by a still existing autonomic regulation of BP in cases with NVC.

We could not find any significant differences between the two groups for PWA and PWV. This might be explained by the nearly similar duration of HTN in both groups. Organ damage is the same in all types of HTN, independent of the cause of HTN.

Since JANNETTA’s first suggestion of an association between arterial HTN and NVC of the left VLM and the REZ of the ninth and tenth cranial nerve (N.IX and N.X), a series of imaging studies with controversial results were published [6, 7, 10-16, 41, 43, 45, 46]. The meta-analysis of BOOGAARTS et al. [47] showed, a statistical significant higher prevalence of NVC at the left VLM in essential HTN as compared to normal control subjects. At this point, one may question whether all these studies are comparable, because some of them are retrospective [13, 16] and some of them are non-blinded studies [7, 16]. Several further aspects have to be taken into consideration in the meta-analysis. The first aspect is the precise definition and localization of NVC at the VLM and which structures are involved. Some studies did not give a precise description of how they define NVC and the respective region [11, 16]. A detailed anatomical examination of the NVC at the left VLM was published in an anatomic cadaveric study and described three distinct types of NVC associated with HTN [4]. Another aspect is the different quality of imaging. Some studies used high-resolution MRI and others used standard T1- or T2-weighted images with 3-5 mm slice thickness [7, 11, 13, 16, 45]. Nowadays, high resolution MR-sequences like CISS in combination with high resolution MR-Angiography (TOF) are widely accepted and considered as the appropriate sequences for evaluating the relationship between cranial nerves and vessels in the posterior cranial fossa [48-50]. One major aspect is the difference between prospective and retrospective studies and the quality of patient data collection regarding HTN. In our study, all patients received multiple workups over several years.

With the method used in this study, we introduced an advanced technique and standard for the evaluation of neurovascular relationships especially for the detection of NVC in essential HTN. With the use of this technique, it is possible to obtain 3D-presentations of NVC in HTN, which are reproducible.

Using 2D slice images as an exclusive source of information, an extensive experience on the part of the observer is required to achieve a correct assessment of the relationship of vessels and cranial nerves in the posterior cranial fossa. Hyperactive cranial nerve dysfunction syndromes require a comprehensive 3D analysis [38]. In this study, we used for the first time an advanced technique of image processing to generate 3D visualizations of the posterior cranial fossa in patients with HTN [39]. This was achieved through explicit segmentation of the cerebrospinal fluid (CSF), the brain stem and the cranial nerves, followed by implicit segmentation and separation of the vessels and cranial nerves embedded in CSF. Lastly, 3D visualizations were generated. The highest quality of the 3D visualization was achieved mostly through fusion of the CISS- and TOF- data. With this technique, nearly all the technical artifacts that may appear in this region, like the hemodynamic pulsation in the CSF were eliminated. Using these steps of image processing as previous introduced [48] and described [38, 39], we were able to have an exact and comprehensible anatomical representation of each patient (Fig. 1).

The literature affords robust anatomical and physiological evidence that compression of REZ of CN IX-X and adjacent VLM – especially on the left side, is known to convey inputs from the baroreceptors of the (left-sided) cardiac atrium – could be the origin of systemic arterial HTN [29]. JANNETTAS’ results were confirmed in several surgical studies [1-3, 29, 51] with short and long term results.

NVC of the VLM has also been detected in brachydactyly associated with HTN [52]. The latest genetic studies on HTN and its association with brachydactyly strongly suggest that mutations in PDE3A are responsible for HTN by contributing to a general increase in peripheral vascular resistance in this syndrome [53]. Until now, we have no data regarding PDE3A from our patients.

Previous reports showed that compression of VLM was closely associated with BP variability in the subacute ischemic stroke phase [21]. Elevated BP is present in approximately 80% of patients with ischemic strokes [54]. As with intracranial aneurysms, a wide range of BP variability seems to be also relevant for NVC in HTN [55, 56]. Further studies are necessary to find possible correlations.

The small number of patients could be considered as a limitation of our study. However, this could be explained by highly selective criteria for diagnosis of treatment resistant HTN as well as the availability of all clinical and hemodynamic parameters. Further large and detailed clinical studies will be needed to elucidate the clinical factors to influence the interaction between increased BP variance and the detection of NVC at the left VLM.


NVC of the VLM can be detected in patients with arterial HTN. Young patients with arterial, treatment resistant HTN should be examined for the presence of NVC at the VLM before permanent organ damage occurs. The possible association of NVC in HTN and the detailed analysis of 24 h BP regarding the BP variability should be further evaluated. Clinical and hemodynamic parameters do not sufficiently indicate the presence of NVC. Possible candidates for MVD can only be identified after confirming a positive finding of NVC with the use of MRI.


