Literature DB >> 34232460

Aortic root dimensions as a correlate for aortic regurgitation's severity.

Jan-Per Wenzel1,2, Elina Petersen3, Julius Nikorowitsch4, Jessica Müller3, Tilo Kölbel5, Hermann Reichenspurner6,7, Stefan Blankenberg4,6,3, Evaldas Girdauskas6,7.   

Abstract

To evaluate the prevalence of aortic regurgitation (AR) and associations between the individual aortic root components and AR severity in the general population. The study included the first 10,000 participants of the population-based Hamburg City Health Study (HCHS) of whom 8259 subjects, aged 62.23 ± 8.46 years (51.3% females), enrolled 2016-2018, provided echocardiographic data. 69 subjects with bicuspid valves and 23 subjects with moderate/severe aortic stenosis were excluded. Aortic root dimensions were measured using state-of-the-art cardiac ultrasound, including the aortic annulus, sinus of Valsalva, sinotubular junction (STJ), and ascending aorta, in diastole and systole. The distribution of AR was: 932 (11.4%) mild, 208 (2.5%) moderate, and 20 (0.24%) severe. Patients with moderate or severe AR were predominantly male at advanced age who had hypertension, coronary artery disease, atrial fibrillation, and renal dysfunction. Increasing AR severity correlated with higher absolute and indexed aortic root diameters (e.g., end-diastolic sinus of Valsalva for no-mild-moderate-severe AR in mm ± standard deviation: 34.06 ± 3.81; 35.65 ± 4.13; 36.13 ± 4.74; 39.67 ± 4.61; p < 0.001). In binary logistic regression analysis, all aortic root components showed significant associations with moderate/severe AR. Mid-systolic STJ showed the strongest association with moderate/severe AR (OR 1.33, 95% confidence interval 1.25-1.43, p < 0.001). AR was prevalent in 14.2%, of whom 2.8% showed moderate/severe AR. All assessed aortic root diameters correlated with the prevalence and severity of AR. STJ diameter had the strongest association with moderate/severe AR possibly reflecting the pathophysiological impact of an increasingly dilated STJ in the context of an ageing aorta.
© 2021. The Author(s).

Entities:  

Keywords:  Aortic annulus; Aortic regurgitation; Aortic root; Echocardiography; Hamburg City Health Study; Sinotubular junction

Mesh:

Year:  2021        PMID: 34232460      PMCID: PMC8604845          DOI: 10.1007/s10554-021-02337-6

Source DB:  PubMed          Journal:  Int J Cardiovasc Imaging        ISSN: 1569-5794            Impact factor:   2.357


Introduction

The aortic root is a complex and dynamic entity, varying in size proportionally to height, weight, and age. The interplay of its four different parts, the aortic annulus (AoAn), sinus of Valsalva (SoV), sinotubular junction (STJ), and the proximal ascending aorta (AscAo), is crucial for aortic valve (AV) competence. Along with a dramatic decrease of rheumatic heart disease in the Western world, aortic root dilatation evolved into the predominant cause of aortic regurgitation (AR) [1-4]. However, AR is a multifactorial valvular disease and the correlation between the extent of aortic root dilatation and the severity of AR remains controversial [2, 3]. Notably, most previously published studies correlating AR with aortic root enlargement focused on the aortic root as one entity. Accordingly, little is known about the role of the individual components of the aortic root and their timepoint of measurement during the heart cycle in relation to AR, which is crucial to understand in the field of AV repair surgery. Furthermore, given major improvements in spatial and temporal resolution of 2-dimensional and color Doppler transthoracic echocardiography (TTE), most previous studies investigating AR prevalence and its correlation with aortic root diameter are rather outdated [2, 5–7]. Hence, first we aimed at providing up-to-date data on the prevalence of AR as assessed by state-of-the-art TTE in the general population. Second, we investigated the correlation between AR severity and each individual part of the aortic root measured systematically in end-diastole and mid-systole.

