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Left Atrial Remodeling is Associated with Left Ventricular Remodeling in Patients with Reperfused Acute Myocardial Infarction

Christodoulos E. Papadopoulos1*, Dimitrios G. Zioutas1, Panagiotis Charalambidis1, Aristi Boulbou1, Konstantinos Triantafyllou1, Konstantinos Baltoumas1, Haralambos I. Karvounis2 and Vassilios Vassilikos1

13rd Department of Cardiology, Hippokrateio University Hospital, Aristotle University of Thessaloniki, Greece

21st Department of Cardiology, AHEPA University Hospital, Aristotle University of Thessaloniki, Greece

*Address for Correspondence: CE Papadopoulos, Grigoriou E 11, 55236, Thessaloniki, Greece, Tel/fax: 0030 2310 223330; Email:

Dates: Submitted: 17 October 2016; Approved: 05 December 2016; Published: 07 December 2016

How to cite this article: Papadopoulos CE, Zioutas DG, Charalambidis P, Boulbou A, Triantafyllou K, et al. Left Atrial Remodeling is Associated with Left Ventricular Remodeling in Patients with Reperfused Acute Myocardial Infarction. J Cardiol Cardiovasc Med. 2016; 1: 001-008.

Copyright: © 2016 Papadopoulos et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Keywords: Left atrium; Remodeling; Myocardial infarction; Diastolic function; BNP


Background: Left atrial volume (LAV) has been established as a sensitive marker of left ventricular (LV) diastolic function and as an independent predictor of mortality in patients with acute myocardial infarction (AMI). LA remodeling and its determinants in the setting of AMI have not been much studied.

Methods: We studied 53 patients with anterior AMI and a relatively preserved LV systolic function, who underwent complete reperfusion and received guidelines guided antiremodeling drug management. LA and LV remodeling were assessed using 2D echocardiography at baseline and 6 months. LAV indexed for BSA (LAVi) was used as the index of LA size and further LA remodeling.

Results: LAVi increased signifi cantly at 6 months compared to baseline [28.1 (23.0-34.5) vs 24.4 (19.5- 31.6) ml/m2, p=0.002] following LV end diastolic-volume index change [56.8 (47.6-63.9) vs 49.5 (42.0-58.4) ml/m2, p=0.0003]. Other standard LV diastolic function indices did not show any signifi cant change. Univariateanalysis showed a strong positive correlation of LAVi change with BNP levels at discharge, LV mass index and LV volumes indices change, throughout the follow up period. Multivariate regression analysis revealed that BNP plasma levels was the most important independent predictor of LA remodeling (b-coef.=0.630, p=0.001).

Conclusions: Despite current antiremodeling strategies in patients with AMI, LA remodeling is frequently asssociated with LV remodeling. Additionally LAVi change in the mid-term reflects better than standard echocardiographic indices LV diastolic filling impairment.


There is increasing evidence that left atrial volume (LAV) is a more robust marker of cardiovascular events than LA area or diameter in subjects with sinus rhythm [1]. In more detail LAV has been strongly associated with mortality in high risk populations, such as patients with acute myocardial infarction [2-4], dilated cardiomyopathy [5], atrial arrhythmias [6] and in patients undergoing mitral valve surgery [7]. Furthermore LAV has been associated with the development of atrial fibrillation, ischemic stroke and heart failure [1,8,9] and is considered a stable indicator of LV diastolic dysfunction reflecting better its severity and chronicity [10].

Although LV remodeling has been well described as a potential complication of myocardial infarction (MI), LA remodeling has not been studied in detail [11]. The aim of the present study was to evaluate the prevalence of LA remodeling in patients with acute MI undergoing effective reperfusion and receiving up to date antiremodeling drug management.


The study was conducted at AHEPA University Hospital Cardiology Department and its protocol was approved by the Institutional Committee on human research. The study complied with the Declaration of Helsinki and all patients gave written inform consent before enrollment.