All authors contributed to the study's conception and design. Material preparation, data collection and analysis were performed by Panagiota MANAVA, Ramin NARAGHI and Peter HASTREITER. The first draft of the manuscript was written by Panagiota MANAVA and all authors commented on the previous versions of the manuscript. All authors read and approved the final manuscript.


This study was approved by the ethics committee of the University Erlangen-Nuremberg (FAU) in Erlangen, Germany with the ethical approval number: 2633.


No animals were used in this research. All human research procedures followed were in accordance with the ethical standards of the committee responsible for human experimentation (institutional and national), Declaration of Helsinki and the guidelines for “good clinical practice” (GCP).


Each patient provided written informed consent prior to inclusion in this observational study.


The data supporting the findings of the article is available from corresponding author [P.M] upon reasonable request.


This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.


We wish to confirm that there are no known conflicts of interest associated with this publication and there has been no financial support for this work that could have influenced its outcome.


This article is dedicated to Peter J. Jannetta (*April 05. 1932 - †April 11. 2016) for his pioneer work on neurovascular compression at the ventrolateral medulla and arterial hypertension.


[1] Jannetta PJ, Segal R, Wolfson SKJ Jr. Neurogenic hypertension: etiology and surgical treatment. I. Observations in 53 patients. Ann Surg 1985; 201(3): 391-8.
[2] Geiger H, Naraghi R, Schobel HP, Frank H, Sterzel RB, Fahlbusch R. Decrease of blood pressure by ventrolateral medullary decompression in essential hypertension. Lancet 1998; 352(9126): 446-9.
[3] Frank H, Schobel HP, Heusser K, Geiger H, Fahlbusch R, Naraghi R. Long-term results after microvascular decompression in essential hypertension. Stroke 2001; 32(12): 2950-5.
[4] Naraghi R, Gaab MR, Walter GF, Kleineberg B. Arterial hypertension and neurovascular compression at the ventrolateral medulla. A comparative microanatomical and pathological study. J Neurosurg 1992; 77(1): 103-12.
[5] Kleineberg B, Becker H, Gaab MR. Neurovascular compression and essential hypertension. An angiographic study. Neuroradiology 1991; 33(1): 2-8.
[6] Naraghi R, Geiger H, Crnac J, Huk W, Fahlbusch R, Engels G, et al. Posterior fossa neurovascular anomalies in essential hypertension. The Lancet 1994; 344: 1466-70.
[7] Akimura T, Furutani Y, Jimi Y, et al. Essential hypertension and neurovascular compression at the ventrolateral medulla oblongata: MR evaluation. AJNR Am J Neuroradiol 1995; 16(2): 401-5.
[8] Makino Y, Kawano Y, Okuda N, et al. Autonomic function in hypertensive patients with neurovascular compression of the ventrolateral medulla oblongata. J Hypertens 1999; 17(9): 1257-63.
[9] Morimoto S, Sasaki S, Miki S, et al. Pulsatile compression of the rostral ventrolateral medulla in hypertension. Hypertension 1997; 29(1 Pt 2): 514-8.
[10] Sendeski MM, Consolim-Colombo FM, Leite CC, Rubira MC, Lessa P, Krieger EM. Increased sympathetic nerve activity correlates with neurovascular compression at the rostral ventrolateral medulla. Hypertension 2006; 47(5): 988-95.
[11] Colón GP, Quint DJ, Dickinson LD, et al. Magnetic resonance evaluation of ventrolateral medullary compression in essential hypertension. J Neurosurg 1998; 88(2): 226-31.
[12] Hohenbleicher H, Schmitz SA, Koennecke HC, et al. Neurovascular contact of cranial nerve IX and X root-entry zone in hypertensive patients. Hypertension 2001; 37(1): 176-81.
[13] Johnson D, Coley SC, Brown J, Moseley IF. The role of MRI in screening for neurogenic hypertension. Neuroradiology 2000; 42(2): 99-103.
[14] Säglitz SA, Gaab MR. Investigations using magnetic resonance imaging: is neurovascular compression present in patients with essential hypertension? J Neurosurg 2002; 96(6): 1006-12.
[15] Thuerl C, Rump LC, Otto M, et al. Neurovascular contact of the brain stem in hypertensive and normotensive subjects: MR findings and clinical significance. AJNR Am J Neuroradiol 2001; 22(3): 476-80.
[16] Watters MR, Burton BS, Turner GE, Cannard KR. MR screening for brain stem compression in hypertension. AJNR Am J Neuroradiol 1996; 17(2): 217-21.