Methods

Study setting

The study population derived from a sample of 10,000 consecutive, at random selected participants from the Hamburg City Health Study (HCHS, www.hchs.hamburg) who underwent TTE. As previously described, the HCHS is a single-center, prospective, long-term, population-based cohort study [8]. HCHS aims to evaluate the interaction of socioeconomic risk factors, modern imaging techniques, physiological measurements, and clinical variables. All measurements were conducted between 2016 and 2018 during a one-day baseline visit at the HCHS Epidemiological Study Center Hamburg-Eppendorf, Germany according to the published study protocol [8]. Demographics and clinical parameters were assessed by standardized interviews conducted by specifically trained medical professionals following standard operating procedures as well as self-reported questionnaires [8]. Blood samples were withdrawn under fasting conditions and all subjects underwent biomarker quantification including NT-proBNP. After application of the exclusion criteria (1) incompletely recorded images or insufficient image quality of TTE for standardized measurements (1741) (2) moderate/severe aortic stenosis (23) or (3) bicuspid valve disease (69), 8167 subjects were included in the study. The study protocol was approved by the local ethics committee (PV5131, Medical Association Hamburg) and the HCHS steering board. All participants gave written informed consent. The investigation conforms with the principles outlined in the Declaration of Helsinki.

TTE image acquisition and analysis

TTE examinations were performed and analyzed by professional cardiologists and sonographers (technicians) at the baseline visit on dedicated ultrasound machines (Siemens Acuson SC2000 Prime, Siemens Healthineers, Erlangen, Germany) following standard operating procedures at the HCHS Epidemiological Study Center Hamburg-Eppendorf, Hamburg, Germany [8]. All TTE standard views were assessed in 2-dimensional echocardiography, including a 3-dimensional four-chamber view for chamber quantification. For continuous quality assessment, every 100th TTE exam was analyzed twice by an ESC TTE certified cardiologist. Qualitative and quantitative image analyses were performed using an off-line workstation with the commercially available and established Siemens syngo SC2000 software (Siemens syngo SC 2000 Version 4.0, Siemens Healthineers, Erlangen, Germany) in agreement with the current recommendations of the American Society of Echocardiography (ASE) and the European Association of Cardiovascular Imaging (EACVI) [9, 10]. Left sided volumes and ejection fraction (LVEF) were calculated using from two-dimensional and three-dimensional loops using the method of disks summation. Left-sided diameters were measured in parasternal long-axis view. Mitral inflow pattern was assessed in apical four-chamber view by placing pulsed-wave (PW) Doppler sample volume between mitral leaflet tips. PW tissue Doppler imaging (TDI) e’ velocity was measured in apical four-chamber view by placing the sample volume at the lateral and septal basal regions. Tricuspid annular plane systolic excursion (TAPSE) was obtained by M-mode echocardiography in the apical four-chamber view. Right ventricular fractional area change was assessed in a right ventricular focused four-chamber view. Left atrial global peak systolic strain was measured in apical four-chamber view by velocity vector imaging averaging global peak strain of all segments of the left atrium.

Aortic root and valve assessment

For aortic root assessment, a zoomed transthoracic parasternal long axis view was recorded at breath hold [10]. Systematic measurements of the aortic root were performed perpendicular to the proximal aorta axis in end-diastole (ED) as well as in mid-systole (MS) including the following: The (a) AoAn, (b) SoV, (c) STJ, and (d) AscAo (at 2 cm range from the STJ) were measured perpendicular to the proximal aorta axis. AoAn, STJ and AscAo were measured using the inner-edge to inner-edge convention while the SoV was measured using the leading-edge to leading-edge convention. AV morphology (i.e., bicuspid vs. tricuspid) and potential degenerative changes were assessed in the parasternal long axis, AV short axis and apical views. Aortic stenosis and regurgitation were assessed according to current ESC guidelines [11]. An in-depth description of valve assessment is provided in the supplements.

Statistical analysis

Continuous variables are given as mean ± standard deviation (SD). Categorical variables are given as absolute numbers and percentage of participants. Multiple group comparisons of different severities of AR were assessed by analysis of variance (ANOVA) for continuous variables and chi-squared test (χ2) for categorical variables. BSA was calculated using the DuBois formula. Aortic root measurements were divided by BSA to obtain indexed measurements. Correlation of these indexed measurements with AR severity as well as the ratio of sinotubular junction and aortic annulus were presented as boxplots using ANOVA to draw multiple group comparisons. AR was dichotomized into “no AR” and “moderate/severe AR” for logistic regression analyses. We constructed a model including all aortic root measurements. However, substantial multicollinearity between measures of aortic root was detected using the variance inflation factor (VIF). Therefore, we constructed separate models for all eight aortic root measurements. Age, sex, BSA, hypertension, and diabetes were pre-defined as relevant confounders and controlled for in all aortic root models. Results of logistic regression were corrected post-hoc using the Holm method and are depicted by odds ratios (OR) and corresponding 95% confidence intervals (CI). Differences were considered statistically significant at a two-sided p-value level of 0.05 after post-hoc correction. All statistical analyses were performed using R (version 3.6.2). A list of the used packages and versions can be found in the appendix.