Sixty two consecutive patients were enrolled in the study. Patients were considered eligible if they presented with an acute anterior wall ST elevation MI, with a angiographically documented left anterior descending coronary artery stenosis (culprit lesion) and no history of cardiovascular disease. Acute MI was defined according to published guidelines [12]. All patients were successfully reperfused with either thrombolysis, primary percutaneous coronary intervention (PCI), thrombolysis followed by PCI within 24 hours of admission depending on the catheterization lab availability or coronary artery bypass grafting (CABG). Patients had to have TIMI flow grade III in LAD, following successful lysis or following PCI with stent deployment. Failure to achieve a TIMI flow grade III consisted an exclusion criterion. Additionally, patients that had significant coronary artery stenoses (lesion >70%) involving different myocardial wall territories and were left untreated, were excluded from the study population. Furthermore patients were excluded from the study if they had a poor echocardiographic image, any history of coronary heart disease, any history of terminal or systematic disease, any severe valve disease or cardiomyopathy or absence of sinus rhythm. During enrollment 16 patients with reperfused anterior wall STEMI were excluded from the study according to relevant inclusion and exclusion criteria. Ten patients had significant coronary artery stenoses that were left untreated by the interventionalist, 2 developed atrial fibrillation and 4 had inadequate echocardiographic images.

All patients received a complete antiremodeling and secondary prevention drug management including dual antiplatelet therapy, ACE inhibitors, b-blockers and statins where no contraindicated. Every effort was made in order to improve patients adherence to the recommended treatment.

Blood samples for measuring CPK MB levels, were taken on admission, then every 8 hours for the first day and subsequently every morning till discharge and peak value was reported. In addition B-type Natriuretic Peptide (BNP) levels at discharge were assessed using a commercially available immunofluoresence assay (BNP Triage, Biosite, San Diego).

All patients underwent a comprehensive transthoracic echocardiographic study using a GE Vingmed Vivid 7 system (GE Vingmed Ultrasound AS, Horten, Norway), at the day of discharge.

LV (end-systolic and end-diastolic) volumes and ejection fraction were estimated using Simpson’s modified biplane method and were further corrected for body surface area (end-systolic and end-diastolic volume index) [13]. The wall motion score index (WMSi) was obtained semiquantitatively using a 16-segment division of the LV [13]. LA volume was estimated using the biplane Simpson’s method from the apical 4 and 2 chamber views and was further corrected for body surface area to derive the LAV index (LAVi) [14]. To address the presence of LV hypertrophy LV mass index was assessed as previously described [15].

Pulsed Doppler echocardiography in order to assess standard LV diastolic filling velocities was performed using the apical 4-chamber view. Peak early filling velocity (E wave) and E wave deceleration time (DT) were recorded [16,17]. Color TDI was used to assess mitral annulus velocities. A 5-mm sample volume was placed at the apical 4-chamber view on the septal and lateral corner of the mitral annulus and the early diastolic velocity (e’) was recorded. The velocities obtained by the two different points of the mitral annulus were averaged. Furthermore the ratio of early transmitral filling velocity (E wave) to early diastolic mitral annulus velocity (LV E/e’ index) was calculated [18]. Finally propagation velocity was obtained and the ratio of E wave to propagation velocity was calculated (E/Vp) [19].

All echocardiographic measurements were obtained by a single experienced operator (C.E.P.) from three different cardiac cycles and were further averaged. All measurements were processed offline. The follow-up was undertaken at 6 months when a complete echocardiographic study was repeated.

