<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">WJCD</journal-id><journal-title-group><journal-title>World Journal of Cardiovascular Diseases</journal-title></journal-title-group><issn pub-type="epub">2164-5329</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/wjcd.2013.32A003</article-id><article-id pub-id-type="publisher-id">WJCD-30878</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  The assessment of atrial function by velocity-encoded magnetic resonance imaging
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>harles</surname><given-names>C. Vu</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>John</surname><given-names>F. Heitner</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Igor</surname><given-names>Klem</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Peter</surname><given-names>J. Cawley</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Anna</surname><given-names>Lisa C. Crowley</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Manesh</surname><given-names>R. Patel</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Jonathan</surname><given-names>W. Weinsaft</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Michele</surname><given-names>A. Parker</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Michael</surname><given-names>Elliott</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Robert</surname><given-names>M. Judd</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Raymond</surname><given-names>J. Kim</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Joseph</surname><given-names>C. Greenfield Jr.</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib></contrib-group><aff id="aff4"><addr-line>Division of Cardiology, University of Washington School of Medicine, Seattle, USA</addr-line></aff><aff id="aff2"><addr-line>Division of Cardiology, New York Methodist Hospital, Brooklyn, USA</addr-line></aff><aff id="aff3"><addr-line>Duke Cardiovascular Magnetic Resonance Center, Duke University Medical Center, Durham, USA</addr-line></aff><aff id="aff1"><addr-line>Stony Brook School of Medicine, Stony Brook, USA</addr-line></aff><aff id="aff5"><addr-line>Division of Cardiology, New York Presbyterian Hospital, Weill Cornell Medical Center, New York, USA</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>john.heitner@gmail.com(JFH)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>30</day><month>04</month><year>2013</year></pub-date><volume>03</volume><issue>02</issue><fpage>18</fpage><lpage>24</lpage><history><date date-type="received"><day>14</day>	<month>January</month>	<year>2013</year></date><date date-type="rev-recd"><day>13</day>	<month>March</month>	<year>2013</year>	</date><date date-type="accepted"><day>14</day>	<month>April</month>	<year>2013</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
   Introduction: The purpose of this study was to assess velocity-encoded cardiac magnetic resonance imaging (Ve-CMR) in a population of patients referred for cardiac magnetic resonance imaging (CMR), to determine the variability of atrial function, and to identify clinical parameters associated with left atrial function. Methods: This is a prospective study evaluating patients who were referred to our CMR center for a clinical CMR. Left atrial function was obtained via Ve-CMR thru-plane images across the mitral valve after acquiring 2 perpendicular in-plane images as “scouts”. The atrial function and mitral inflow were quantified by computer analysis (Argus, Siemens). Atrial function was defined as atrial contraction (A-wave) volume divided by total inflow volume. Left atrial volumes were calculated via computer analysis. Mitral regurgitation and left ventricular ejection fractions were assessed visually. Results: Thirty-nine patients, with mean age 56 +/- 10 years, were enrolled. The mean left atrial function was 22.9% +/-14.5%; the range in left atrial function was 0% - 57%. There was a significant positive correlation between atrial function and increased left ventricular ejection fraction (r = 0.44, P &lt; 0.01). There was a significant negative correlation between atrial function and severity of mitral regurgitation (r = -0.60, P &lt; 0.01), as well as left atrial volume (r = -0.36, P = 0.02). Conclusion: Our results indicate a wide variability in left atrial function and a significant association between left atrial function and left ventricular ejection fraction, left atrial volume and mitral regurgitation. 