Results

The analyzed study population included 8167 HCHS subjects of the first 10,000 HCHS participants, with 4191 female (51.3%) and a mean age of 62.23 ± 8.46 years (range 45–74 years) (Table 1; Fig. 1). 23 subjects were excluded due to moderate/severe AS and 69 due to bicuspid aortic valve morphology. While 7007 (85.8%) subjects were free of AR, 932 (11.4%) showed mild, 208 (2.5%) moderate and 20 (0.3%) severe AR. Patients with moderate or severe AR showed predominantly male sex, a higher age, and had more hypertension, CAD, atrial fibrillation, hypercholesterolemia, NT-proBNP elevation, and renal dysfunction compared with patients with no AR. Weight, height, heart rate, BSA, Glucose, triglycerides, hsCRP, hemoglobin, and diabetes did not show significant intergroup differences. The use of ACE inhibitors, angiotensin receptor blockers, beta-blockers, diuretics, and statins was more common in subjects with moderate/severe AR. Echocardiography revealed slightly lower left ventricular systolic function and larger left-sided cavities as well as a higher E/e’ ratio in subjects with moderate/severe AR compared to subjects without AR (Table 2). 7 subjects suffered from moderate/severe AR combined with mild AS. The prevalence of moderate/severe MR increased with AR severity.
Table 1

Baseline Characteristics of the study population stratified by AR severity

No AR (n = 7007)Mild AR (n = 932)Moderate/Severe AR (n = 228)p-value
Demographics and biological data
 Age, years61.6 ± 8.466.0 + 7.867.3 ± 7.4 < 0.001
 Male3369 (48.1)482 (51.7)125 (54.8)0.019
 Weight, kg78.6 ± 16.278.1 ± 15.377.5 ± 16.50.423
 Height, cm171.3 ± 9.5171.2 ± 9.3170.3 ± 9.90.359
 BSA, m21.9 ± 0.21.9 ± 0.21.9 ± 0.20.34
 Systolic blood pressure, mmHg138.4 ± 19.2140.9 ± 19.6143.5 ± 18.4 < 0.001
 Heart rate, bpm69.8 ± 11.269.1 ± 10.569.6 ± 11.90.208
 Current smoking1438 (20.6)114 (12.3)32 (14.1) < 0.001
 NYHA, II/III542 (8.6)84 (10.0)20 (10.5)0.267
Comorbidities
 Hypertension4292 (64.7)638 (70.3)171 (78.1) < 0.001
 Diabetes546 ( 8.5)68 ( 7.7)17 (7.9)0.728
 Coronary artery disease291 (5.9)45 (6.9)23 (14.9) < 0.001
 Atrial fibrillation341 (5.4)75 (8.9)28 (13.4) < 0.001
 Peripheral artery disease207 ( 3.2)41 ( 4.9)8 (4.1)0.042
 Medication
 Beta-blockers1114 (16.7)180 (20.0)51 (23.3)0.003
 Diuretics152 (2.3)28 (3.1)8 (3.7)0.15
 Statines1132 (17.0)182 (20.3)53 (24.2)0.002
 ACE/AT-I-antagonists1356 (20.4)207 (23.1)63 (28.8)0.003
Laboratories
 LDL, mg/dl121.0 [96.0, 146.0]118.0 [93.0, 143.0]119.0 [96.0, 150.0]0.058
 GFR, ml/min86.3 [75.5, 94.7]83.1 [71.9, 90.7]81.7 [71.4, 88.2] < 0.001
 NT-proBNP, ng/l77.0 [43.0, 141.0]100.0 [54.3, 179.5]136.0 [79.0, 228.0] < 0.001
 hsCRP,mg/l0.12 [0.06, 0.26]0.12 [0.06, 0.24]0.12 [0.06, 0.26]0.428
 Glucose, mg/dl92.0 [86.0, 100.0]92.0 [96.0, 99.0]93.0 [87.0, 100.0]0.562

Data are given as n (%) or mean ± standard deviation, p-value for intergroup differences

