Background

Left atrial (LA) enlargement is frequently the default clinical hallmark of structural remodeling in response to LA pressure and volume overload [1]. Blood pressure (BP) has been a crucial determining factor of LA enlargement [2]. Conventional single BP measurement cannot reflect the patient’s intrinsic BP characteristics because of insufficient sampling and the probability of falsely higher reading due to emotional factors, such as the white coat impact [3].

A complementary method is Ambulatory Blood Pressure Monitoring (ABPM), which permits various measurements under more controlled and consistent conditions. Additionally, various BP measurements offer data about variability. Augmented nighttime BP variability (BPV) was associated with atherosclerosis and consequent stroke [3, 4]. The higher nighttime BP and its variability are independently related to LA enlargement [5]. The LA enlargement is a subclinical deviation that conveys a more significant stroke hazard [6].

Asymptomatic paroxysmal atrial fibrillation (AF) has been claimed to cause a cryptogenic stroke [7]. Loss of LA longitudinal deformation, decreased LAEF, and other structural LA remodeling and electrophysiological parameters were related to an augmented risk of paroxysmal AF in patients with cryptogenic stroke [8, 9].

Intensive intervention for these patients may delay LA remodeling progression and reduce the risk of ischemic stroke. However, the association between BPV and LA enlargement has not been addressed in patients with cryptogenic stroke. The current study aimed to evaluate the influence of BPV as a risk factor for cryptogenic stroke and to test the relation between BPV and LA remodeling in these patients, which could be used as a clue to add ABPM to their workup.

Methods

This prospective, cross-sectional cohort study was performed from September 2019 to November 2021. The local research committees approved the study following the Declaration of Helsinki. We acquired informed written consent from all the participants. We included 108 consecutive patients with cryptogenic ischemic stroke (Group I). The stroke unit referred them for cardiac evaluation after suffering from a cerebral stroke.

We defined cryptogenic stroke as any ischemic stroke without apparent cause despite extensive history and corresponding studies. We subjected all the patients to a detailed history, including preceding events, such as recent invasive procedures, intravenous drug abuse, and recent pregnancy. We focused on atherosclerotic risk factors, including hypertension, dyslipidemia, and diabetes mellitus (DM). We reviewed the family history of premature atherosclerotic disease, cerebrovascular stroke (CVS), or sudden death. Then, we subjected all the patients to a detailed physical examination.

The cardiac evaluation included a 12-lead electrocardiogram (ECG), ambulatory 24 h ECG to exclude AF, ABPM, transthoracic, and transesophageal echocardiography (TEE) to exclude a thrombus, cardiac mass, vegetation, and intracardiac shunt. We performed non-contrast CT brain, carotid ultrasound, transcranial Doppler, MRI brain, and CT angiography of the head and neck for all the patients to exclude patients with any apparent cause of stroke. We outlined the evaluation plan for cryptogenic stroke in Fig. 1.

Fig. 1
figure 1

Workup for patients with cryptogenic stroke

All the included patients had sinus rhythm at the examination and left ventricular ejection fraction (LVEF) over 50%. According to the European Society of Echocardiography, we evaluated cardiac chamber size, LVEF, and LA dimensions [10]. We measured LV end-diastolic indexed volume (mL/m2) and LV end-systolic indexed volume (mL/m2) and also peak velocity of E and A waves of mitral flow, é wave was measured from the apical four-chamber view, with 2–5 mm sample volume taken from the septal corner of the mitral annulus, and E/é ratio was calculated.

We obtained the 2D volume of the LA from the apical view during a short breath-hold. We acquired 2D LA images from apical four- and two-chamber views. In 2D, we assessed the LA area on the four-chamber view in end systole. We measured volumes using the biplane modified Simpson’s method. We indexed LA volumes to the body surface area. We measured the maximal LA volume index (Max LAVI) at the ventricular end-systolic frame just before the mitral valve opening from the apical views. We measured minimal LA volume (Min LAVI) at the end of LV diastole, just before the mitral valve closure. We calculated the LA function with the following formula: LA ejection fraction (LAEF): (Max LAVI-Min LAVI)/Max LAVI × 100.

We excluded patients with atrial flutter and fibrillation, bundle branch block, poor acoustic window, and a history of coronary artery disease (CAD). Also, we excluded patients with previous percutaneous coronary intervention (PCI) or open-heart surgery, previous ablation procedure, pulmonary hypertension, and left ventricular hypertrophy (LVH). The ECG assessment included P-wave amplitude, QRS duration, and QT interval.