Table 1: Study cohort characteristics (n=53).
Baseline demographics  
 Male (%) 46 (87)
Age 57±12
BSA (m2) 1.93±0.12
Dyslipaemia (%) 31 (59)
Hypertension (%) 28 (53)
Smoking (%) 34 (64)
Diabetes Mellitus (%) 13 (25)
CAD history (0%) 0 (0)
Time to initial reperfusion (min) 185±108
Primary PCI, n (%) 5 (9)
Thrombolysis+PCI, n (%) 42 (79)
Thrombolysis+CABG, n (%) 6 (12)
Coronary angiography data  
Coronary arteries involved 1.45±0.63
Left main artery disease, n (%) 13 (24)
Baseline ΤΙΜΙ flow 2±0.12
Post reperfusion ΤΙΜΙ flow 3
In Hospital Medical Treatment  
Aspirin, n (%) 52 (98)
Clopidogrel, n (%) 46 (86)
Beta blockers, n  (%) 52 (98)
ACE inhibitors, n (%) 46 (86)
Statins, n (%) 49 (92)
Nitrates, n (%) 30 (57)
Diuretics, n (%) 11 (21)
Antidiabetics, n (%) 10 (19)
Insulin, n (%) 1 (2)
IIb IIIa inhibitors, n (%) 10 (19)
Blood analysis  
Peak CK MB (IU/L) 211±184
BNP discharge (pg/ml) 562±787
Plus-minus values are mean ± SD
ACE inhibitors=Angiotensin converting enzyme inhibitors, CAD=coronary artery disease, CABG=coronary artery bypass grafting, PCI= percutaneous intervention, BNP=Brain Natriuretic peptide

Statistical analysis was performed with SPSS version 15.0 (SPSS Inc). A p-value less than 0.05 was considered statistically significant. Descriptive statistics for continuous variables are presented as median ± interquartile range and for nominal or ordinal variables as absolute frequencies and percentages. Descriptive statistics for the changes in LAVI and EDVI are also presented as mean ± 95% confidence interval, since they followed the normal distribution. Comparison of variables was done with the use the Wilcoxon signed ranks test (for continuous variables) and the McNemar test (for nominal or ordinal dichotomous variables), whichever was appropriate. Independent correlates of the LA volume index change throughout the follow-up were identified by their respective correlation coefficient. Variables significant at a p value of less than 0.01 were entered in the multivariate linear regression model and selection was based on the strength of correlation and its significance level.


From 62 patients initially enrolled in the study 53 consisted the study population. Eight were excluded due to poor echocardiographic images at follow up and one patient was lost to follow up. The baseline characteristics of the cohort are presented in Table 1. The population consisted mainly of middle aged males. Of note, there was a high prevalence of the five major cardiovascular risk factors. Nineteen patients had multivessel disease. Thrombolysis followed by PCI was the most commonly employed reperfusion therapy (79% of all patients) and the median time to reperfusion was 2.5 hours. TIMI III flow was evidenced in all patients except the ones treated with CABG where post surgery angiography was not performed due to ethical reasons.

Most patients received a combination therapy of the drugs used for secondary prevention showing significant adherence through follow-up period. Overall, 36 patients (78%) at baseline and 38 patients (83%) at follow-up were receiving an antiplatelet, a β-blocker, an ACE inhibitor, and a statin.

The echocardiographic variables at baseline and follow-up are presented in Table 2. All volumes assessed (LAVi, LVEDVi, LVESVi) increased significantly throughout the follow-up period. Indeed, LAVi showed a mean increase of 16.78% (95% CI for mean 7.95%-25.61%) and similarly LV EDVi a mean increase of 15.69% (95% CI for mean 5.63%-24.61%). Previous studies have used an increase in baseline LV end-diastolic volume >20% at follow-up as a cutoff value of major LV remodeling [16,20]. By using the same cutoff value for both LA (>20% increase in baseline LA volume) and LV (>20% increase in baseline LV end-diastolic volume) remodeling, we evidenced a significant prevalence of these geometric alterations, of 35% and 43% respectively. Interestingly patients who developed LA remodeling (>20% increase in baseline LA volume) had higher plasma BNP levels at baseline compared to patients without evidence of LA remodeling at follow-up (716±926 vs 312±404 pg/ml, p=0.005). Additionally we found that LA volume index at baseline was relatively high compared to the previously reported normal value for the general population (22±6 ml/m2) [21]. The proportion of patients with a LAVi larger than the 32 ml/m2 was 22% at baseline and 33% at follow-up. In terms of diastolic function assessment except LAVi, there was no change in the specific diastolic function indices that were assessed between baseline and follow-up (Table 2).

Univariate linear regression analysis was undertaken in order to highlight the variables that were associated with LA remodeling (any change in LAVi). As shown in Table 3, LV volumes, their net change throughout the follow-up period and LV hypertrophy (LV mass index) were positively correlated with LA remodeling, while baseline LV EF was negatively correlated. There was no association with any of the other LV diastolic indices tested. Finally there was a significant positive correlation with plasma BNP levels. Multivariate regression analysis revealed that BNP levels are the most significant predictor of LA remodeling in this specific cohort (Table 3).