ACEi angiotensin-converting enzyme inhibitor, AR aortic regurgitation, ARB angiotensin receptor blocker, BMI body mass index, BSA body surface area, CAD coronary artery disease; hsCRP high sensitivity C-reactive protein, GFR glomerular filtration rate, NT-proBNP N-terminal pro-B-type natriuretic peptide, NYHA New York Heart Association

Fig. 1

Study flow-chart. From a total of 8259 subjects providing echocardiographic data, 92 were excluded due more than mild aortic stenosis or bicuspid aortic valve. Consequently, 8167 subjects were included in the study analysis. Of those, 1160 subjects suffered from aortic regurgitation. The aortic root was systematically measured in end-diastole and mid-systole and the correlation between aortic root dimensions and the severity of aortic regurgitation was calculated. AR aortic regurgitation, HCHS Hamburg City Health Study, TTE transthoracic echocardiography

Table 2

Echocardiographic findings of the study population stratified by AR severity

No AR (n = 7007)Mild AR (n = 932)Moderate/Severe AR (n = 228)p-value
Concomitant valvular disease
 Mild AS86 (1.3)23 (2.8)7 (3.4) < 0.001
 Moderate/severe MR189 (2.3)74 (7.9)19 (8.3) < 0.001
 Moderate/severe TR623 (8.9)193 (20.7)46 (20.2) < 0.001
Echocardiographic data
 LVEF 2D, %58.5 ± 5.258.3 + 5.057.6 ± 5.60.045
 LVEF 3D, %59.6 ± 6.859.2 ± 6.658.3 ± 6.80.178
 LVEDD, mm47.7 ± 5.247.9 ± 5.348.9 ± 6.40.004
 LVEDV, ml114.9 ± 31.8108.4 ± 30.6118.9 ± 34.6 < 0.001
 TAPSE, mm24.4 ± 4.323.8 ± 4.423.4 ± 4.20.001
 RV FAC, %43.2 ± 8.043.7 ± 7.742.7 ± 8.40.217
 IVSD, mm9.9 ± 1.710.3 ± 1.810.7 ± 1.9 < 0.001
 E/e ‘7.6 ± 2.17.8 ± 2.48.5 ± 2.9 < 0.001
 LAVI, ml/m227.5 ± 8.427.9 ± 8.930.2 ± 10.8 < 0.001
 LA Global Peak strain, %39.8 ± 14.438.5 ± 15.437.0 ± 14.50.014

Data are given as n (%) or mean ± standard deviation, p-value for intergroup differences. All subjects with moderate/severe aortic stenosis or bicuspid valves were excluded from the analysis

AS aortic stenosis, IVST interventricular septum thickness, LA left atrial, LAVI left atrial volume index, LVEDD left ventricular end-diastolic diameter, LVEDV left ventricular end-diastolic volume, LVEF left ventricular ejection fraction, MR mitral regurgitation, MS mitral stenosis, RV FAC right ventricular fractional area change, TAPSE tricuspid annular peak systolic excursion, TR tricuspid regurgitation

Baseline Characteristics of the study population stratified by AR severity Data are given as n (%) or mean ± standard deviation, p-value for intergroup differences ACEi angiotensin-converting enzyme inhibitor, AR aortic regurgitation, ARB angiotensin receptor blocker, BMI body mass index, BSA body surface area, CAD coronary artery disease; hsCRP high sensitivity C-reactive protein, GFR glomerular filtration rate, NT-proBNP N-terminal pro-B-type natriuretic peptide, NYHA New York Heart Association Study flow-chart. From a total of 8259 subjects providing echocardiographic data, 92 were excluded due more than mild aortic stenosis or bicuspid aortic valve. Consequently, 8167 subjects were included in the study analysis. Of those, 1160 subjects suffered from aortic regurgitation. The aortic root was systematically measured in end-diastole and mid-systole and the correlation between aortic root dimensions and the severity of aortic regurgitation was calculated. AR aortic regurgitation, HCHS Hamburg City Health Study, TTE transthoracic echocardiography Echocardiographic findings of the study population stratified by AR severity Data are given as n (%) or mean ± standard deviation, p-value for intergroup differences. All subjects with moderate/severe aortic stenosis or bicuspid valves were excluded from the analysis AS aortic stenosis, IVST interventricular septum thickness, LA left atrial, LAVI left atrial volume index, LVEDD left ventricular end-diastolic diameter, LVEDV left ventricular end-diastolic volume, LVEF left ventricular ejection fraction, MR mitral regurgitation, MS mitral stenosis, RV FAC right ventricular fractional area change, TAPSE tricuspid annular peak systolic excursion, TR tricuspid regurgitation Inter- and intraobserver reproducibility of echocardiographic aortic root assessment, derived from the measurements of a random sample of 100 exams measured by three different observers, were remarkably high for all variables, as shown by intraclass correlation coefficients ranging from 0.92 to 0.99 (Supplemental Table 1). Systolic were greater than diastolic measurements of the aortic root. Both the absolute and indexed diameters of aortic root components showed the lowest values in the no AR group and the highest values in the severe AR group (Table 3; Fig. 2). In binary logistic regression, age was significantly associated with AR prevalence (OR 1.08, 95% CI 1.06–1.10, p < 0.001). Furthermore, both in univariate as well as in multivariate logistic regression analysis, adjusted for age, sex, BSA, hypertension, and diabetes, significant associations were detected for all end-diastolic and mid-systolic aortic root variables with mild as well as with moderate/severe AR, even after correcting for multiple testing (Table 4, Supplementary Table 2, Fig. 3, Supplementary Fig. 1 and 2). The exclusion of subjects with mild AS did not change the reported associations with aortic root diameters (Supplementary Table 3). The strongest association for the correlation with moderate/severe AR was found for MS STJ (OR 1.33, 95% confidence interval 1.25–1.43, p < 0.001).
Table 3