We performed a routine laboratory test, including the lipid profile and blood glucose level. We defined DM as a fasting plasma glucose > 140 mg/dl or the use of antidiabetic drugs. We described obesity as body mass index (BMI) ≥ 30 kg/m2. We defined hypertension according to the European Society of Cardiology Guidelines as systolic BP (SBP) ≥ 140 mmHg or diastolic BP (DBP) ≥ 90 mmHg [11]. We defined ABPM limits above the normal if the mean 24 h SBP was > 130 or DBP ≥ 80, the daytime was ≥ 135/ ≥ 85 mmHg, or the nighttime was ≥ 120/ ≥ 70 [12].

We defined hypercholesterolemia as total serum cholesterol > 220 mg/dl or the use of lipid-lowering medications. We informed the patients that cuff inflation might be associated with some distress. We used an ABPM device validated against accepted universal criteria, CONTEC 50, for all the patients. The data included all daytime and nighttime BP readings with an indication of normal BP, average SBP, DBP, and heart rate, time‐weighted average SBP, DBP, and heart rate for the 24 h, daytime, and nighttime, with standard deviations (SD) and the number of accurate BP readings, the percentage decline in nocturnal SBP and DBP. We used the non‐dominant upper limb for measurements and used a suitable cuff. We set the device to obtain BP readings every 15 min during the daytime (06:00–23:00 h) and every thirty minutes at night (23:00–06:00 h). Then, we confirmed that ≥ 70% of the expected 24‐h readings were valid and registered the ABPM data during regular workdays. We used the SD indices for the assessment of the short-term BPV.

Group II included 100 consecutive individuals who attended echocardiographic units without any history of cerebrovascular insult, cardiac ablation procedure, or overt structural heart disease (the same echocardiographic exclusion criteria as Group I). All were subjected to ABPM and echocardiographic measurements like patients in Group I.

Statistical analysis

We analyzed the data using the Statistical Program for Social Science (SPSS) version 20.0. We expressed the quantitative data as mean ± SD. We described the qualitative data as frequency and percentage. We used the Kolmogorov–Smirnov test to analyze the normal distribution of continuous data, which was normally distributed.

We used an independent-samples t test of significance to compare the two means. We compared the means of age, 24H systolic SD, day systolic SD, night systolic SD, 24H diastolic SD, day diastolic SD, night diastolic SD, LVESVI mL/m2, LVEDVI mL/m2, Min LAVI mL/m2, Max LAVI mL/m2, and LA EF %.

We applied the chi-square (X2) test of significance to evaluate proportions between two qualitative parameters (risk factors and medications).

We used Pearson’s correlation coefficient (r) to test the LA remodeling parameters and their quantitative predictors. We used Spearman’s correlation coefficient (r) test for correlating the LA remodeling parameters and their qualitative predictors. We used the logistic multivariate regression analysis to study the multiple variables that may affect the LA remodeling parameters and to adjust the different potential confounders, including the basal demographic characteristics and the ABPM parameters. We presented the adjusted odds ratio with 95% confidence intervals.

We calculated the sample size and the power analysis using g*power software 3.1.9.4. We used the sample size calculation criteria: 95% confidence limit and 80% study power for different variables, and we found it at 100 patients. The cutoff point of statistical significance was 0.05.

We assessed intra-observer and inter-observer variability for echocardiographic parameters by randomly selecting 15 patients and repeating the analysis on the same cine loop by the same investigator or independently by two separate investigators using intraclass correlation coefficients (ICC) with values less than 0.5 indicating poor reliability, between 0.5 and 0.75 mean moderate reliability, between 0.75 and 0.9 mean good reliability, and above 0.9 excellent reliability.

Reproducibility

Intra-observer and inter-observer variability for echocardiographic parameters ranged from 0.91 and 0.95.

Results

Our two-center comparative cross-sectional study included 108 consecutive patients with cryptogenic stroke in Group I and 100 patients without stroke in Group II. We found no significant difference between both groups regarding the basal demographic characteristics, risk factors, and antihypertensive medications, as shown in Tables 1 and 2.

Table 1 Comparing demographic characteristics of the study population
Table 2 Comparing antihypertensive medication of the study population

In the cryptogenic group, 9.2% (n = 10) of patients had palpitation despite that ambulatory ECG monitoring did not detect any arrhythmias.

Moreover, there were no statistically significant variances between both groups in the left ventricular volumes ( LVESVI and LVEDVI), with P values of (0.867 and 0.956), respectively. There were no significant differences in the parameters that assess LV filling pressure and diastolic functions (peak E velocity, peak A velocity, and E/é ratio) with P values of (0.781, 0.926, and 0.409), respectively, as shown in Table 3.