[17] Zizka J, Ceral J, Elias P, et al. Vascular compression of rostral medulla oblongata: prospective MR imaging study in hypertensive and normotensive subjects. Radiology 2004; 230(1): 65-9.
[18] Schobel HP, Frank H, Naraghi R, Geiger H, Titz E, Heusser K. Hypertension in patients with neurovascular compression is associated with increased central sympathetic outflow. J Am Soc Nephrol 2002; 13(1): 35-41.
[19] Gajjar D, Egan B, Curè J, Rust P, VanTassel P, Patel SJ. Vascular compression of the rostral ventrolateral medulla in sympathetic mediated essential hypertension. Hypertension 2000; 36(1): 78-82.
[20] Chung JW, Kim N, Kang J, et al. Blood pressure variability and the development of early neurological deterioration following acute ischemic stroke. J Hypertens 2015; 33(10): 2099-106.
[21] Nezu T, Hosomi N, Kuzume D, et al. Effects of vascular compression on the rostral ventrolateral medulla for blood pressure variability in stroke patients. J Hypertens 2020; 38(12): 2443-50.
[22] Del Giorno R, Balestra L, Heiniger PS, Gabutti L. Blood pressure variability with different measurement methods: Reliability and predictors. A proof of concept cross sectional study in elderly hypertensive hospitalized patients. Medicine (Baltimore) 2019; 98(28): e16347-.
[23] Levy EICB, Clyde B, McLaughlin MR, Jannetta PJ. Microvascular decompression of the left lateral medulla oblongata for severe refractory neurogenic hypertension. Neurosurgery 1998; 43(1): 1-6.
[24] Naraghi R, Fahlbusch R, Eds. Microvascular decompression for the treatment of hypertension 2001.
[25] Jannetta PJ Sr, Segal R, Wolfson SK Jr, Dujovny M, Semba A, Cook EE. Neurogenic hypertension: etiology and surgical treatment. II. Observations in an experimental nonhuman primate model. Ann Surg 1985; 202(2): 253-61.
[26] Segal R, Gendell HM, Canfield D, Dujovny M, Jannetta PJ. Cardiovascular response to pulsatile pressure applied to ventrolateral medulla. Surg Forum 1979; 30: 433-5.
[27] Segal R, Gendell HM, Canfield D, Dujovny M, Jannetta PJ. Hemodynamic changes induced by pulsatile compression of the ventrolateral medulla. Angiology 1982; 33(3): 161-72.
[28] Segal R, Jannetta PJ, Wolfson SK, Dujovny M, Cook EE. Implanted pulsatile balloon divice for simulation of neurovascularcompression. J Neurosurg 1982; 57: 646-50.
[29] Sindou M, Mahmoudi M, Brînzeu A. Hypertension of neurogenic origin: effect of microvascular decompression of the CN IX-X root entry/exit zone and ventrolateral medulla on blood pressure in a prospective series of 48 patients with hemifacial spasm associated with essential hypertension. J Neurosurg 2015; 123(6): 1405-13.
[30] Schlaich MP, Nolde JM, Carnagarin R, Schlaich LI, Kiuchi MG. Vascular compression of the rostral ventrolateral medulla: a relevant indicator of sympathetically driven blood pressure variability? J Hypertens 2020; 38(12): 2380-1.
[31] Mancia G, Fagard R, Narkiewicz K, et al. 2013 ESH/ESC Guidelines for the management of arterial hypertension: the Task Force for the management of arterial hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC). J Hypertens 2013; 31(7): 1281-357.
[32] Marwick TH, Gillebert TC, Aurigemma G, et al. Recommendations on the use of echocardiography in adult hypertension: A report from the european association of cardiovascular imaging (EACVI) and the american society of echocardiography (ASE). J Am Soc Echocardiogr 2015; 28(7): 727-54.
[33] Burns J, Sivananthan MU, Ball SG, Mackintosh AF, Mary DA, Greenwood JP. Relationship between central sympathetic drive and magnetic resonance imaging-determined left ventricular mass in essential hypertension. Circulation 2007; 115(15): 1999-2005.
[34] Cowan BR, Young AA, Anderson C, et al. Left ventricular mass and volume with telmisartan, ramipril, or combination in patients with previous atherosclerotic events or with diabetes mellitus (from the ONgoing Telmisartan Alone and in Combination With Ramipril Global Endpoint Trial [ONTARGET]). Am J Cardiol 2009; 104(11): 1484-9.
[35] Rautaharju PM, Surawicz B, Gettes LS, et al. AHA/ACCF/HRS recommendations for the standardization and interpretation of the electrocardiogram: part IV: the ST segment, T and U waves, and the QT interval: a scientific statement from the American Heart Association Electrocardiography and Arrhythmias Committee, Council on Clinical Cardiology; the American College of Cardiology Foundation; and the Heart Rhythm Society. J Am Coll Cardiol 2009; 53(11): 982-91.