Aortic root diameters absolute (mm) and indexed to body surface area (mm/m2) in relation to AR severity

None (n = 7007)Mild AR (n = 932)Moderate AR (n = 208)Severe AR (n = 20)p-value
Absolute
 ED Ao annulus20.33 ± 1.7120.65 ± 1.8420.50 + 2.0122.26 ± 1.91 < 0.001
 MS Ao annulus20.96 ± 1.7621.35 ± 1.8721.29 ± 1.9822.19 ± 1.85 < 0.001
 ED Ao sinus34.06 ± 3.8135.65 ± 4.1336.13 ± 4.7439.67 ± 4.61 < 0.001
 MS Ao sinus35.02 ± 3.8236.15 ± 4.1637.16 ± 4.6940.88 ± 3.68 < 0.001
 ED Ao STJ26.53 ± 3.0727.70 ± 3.2528.33 ± 3.6331.22 ± 3.27 < 0.001
 MS Ao STJ27.63 ± 3.2429.01 ± 3.6230.07 ± 3.8033.65 ± 3.81 < 0.001
 ED Asc Ao29.94 ± 3.7730.96 ± 4.1132.56 ± 4.6536.03 ± 3.43 < 0.001
 MS Asc Ao29.94 ± 3.5130.99 ± 3.8132.57 ± 4.1235.67 ± 3.37 < 0.001
Indexed to BSA
 ED Ao annulus10.79 ± 1.0910.97 ± 1.0811.03 ± 1.1512.18 ± 1.25 < 0.001
 MS Ao annulus11.09 ± 1.0811.32 ± 1.0511.35 ± 1.2012.00 ± 1.15 < 0.001
 ED Ao sinus18.01 ± 1.9918.86 ± 2.0619.18 ± 2.3821.39 ± 1.75 < 0.001
 MS Ao sinus18.54 ± 2.0419.23 ± 2.1019.69 ± 2.3822.30 ± 1.63 < 0.001
 ED Ao STJ14.03 ± 1.6614.68 ± 1.7714.99 ± 2.0016.75 ± 1.55 < 0.001
 MS Ao STJ14.65 ± 1.7315.42 ± 1.8415.98 ± 2.1018.28 ± 1.62 < 0.001
 ED Asc Ao15.79 ± 2.0816.40 ± 2.1717.10 ± 2.4219.56 ± 2.40 < 0.001
 MS Asc Ao15.82 ± 1.9616.48 ± 1.8917.26 ± 2.0419.41 ± 1.29 < 0.001

Data are given as mean ± standard deviation, p-value for intergroup differences

AR aortic regurgitation, Asc ascending, Ao Aortic/Aorta, BSA Body surface area, ED end-diastolic, MS mid-systolic, STJ sinotubular junction

Fig. 2

Correlation of AR severity with the sinotubular junction indexed to BSA as well as the ratio of sinotubular junction indexed and aortic annulus indexed to BSA. p-values for inter-group differences. Ao Ann Aortic annulus, BSA body surface area, STJ sinotubular junction