 
</p></abstract><kwd-group><kwd>Atrial Function; Velocity-Encoded; Cardiovascular Magnetic Resonance</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. INTRODUCTION</title><p>Atrial function is an important parameter in cardiac hemodynamics contributing significantly to left ventricular (LV) function [<xref ref-type="bibr" rid="scirp.30878-ref1">1</xref>]. Combined two-dimensional and Doppler echocardiography is the most widely used modality to assess the contribution of atrial systole to ventricular filling; two other less utilized modalities include ultrafast computed tomography and radionuclide angiography [2- 5].</p><p>Cardiac magnetic resonance imaging (CMR) is a relatively new and emerging imaging modality that can be used to assess left atrial function. Early CMR methods have used volume assessments via cine-CMR for the assessment of left atrial function [<xref ref-type="bibr" rid="scirp.30878-ref6">6</xref>]. Velocity-encoded magnetic resonance imaging (Ve-CMR) is a technique that can measure both the velocity and the quantity of blood flow through the mitral valve during diastole, and thus can be used to quantify left atrial function. Due to its excellent spatial resolution, Ve-CMR can measure the passive early diastolic flow and the contribution of atrial systole to both left and right ventricular diastolic filling in normal subjects [7-10].</p><p>Previous studies using Ve-CMR have assessed left atrial function in small populations with either valvular stenosis or normal hearts [8,9]. This study is designed to assess this technique in a population of patients with a variety of indications for CMR, to determine the variability of atrial function within this population, and to assess the clinical variables associated with left atrial function.</p></sec><sec id="s2"><title>2. METHODS</title><sec id="s2_1"><title>2.1. Ethics Statement</title><p>At the time of the CMR study, written consent was obtained from all study participants and the institutional review board of Duke University Medical Center approved the study protocol. This study was in compliance with Health Insurance Portability and Accountability Act (HIPAA) guidelines.</p></sec><sec id="s2_2"><title>2.2. Patients</title><p>The study group consisted of 39 prospectively enrolled patients. All patients were referred for a CMR study for the evaluation of myocardial viability, left ventricular systolic function assessment, or for an abnormal echocardiogram. Exclusion criteria were contraindications to CMR (e.g. size greater than the magnet bore, pregnancy, vascular clips, pacemakers, defibrillators, claustrophobia). All patients had a comprehensive history obtained at the time of their CMR study.</p></sec><sec id="s2_3"><title>2.3. CMR</title><p>All scans were performed on a 1.5-Tesla scanner with a phased-array receiver coil (Siemens Sonata). Longand short-axis scout images were used to determine the double-oblique longand short-axis views.</p><p>Steady-state free-precession cine images were taken in three long-axis views, as well as in short-axis views of the entire left ventricle (slice thickness—6 mm; gap between slices—4 mm). Typical parameters used were: repetition time 3.0 ms; echo time 1.5 ms; flip angle 25˚; temporal resolution 35 ms/phase; in-plane resolution 1.7 &#215; 1.4 mm.</p><p>A velocity-encoded gradient echo sequence was used to acquire in-plane phase-contrast and magnitude images in 2-chamber and 4-chamber long-axis views at the mitral annulus. Using these in-plane images as “scout images”, through-plane images across the mitral valve were then taken (<xref ref-type="fig" rid="fig1">Figure 1</xref>). Typical parameters were: FOV 320 mm; slice thickness 6 mm; flip angle 25˚; in-plane resolution 2.1 &#215; 1.4 mm; temporal resolution 60 ms/ phase interpolated to 30 ms/phase; echo time 3.0 ms. Retrospective electrocardiogram gating was used. The typical VENC was between 80 and 120 cm/second.</p><p>Flow analysis was performed on the through-plane VeCMR phase-contrast and magnitude images acquired across the mitral valve. To determine blood flow and volume, region of interest (ROI) curves on the Ve-CMR phase-contrast images were drawn, with subsequent im-</p><p>age analysis by commercial software (Argus, Siemens).</p></sec><sec id="s2_4"><title>2.4. Left Atrial Function</title><p>Using the flow-time curve, the beginning and ending times of the E-wave (passive ventricular filling) and Awave (atrial contraction) were determined. The inflow volumes from passive ventricular filling and atrial contraction were calculated from the corresponding net flowtime curves (<xref ref-type="fig" rid="fig2">Figure 2</xref>). Left atrial function was defined as the atrial contraction volume divided by the total inflow volume.</p></sec><sec id="s2_5"><title>2.5. Other Cardiac Parameters</title><p>Left ventricular wall thickness (anterior and posterior), end-diastolic diameter, and end-systolic diameter were measured from the mid-chamber cine short-axis view. Image analysis was done using commercial software (Argus, Siemens), with left ventricular ejection fraction being visually estimated by an experienced physician. PR interval and RR interval were calculated from the electrocardiogram.