[36] Casale PN, Devereux RB, Alonso DR, Campo E, Kligfield P. Improved sex-specific criteria of left ventricular hypertrophy for clinical and computer interpretation of electrocardiograms: validation with autopsy findings. Circulation 1987; 75(3): 565-72.
[37] Hastreiter P, Naraghi R, Tomandl B, Bonk A, Fahlbusch R. Analysis and 3-dimensional visualization of neurovascular compression syndromes. Acad Radiol 2003; 10(12): 1369-79.
[38] Naraghi R, Hastreiter P, Tomandl B, Bonk A, Huk W, Fahlbusch R. Three-dimensional visualization of neurovascular relationships in the posterior fossa: technique and clinical application. J Neurosurg 2004; 100(6): 1025-35.
[39] Manava P, Naraghi R, Schmieder R, Fahlbusch R, Doerfler A, Lell MM, et al. 3d-visualization of neurovascular compression at the ventrolateral medulla in patients with arterial hypertension. Clin Neuroradiol 2020.
[40] Fazekas F, Chawluk JB, Alavi A, Hurtig HI, Zimmerman RA. MR signal abnormalities at 1.5 T in Alzheimer’s dementia and normal aging. AJR Am J Roentgenol 1987; 149(2): 351-6.
[41] Ceral J, Zizka J, Eliás P, Solar M, Klzo L, Reissigová J. Neurovascular compression in essential hypertension: cause, consequence or unrelated finding? J Hum Hypertens 2007; 21(2): 179-81.
[42] Sasaki S, Tanda S, Hatta T, et al. Neurovascular decompression of the rostral ventrolateral medulla decreases blood pressure and sympathetic nerve activity in patients with refractory hypertension. J Clin Hypertens (Greenwich) 2011; 13(11): 818-20.
[43] Smith PA, Meaney JF, Graham LN, et al. Relationship of neurovascular compression to central sympathetic discharge and essential hypertension. J Am Coll Cardiol 2004; 43(8): 1453-8.
[44] Greenwood JP, Scott EM, Stoker JB, Mary DA. Hypertensive left ventricular hypertrophy: relation to peripheral sympathetic drive. J Am Coll Cardiol 2001; 38(6): 1711-7.
[45] Morimoto S, Sasaki S, Miki S, et al. Neurovascular compression of the rostral ventrolateral medulla related to essential hypertension. Hypertension 1997; 30(1 Pt 1): 77-82.
[46] Morise T, Horita M, Kitagawa I, et al. The potent role of increased sympathetic tone in pathogenesis of essential hypertension with neurovascular compression. J Hum Hypertens 2000; 14(12): 807-11.
[47] Boogaarts HD, Menovsky T, de Vries J, Verbeek AL, Lenders JW, Grotenhuis JA. Primary hypertension and neurovascular compression: a meta-analysis of magnetic resonance imaging studies. J Neurosurg 2012; 116(1): 147-56.
[48] Hastreiter P, Naraghi R, Tomandl BF, Bauer M, Fahlbusch R, Eds. 3D- visualization and registration for neurovascular compression syndrome analysis. MICCAI 02 Proc of 5th Int Conf on Med Img Comput and Comp-Assis Interv 2002.
[49] Leal PR, Hermier M, Froment JC, Souza MA, Cristino-Filho G, Sindou M. Preoperative demonstration of the neurovascular compression characteristics with special emphasis on the degree of compression, using high-resolution magnetic resonance imaging: a prospective study, with comparison to surgical findings, in 100 consecutive patients who underwent microvascular decompression for trigeminal neuralgia. Acta Neurochir (Wien) 2010; 152(5): 817-25.
[50] Tanrikulu L, Hastreiter P, Richter G, Doerfler A, Naraghi R. Virtual neuroendoscopy: MRI-based three-dimensional visualization of the cranial nerves in the posterior cranial fossa. Br J Neurosurg 2008; 22(2): 207-12.
[51] Niu X, Sun H, Yuan F, et al. Microvascular decompression in patients with hemifacial spasm. Brain Behav 2019; 9(11)e01432
[52] Naraghi R, Schuster H, Toka HR, et al. Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly. Stroke 1997; 28(9): 1749-54.
[53] Maass PG, Aydin A, Luft FC, et al. PDE3A mutations cause autosomal dominant hypertension with brachydactyly. Nat Genet 2015; 47(6): 647-53.
[54] Tikhonoff V, Zhang H, Richart T, Staessen JA. Blood pressure as a prognostic factor after acute stroke. Lancet Neurol 2009; 8(10): 938-48.
[55] Lanza G, Vinciguerra L, Puglisi V, et al. Acute isolated trochlear nerve palsy in a patient with cavernous carotid aneurysm and visit-to-visit variability in systolic blood pressure. Int J Stroke 2015; 10(6)E61
[56] Vagli C, Fisicaro F, Vinciguerra L, et al. Cerebral hemodynamic changes to transcranial doppler in asymptomatic patients with fabry’s disease. Brain Sci 2020; 10(8)E546