Table 4

Odds ratios and 95%-CIs derived from univariate and multivariate regression analysis for the associations of aortic root measurements with moderate/severe AR

UnivariateMultivariate
OR [95% CI]p-valueOR [95% CI]p-value
End-diastolic aortic root measurements
Ao Ann ED1.11 [1.02–1.21]0.0161.17 [1.05–1.32]0.013
 Age1.09 [1.06–1.11] < 0.001
 Male sex1.15 [0.72–1.85]1.000
 BSA0.21 [0.07–0.67]0.070
 Hypertension1.54 [1–2.42]0.331
 Diabetes0.89 [0.56–1.34]1.000
Ao Sinus ED1.16 [1.12–1.2] < 0.0011.19 [1.14–1.25] < 0.001
 Age1.07 [1.04–1.09] < 0.001
 Male sex0.81 [0.52–1.27]1.000
 BSA0.17 [0.06–0.46]0.006
 Hypertension1.76 [1.19–2.68]0.063
 Diabetes0.83 [0.53–1.22]1.000
Ao STJ ED1.24 [1.17–1.3] < 0.0011.26 [1.18–1.34] < 0.001
 Age1.08 [1.05–1.11] < 0.001
 Male sex0.93 [0.58–1.49]1.000
 BSA0.2 [0.06–0.62]0.049
 Hypertension1.5 [0.98–2.35]0.360
 Diabetes0.91 [0.57–1.38]1.000
Ao Asc ED1.2 [1.15–1.26] < 0.0011.2 [1.14–1.27] < 0.001
 Age1.07 [1.04–1.1] < 0.001
 Male sex0.86 [0.5–1.47]1.000
 BSA0.27 [0.07–1]0.206
 Hypertension1.68 [0.97–3.09]0.360
 Diabetes0.9 [0.52–1.45]1.000
Mid-systolic aortic root measurements
Ao Ann MS1.16 [1.07–1.26] < 0.0011.25 [1.11–1.4]0.002
 Age1.08 [1.05–1.1] < 0.001
 Male sex1.01 [0.65–1.55]1.000
 BSA0.26 [0.09–0.74]0.070
 Hypertension1.66 [1.12–2.54]0.132
 Diabetes0.85 [0.55–1.24]1.000
Ao Sinus MS1.17 [1.12–1.22] < 0.0011.2 [1.14–1.27] < 0.001
 Age1.08 [1.05–1.11] < 0.001
 Male sex0.74 [0.44–1.27]1.000
 BSA0.2 [0.06–0.68]0.070
 Hypertension1.71 [1.07–2.83]0.209
 Diabetes0.9 [0.53–1.41]1.000
Ao STJ MS1.26 [1.19–1.32] < 0.0011.33 [1.25–1.43] < 0.001
 Age1.08 [1.04–1.11] < 0.001
 Male sex0.57 [0.32–1.04]0.671
 BSA0.15 [0.04–0.61]0.070
 Hypertension2.01 [1.16–3.68]0.137
 Diabetes0.98 [0.54–1.62]1.000
Ao Asc MS1.23 [1.16–1.3] < 0.0011.26 [1.17–1.35] < 0.001
 Age1.08 [1.04–1.12] < 0.001
 Male sex0.73 [0.38–1.42]1.000
 BSA0.2 [0.04–1]0.206
 Hypertension1.4 [0.76–2.74]0.905
 Diabetes1.05 [0.52–1.89]1.000

P-values were corrected for multiple testing using the post-hoc Holm method

Ao aortic, AR aortic regurgitation, Asc ascending, BSA body surface area; CI confidence interval, ED end-diastolic, MS mid-systolic, OR odds ratio, STJ sinotubular junction

Fig. 3

Associations between aortic root dimensions and moderate/severe aortic regurgitation derived from multivariate logistic regression analysis. Odds ratios derived from multivariate logistic regression analysis adjusted for age, sex, body surface area, hypertension, and diabetes with Holm corrected p-values. Squares and horizontal lines represent odds ratios and 95% confidence intervals. Ao aortic, AR aortic regurgitation, Asc ascending, CI confidence interval, ED end-diastolic, MS mid-systolic, OR odds ratio, STJ sinotubular junction