</p><p>Because quantitative evaluation of mitral regurgitation is not reliable, for each patient, the degree of mitral regurgitation was evaluated qualitatively from the cine MR images [<xref ref-type="bibr" rid="scirp.30878-ref11">11</xref>]. A mitral regurgitation score was assigned for each patient according to the following table: None = 0, Trivial = 1, Mild = 2, Moderate = 3, Severe = 4.</p><p>Lengths and widths of the left atrium were measured in the two-chamber and four-chamber cine views (equivalent to the apical two-chamber and apical long-axis imaging planes on echocardiogram, respectively). In addi-</p><p>tion, height was measured in the three-chamber cine view (equivalent to the parasternal long-axis on echocardiogram). Left atrial volume was calculated by modeling the left atrium as a prolate ellipsoid:</p><disp-formula id="scirp.30878-formula77597"><label>(1)</label><graphic position="anchor" xlink:href="3-1910162\c2096005-f1ab-494f-a79a-b929109fb9fe.jpg"  xlink:type="simple"/></disp-formula><p>where V<sub>1</sub> = three-chamber view height, V<sub>2</sub> = fourchamber view width and V<sub>3</sub> = four-chamber view length [<xref ref-type="bibr" rid="scirp.30878-ref12">12</xref>].</p></sec><sec id="s2_6"><title>2.6. Statistical Analysis</title><p>Continuous data are stated as mean +/− standard deviation. Comparisons between groups were computed using 2-sample t-tests. Standard linear regression analysis was used to compare left atrial function and other cardiac parameters; all stated correlations are Pearson correlation coefficients. All statistical tests are two-tailed, with P &lt; 0.05 considered statistically significant.</p></sec></sec><sec id="s3"><title>3. RESULTS</title><p>All patients had a complete CMR test. The mean age was 56 +/− 10 years, the study group was 46% female, and mean body mass index was 28.5 +/− 5.2 kg/m<sup>2</sup>. Fiftynine percent (23/39) of the study group had a history of hypertension and approximately 40% (16/39) of the population had diabetes mellitus and left ventricular hypertrophy. <xref ref-type="table" rid="table1">Table 1</xref> lists the baseline characteristics of the study group.</p><p>Mean left atrial function was 22.9% +/− 14.5%; the</p><p><xref ref-type="table" rid="table1">Table 1</xref>. Baseline characteristics of study group.</p><p><img src="3-1910162\53cf569f-ec5a-4179-8754-23bb9b42370f.jpg" /></p><p>CAD: coronary artery disease, BMI: body mass index, CHF: congestive heart failure.</p><p>range in left atrial function was 0% - 57%. <xref ref-type="table" rid="table2">Table 2</xref> presents the mean values of several cardiac parameters and their correlation with left atrial function. The mean left ventricular ejection fraction was 58% +/− 12%; there was a significant positive correlation between atrial function and left ventricular ejection fraction (r = 0.44, P &lt; 0.01). The mean mitral regurgitation score was 1.1 +/− 1.0; atrial function was inversely correlated with severity of mitral regurgitation (r = −0.60, P &lt; 0.01). In addition, mean left atrial volume was 52.4 +/− 40.0 cm<sup>3</sup>; higher left atrial volume was associated with lower left atrial function (r = −0.36, P = 0.02). The mean PR interval was 167 +/− 30 ms; no significant correlation was found between PR interval and left atrial function (r = 0.03, P = 0.87).</p><p>There were two patients with atrial fibrillation and one patient with complete heart block that were confirmed to have no atrial contraction and therefore zero left atrial function. Four additional patients had zero left atrial function despite having normal sinus rhythm on electrocardiogram and no history of arrhythmias. Of these four patients, none had severely reduced left ventricular ejection fraction. Three of these patients had diabetes, three had left ventricular hypertrophy, and two had history of hypertension. In addition, these patients had trivial or mild mitral regurgitation and normal PR intervals, except for one patient who had the longest PR interval (231 ms) of any patient in the study group. In addition, one patient reported a history of palpitations. The baseline characteristics and cardiac parameters of these four patients are listed in <xref ref-type="table" rid="table3">Table 3</xref>.</p></sec><sec id="s4"><title>4. DISCUSSION</title><p>The results of this study are consistent with previously</p><p><xref ref-type="table" rid="table2">Table 2</xref>. Cardiac parameters and correlation to left atrial function.</p><p><img src="3-1910162\6df387be-7eb6-4ed6-ab94-a03c13a6268f.jpg" /></p><p>LV: left ventricular, SD: standard deviation, R: correlation coefficient.</p><p><xref ref-type="table" rid="table3">Table 3</xref>. Patients with zero left atrial function with normal sinus rhythm and no history of arrhythmias.</p><p><img src="3-1910162\e5802342-f245-4be9-be2e-c354f989bbe5.jpg" /></p><p>CAD: coronary artery disease, LV: left ventricular.