Table 2: Echocardiographic variables at baseline and at follow-up.
Variable Baseline

6 month follow-up


LV remodeling
(>20% increase in EDVi)
  23 (43)  
LA remodeling
(>20% increase in LAVi)
  19 (35)  
LAVI (ml/m2) 24.4 (19.5-31.6) 28.1 (23.0-34.5) 0.002
LVESVi (ml/m2) 24.7 (20.6-31.3) 26.5 (19.9-37.4) 0.017
LVEDVi (ml/m2) 49.5 (42.0-58.4) 56.8 (47.6-63.9) 0.0003
LV Systolic function      
LVEF (%) 47.3 (39.2-57.0) 50.3 (39.2-56.7) ns
WMSi 1.68 (1.42-1.93) 1.43 (1.25-1.89) 0.006
LV Diastolic function      
E wave (cm/sec) 0.76 (0.68-0.95) 0.80 (0.65-0.98) ns
E/A 1.18 (0.83-1.38) 1.13 (0.73-1.35) ns
DT (msec) 236.5 (170.3 258.5) 237.5 (188.5 -263.5) ns
E/Em 17.4 (13.6-21.1) 16.2 (12.4-18.9) ns
E/Vp 1.48 (1.17-2.24) 1.46 (1.04-2.12) ns
Vp (cm/s) 50.0 (38.5-66.8) 51.0 (40.0-67.0) Ns
Values are median (interquartile range) or n (%) DT=E Wave Deceleration Time, E=E wave velocity, E/A=E to A wave velocity, E/Em=E wave velocity to mitral annulus early diastolic velocity ratio, E/Vp=E wave velocity to propagation velocity, LAVi=left atrial volume index, LVEDVi=left ventricular end-diastolic volume index, LVESVi=left ventricular end-systolic volume index, LVEF=left Ventricular Ejection Fraction, Vp=Propagation velocity, WMSi=Left Ventricular Wall Motion Score index
Table 3: Univariate and multivariate linear regression analysis for left atrial remodeling (R2 for the multivariate model was 0.727).
Variable (units) Univariate correlation coefficient p-value Multivariate beta coefficient p-value
Δ LV EDVi (ml/m2) 0.357 0.016 0.275 ns
Δ LV ESVi (ml/m2) 0.407 0.006 0.014 ns
LV EF (%) -0.386 0.009 -0.339 ns
Mass index (gr/m2) 0.322 0.03    
DT (msec) 0.189 0.220    
Em (cm/sec) -0.281 0.061    
BNP (pg/ml) 0.503 0.003 0.630 0.001
BNP= Brain Natriuretic Peptide, DT=E Wave Deceleration Time, Em=mitral annulus early diastolic velocity, LVEDVi=left ventricular end-diastolic volume index, LVESVi=left ventricular end-systolic volume index, LVEF=left Ventricular Ejection Fraction, Mass index=left ventricular mass index, WMSi=Left Ventricular Wall Motion Score index, Δ=net change throughout follow-up


The present study shows that despite the widespread use of reperfusion and antiremodeling drug strategy in patients with acute MI, LA remodeling following LV remodeling in patients with a relatively preserved LV systolic function, is a common sequale post MI. Furthermore we evidenced that in this specific population, LA volume was the only LV diastolic function index that was significantly impaired in the midterm and this LA remodeling process could be best predicted by BNP plasma levels at discharge.

Although the role of LA in the setting of acute MI has been well recognized from a long time ago [22], only the last decade LA volume has emerged as an independent predictor of mortality in this setting [2,3]. Additionally, LA enlargement has been proposed as a barometer of diastolic function and a predictor of common cardiovascular outcomes such as atrial fibrillation, stroke, congestive heart failure, and cardiovascular death in various clinic entities [2-9]. Therefore, enlargement of the LA reflects remodeling associated with serious pathophysiologic processes.