Aortic root diameters absolute (mm) and indexed to body surface area (mm/m2) in relation to AR severity Data are given as mean ± standard deviation, p-value for intergroup differences AR aortic regurgitation, Asc ascending, Ao Aortic/Aorta, BSA Body surface area, ED end-diastolic, MS mid-systolic, STJ sinotubular junction Correlation of AR severity with the sinotubular junction indexed to BSA as well as the ratio of sinotubular junction indexed and aortic annulus indexed to BSA. p-values for inter-group differences. Ao Ann Aortic annulus, BSA body surface area, STJ sinotubular junction Odds ratios and 95%-CIs derived from univariate and multivariate regression analysis for the associations of aortic root measurements with moderate/severe AR P-values were corrected for multiple testing using the post-hoc Holm method Ao aortic, AR aortic regurgitation, Asc ascending, BSA body surface area; CI confidence interval, ED end-diastolic, MS mid-systolic, OR odds ratio, STJ sinotubular junction Associations between aortic root dimensions and moderate/severe aortic regurgitation derived from multivariate logistic regression analysis. Odds ratios derived from multivariate logistic regression analysis adjusted for age, sex, body surface area, hypertension, and diabetes with Holm corrected p-values. Squares and horizontal lines represent odds ratios and 95% confidence intervals. Ao aortic, AR aortic regurgitation, Asc ascending, CI confidence interval, ED end-diastolic, MS mid-systolic, OR odds ratio, STJ sinotubular junction

Discussion

The present study analyzes standardized, state-of-the-art echocardiographic aortic root measurements in association with the severity of aortic regurgitation in a large sample of the population-based HCHS. Major findings include that AR is common in the general population and that the size of all parts of the aortic root are associated with moderate/severe AR. Of the different aortic root parts, MS STJ size showed the strongest correlation with moderate/severe AR.

Prevalence of aortic regurgitation (AR)

The overall prevalence of AR in the population-based HCHS cohort, aged 45 to 74 years, was 14.2%, while the rate of moderate/severe AR was 2.8%. Subjects with moderate/severe AS or bicuspid valves were excluded from our analysis. Previously published studies on AR prevalence at the populational level reported very heterogeneous results [12-17]. AR prevalence ranged between 1 and 19%, depending on the baseline characteristics of the analyzed study cohort as well as on the methodology of echocardiographic evaluation. Most previously published studies demonstrated a significant association between age and AR prevalence [3, 13, 15]. While the overall prevalence of AR in younger populations is considerably low, it rises with ageing [3, 12, 13]. In line with this finding, we showed a significant association between age and AR prevalence. Furthermore, in several studies, including the Framingham Cohort Study, AR prevalence was associated with male sex [15, 18]. Nevertheless, other population-based studies did not find sex-associated differences in AR occurrence [3, 16, 17]. Our study showed in univariate analysis a significantly higher number of male subjects in the AR group, especially in those presenting with a moderate and severe AR. However, when controlling for age, BSA, and hypertension, this association did not remain statistically significant. Thus, the predominance of AR in male subjects might be primarily due to the higher prevalence of classical risk factors in males. Besides age and sex distribution, the improvement of echocardiographic technology might be causal for the relatively high AR prevalence in our study cohort since several of the mentioned studies are rather outdated. In particular, the high amount of mild AR cases might reflect a greater ability of current-era echocardiography equipment to detect small regurgitant jets. Furthermore, other comparable community based studies, as the OxVALVE Population Cohort Study (PCS), excluded subjects with known pre-existing valvular heart disease, resulting in a slightly lower rate of AR [19]. In summary, AR is a frequent finding at the populational-level, while its prevalence varies according to the analyzed study population and the utilized echocardiographic equipment.