</p><p>reported results, including those using Ve-CMR, echocardiography, and invasive techniques (<xref ref-type="table" rid="table4">Table 4</xref>). However, our study group had a greater variability in atrial function than all of these prior studies. We postulate this to be due to the variety of clinical indications in our study group (referral population), compared to prior studies with either normal patients or patients with a specific pathology. Previous studies indicate a wide variability in left atrial function for patients with different disease states: for example, mean left atrial function in patients with severe mitral stenosis was found to be 9 +/− 5%, while mean left atrial function in patients with myocardial infarction to be 42 +/− 12% [13,14]. Our study confirms that left atrial function can vary significantly within a clinical referral population.</p><p>Matsuda (1983) found an association between left ventricular ejection fraction and left atrial work (defined as atrial contraction volume); this correlation was attributed to the Frank-Starling law operating in the left atrium [<xref ref-type="bibr" rid="scirp.30878-ref14">14</xref>]. We postulate that the Frank-Starling law can explain the correlation between left atrial function and left ventricular ejection fraction found in this study: increased left atrial function leads to increased left ventricular enddiastolic volume, which would lead to increased left ventricular contractility and thus increased left ventricular ejection fraction.</p><p>The inverse correlation between left atrial volume and left atrial function may be due to increased passive left ventricular filling: increased left atrial volume would create an increased pressure gradient between the left atrium and left ventricle, which would lead to increased passive ventricular filling (E-wave), thereby decreasing the calculated left atrial function. Similarly, increased mitral regurgitation would lead to increased left atrial volume, thereby increasing passive ventricular filling and thus decreasing left atrial function; it has been shown that increased mitral regurgitation is correlated with increased peak E-wave velocity [<xref ref-type="bibr" rid="scirp.30878-ref15">15</xref>].</p><p>As detailed in the Results section, there were four patients that had zero left atrial function (absent A-wave) despite having normal sinus rhythm on ECG. Absent atrial function has been shown in patients with restrictive cardiomyopathy, such as amyloidosis [<xref ref-type="bibr" rid="scirp.30878-ref16">16</xref>], and pericardial constriction [<xref ref-type="bibr" rid="scirp.30878-ref17">17</xref>]. However, given that three of these patients had a history of LVH, we believe that a restricttive physiology (i.e. left ventricular hypertrophy leads to decreased left ventricular compliance, leading to impaired active filling) most likely explains these patients’ zero left atrial function. Alternatively, it is possible that these patients may have had atrial fibrillation but recently spontaneously converted back into normal sinus rhythm, as there can be a delay of up to several weeks for recovery of mechanical function after normal electrical function has been restored [<xref ref-type="bibr" rid="scirp.30878-ref18">18</xref>]. One patient did have a history of palpitations and therefore possibly had undiagnosed paroxysmal atrial fibrillation. Finally, one patient’s atrial function may be explained by possible E/A fusion from a markedly prolonged PR interval.</p><p>Limitations to this study include the lack of correction for mitral valve annulus motion, which may lead to calculation errors [<xref ref-type="bibr" rid="scirp.30878-ref19">19</xref>]. In addition, this study had a relatively small sample size. However, to our knowledge, this study is larger than any previous study using VeCMR to examine atrial contribution to left ventricular filling. By successfully evaluating left atrial function for 39 patients referred to CMR for a multitude of clinical indications, we have demonstrated that Ve-CMR can</p><p><xref ref-type="table" rid="table4">Table 4</xref>. Comparison of results with prior studies of left atrial function.</p><p><img src="3-1910162\c038fc15-1159-42da-9a8c-d23cef75c695.jpg" /></p><p>Ve-CMR = velocity-encoded cardiac magnetic resonance: TEE = transesophageal echocardiography.</p><p>evaluate left atrial function on a wide variety of patients.</p></sec><sec id="s5"><title>5. CONCLUSION</title><p>In this population of patients referred for a clinical CMR, there is a wide variability in left atrial function. Left atrial function is significantly associated with left ventricular ejection fraction, left atrial size, and mitral regurgitation.</p></sec><sec id="s6"><title>REFERENCES</title></sec><sec id="s7"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.30878-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Braunwald, E. and Frahm, C.J. (1961) Studies on Starling’s law of the heart: IV. Observations on the hemodynamic functions of the left atrium in man. 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