Doppler indices have been well studied and validated in AMI populations [16,18,19] and reflect filling pressures at the time of measurement. LA volume on the other hand represents the cumulative effects of filling pressures over time. Therefore, LA volume is regarded as a more stable parameter representing chronic LV diastolic function. Our study showed that in patients with a relatively preserved LV ejection fraction post AMI, between all standard LV diastolic function indices, LA volume was the only one that showed significant change in the midterm, supporting the concept that this index is a more real-life diastolic function index. In our study population LA volume index at baseline was relatively high compared to the previously reported normal value for the general population (22±6 ml/m2) [21]. This finding was probably the result of the relative high prevalence of arterial hypertension (53%) of the cohort, the population mean age (57±12) and LV hypertrophy.

Previous studies have evidenced the occurrence of LA remodeling and established the close relation between LA and LV remodeling following acute MI [11]. In the present study we documented a quite similar proportion of % change of LAVi and LVEDVi to follow-up, reflecting the similar natural history of these two different left chamber geometric alterarions. By using the cutoff value of 20% as described in the results section, we found a higher proportion of patients developing LV remodeling than LA remodeling (43 vs 35%). The main reason for that could be that despite the fact that increased LV filling pressures are the main mechanical driving forces for LA and LV remodeling, LV is additionally affected by direct myocardial injury and further ischemia. Furthermore LA usually needs more time to adapt to high LV filling pressures than LV, as evidenced in patients with mitral valve regurgitation. In contrast to our findings there are some reports, where no association between LA volume and further LV remodeling was found post MI and that might probably be due to the relative short follow-up period [23].

In the present study we evidenced that BNP plasma levels at baseline are the most significant independent predictor of LA remodeling in the midterm. BNP has been well recognized as an independent predictor of LV remodeling and other adverse cardiovascular events following acute MI [24-27]. Additionally this marker has been associated with various diastolic function indices reflecting LV filling pressure and has been shown to give incremental prognostic information in the same setting [28]. Although theoretically BNP levels would normally have some association with LA volume, as both indices are considered surrogates of LV diastolic filling properties, convincing data in the literature are missing. In contrast there are several reports where BNP levels are correlated with LA volume in various other clinical entities and especially patients with heart failure [29-31]. We have evidenced a strong positive association between LA remodeling and LV hypertrophy as expressed by LV mass index. It has been shown and we have published in the past similar results in such cohorts, documenting this strong association between LV hypertrophy and LV remodeling following an acute MI [26]. The present study establishes the correlation of LA remodeling with LV mass, reinforcing our concept that LA remodels together with LV and that the driving forces are quite the same.

The main limitation of the study was the small population, and our findings need to be replicated in larger cohorts. Another issue concerns the homogeneity of the cohort, as reperfusion treatment included lysis, PCI or CABG. It might be more appropriate to exclude CABG patients due to the fact that we have not angiographically documented graft patency post operation. In any case all patients had an anterior wall AMI with a relatively preserved LV systolic performance and received reperfusion with no evidence of any major adverse cardiovascular events through the follow-up time. This fact indirectly shows that probably there was no residual ischemia in the study population. Finally there is concern about the time (chronicity) of follow-up that might influence our results. There is no consensus about the exact period that LA needs to remodel following an acute MI, although many of the studies in the literature evaluating mainly LV remodeling have used the same 6 months period.

The clinical implications of our findings could be the increased awareness that physicians should show in patients with evidence of evolving LA remodeling on top of LV remodeling following an AMI. In this specific population up regulation of antiremodeling medication, increased adherence and close follow up with possible BNP plasma evaluation, might change the course of the disease. A prognostic assessment in this specific cohort, evaluating the impact of LA volume change on clinical endpoints, like major cardiovascular events or rehospitalizations would be interesting, although it is of no doubt that this study is underpowered to show any such association.

In conclusion, we have documented evidence that remodeling involves LA in addition to the LV chamber in a significant proportion of patients following an acute MI. Between other standard LV diastolic function indices, LA volume change stands as the only index that consistently deteriorates in the mid-term following an AMI and is strongly associated with BNP levels at discharge.


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