Aortic root size and AR

In the present study, all mid-systolic and end-diastolic aortic root diameters were larger with increasing severity and prevalence of AR. A significant correlation between aortic root size and AR has been previously demonstrated by several research groups [1–3, 7, 16, 20]. The AV is mounted in the complex structure of the aortic annulus that is tightly integrated into the functional unit of the aortic root. Therefore, dilatation of the entire aortic root or of its separate components may result in AV annulus dysfunction and subsequent development of AR. However, previous studies focused predominantly on the aortic root as one entity, without analyzing the separate components or the timepoint of measurement within the cardiac cycle. Therefore, we aimed to address this issue by examining all integral aortic root parts in systole and diastole. In adjusted binary logistic regression analysis, all individual parts of the aortic root were associated with moderate/severe AR. Mid-systolic measurements showed a tendency towards a stronger correlation with AR when compared to end-diastolic measurements. According to current recommendations by the ASE and EACVI, end-diastole is the proposed timepoint for all aortic measurements, except the AoAn [9]. Still, limiting the assessment solely to end-diastolic measurements does not comply with the complex interplay of the aortic root with pressure changes during the cardiac cycle which ensures AV integrity. In this regard, our data suggest a correlation of the same magnitude between AR and mid-systolic as compared to end-diastolic aortic root diameters. This finding can be explained by the fact that HCHS participants were at moderate to advanced age and had a “normal” tricuspid AV. These selection criteria resulted in an exclusion of most subjects with a dilated AoAn, who frequently present at a young age (i.e., congenital connective tissue disorders) and those with congenital AV lesions (i.e., bicuspid AV). Previous data demonstrated that the age-dependent increase in diameter is more prevalent in STJ as compared to AoAn [21]. Therefore, the likely explanation for the strongest correlation between AR severity and STJ diameter is given by the fact that our middle-aged /older study cohort with tricuspid AV undergoes a progressive STJ dilatation due to ageing-dependent remodeling, while those subjects with primarily dilated AoAn are predominantly excluded. The functional impact of STJ dilatation on the prevalence and the severity of AR results from the radial displacement of AV commissures creating a central coaptation defect with consecutive AR. The normalization of STJ diameter by surgical STJ annuloplasty or replacement of the ascending aortic aneurysm corrects the commissural displacement and is followed by improved AV competence. Several previous studies focused on the definition of cut-off values of aortic root size which would be associated with AR occurrence [22]. Roman et al. and Seder et al. defined a threshold of 4.5 cm and 4.3 cm for the SoV diameter which were associated with a 100% prevalence of AR [1, 2]. Both studies used M-Mode echocardiography limiting the translation of these findings into the HCHS study design. Nonetheless, we were able to confirm and augment previous findings by demonstrating a linear correlation between aortic root dimensions and AR prevalence as well as an association between aortic root size and AR severity. However, due to the functional impact of several AV components on AV function and the development of AR (i.e., aortic cusps, AoAn, STJ) a simplified use of aortic root size to predict AR severity is rather counterproductive. The focus should rather be on the separate components of AV complex that determine AV function and their interaction.

Limitations

The results of this study are influenced by the subjects included. Our study cohort represents the first 10.000 subjects of the HCHS. Most of the subjects were middle-aged and free of symptoms of cardiovascular disease. Therefore, the translation into other populations and utilization in the clinical setting is limited. Only a small proportion of the overall cohort showed severe AR. Although our study is derived from a large sample, most subjects showed mild AR, which led to an underrepresentation of the moderate/severe group. The degree of association of the different aortic root components with AR severity could vary considerably according to patients’ baseline characteristics. The presented regression analysis was adjusted for all detectable confounding variables. Nevertheless, we cannot exclude that other relevant interacting variables were not considered. The pathogenetic mechanism by which STJ diameter is associated with AR was not addressed. Whether AR itself induced the aorta to dilate or aortic root dilatation led to regurgitation was not answered. Most importantly, our study was not designed to investigate the causality of AR, which is not possible due to cross-sectional study design, but to evaluate the correlation between aortic root diameters and AR severity.

Conclusion

In a large population-based sample, AR prevalence was 14.2%, with 2.8% being moderate/severe AR. Higher aortic root diameters at all levels were significantly associated with the prevalence and severity of AR. Of those, mid-systolic STJ had the strongest association with moderate/severe AR, reflecting its pathophysiological role in the context of an ageing aorta. Clinicians should closely monitor aortic root dilatation in the context of AR severity. Special focus should be paid to STJ dilatation as it showed the strongest association with a moderate/severe AR. Further validation in a broader, prospective population-based sample to evaluate the prognostic role of dilated aortic root diameters in the context of AR is needed. Below is the link to the electronic supplementary material. Supplementary file1 (DOCX 141 kb)
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Journal:  J Am Coll Cardiol       Date:  2000-08       Impact factor: 24.094

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Journal:  J Am Soc Echocardiogr       Date:  2015-02       Impact factor: 5.251

5.  Age-related prevalence of valvular regurgitation in normal subjects: a comprehensive color flow examination of 118 volunteers.

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6.  Aortic root dilatation as a cause of isolated, severe aortic regurgitation. Prevalence, clinical and echocardiographic patterns, and relation to left ventricular hypertrophy and function.

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Journal:  Ann Intern Med       Date:  1987-06       Impact factor: 25.391

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