Table 3 Comparing echocardiographic parameters and BPV parameters in both groups

While, regarding LA and BPV parameters, patients with cryptogenic stroke (Group I) had significantly higher Min LAVI and Max LAVI than Group II, with a P value of 0.001 for both parameters, simultaneously, patients with cryptogenic stroke had significantly lower LA EF, with a P value of 0.008, as shown in Table 3.

Also, patients with cryptogenic stroke had higher BPV as measured by SD parameters than Group II, with a P value of 0.001 for all SD parameters, as shown in Table 3.

We correlated the LA remodeling parameters to the different potential confounders, as shown in Tables 4 and 5. We found that aging and all BPV parameters, as measured by SD, were positively correlated with the (Min LAVI, Max LAVI). In contrast, both aging and BPV parameters were correlated negatively with the LA EF; this occurred in both groups. Finally, in cryptogenic stroke patients, we found a negative correlation between the E/é ratio and LA EF with a P value of 0.018.

Table 4 Correlation between echocardiographic parameters and the demographic data in Group I
Table 5 Correlation between echocardiographic parameters and the demographic data in Group II

We did a logistic multivariate regression analysis for the covariant. It was significantly correlated with the LA remodeling parameters (Min LAVI, Max LAVI, and LA EF). After adjusting all variables, age, night systolic SD, and night diastolic SD parameters were independent predictors of LA remodeling, as shown in Table 6.

Table 6 Multivariate regression analysis for covariants affecting the LA remodeling parameters

These results could propose that high BPV in patients with cryptogenic stroke may lead to abnormal LA remodeling and function, which may be a substrate for occult AF, the source of stroke in these patients.

Discussion

Stroke was the fifth principal reason for death, and cryptogenic stroke represents 15–40% of ischemic strokes in different studies [13]. The recent guidelines do not make specific recommendations to prevent cryptogenic stroke [14].

In our study, the high BPV was associated with structural and functional LA remodeling. Moreover, structural and functional LA remodeling was more prevalent in patients with cryptogenic stroke. Consequently, the high BPV may lead to LA structural and functional changes and an increased risk of cryptogenic stroke. The results were similar to Vural MG et al. [15], who found a relation between LA remodeling and cryptogenic stroke in young patients.

LA remodeling denotes the spectrum of pathophysiological alterations in the LA mechanical and electrical function that respond to stress disorders such as hypertension, heart failure, DM, and obesity. Structural LA remodeling often responds to LA pressure and volume overload [1, 16].

Remodeling is primarily adaptive, but it often becomes maladaptive in response to a chronic pathological provocation, and it is linked with an enhanced probability of cardiovascular morbidity and mortality [16]. In our study, we focused on mechanical remodeling.

We used Min LAVI, Max LAVI, and LA EF to study maladaptive mechanical remodeling. We found that patients with cryptogenic stroke had statistically significantly lower LA EF than Group II. Chinali M et al. [17] studied about 2800 patients with a high prevalence of obesity, DM, and LA systolic dysfunction and found a higher rate of cardiovascular events.

Some studies found that reduced LA EF was associated with increased pressure in the LA appendage and abnormal LA strain. This strain may be a substrate for thromboembolism [15, 18].

Norioka et al. [5] studied the impact of BPV on LA function and structure in 140 patients with paroxysmal AF and normal EF. They concluded that higher nighttime BP and its variability were associated with LA enlargement, and nighttime BP and its variability have additional predictive value for LA remodeling. Moreover, Doménech et al. found that nighttime BP was associated with LA size and the release of natriuretic peptides in patients with idiopathic AF [19].

High BPV was strongly associated with LA remodeling and reduced LA EF in our study. So, more intensive investigation and more careful evaluation may be required for patients with cryptogenic stroke who have LA remodeling, which may be a clue for high BPV or a substrate for occult atrial fibrillation with increased risk of stroke in our study. 9.2% of patients in the cryptogenic group had symptoms of palpitation despite that Holter monitoring did not diagnose any arrhythmias.

The limitations of this study include the relatively small number of patients. Also, both left atrial volumes and LA EF are affected by multiple factors.

Conclusions

The patients with cryptogenic stroke had higher short-term BPV as measured by SD. Also, the patients with cryptogenic stroke had higher Min LAVI, Max LAVI, and lower LA EF. LA remodeling may be a substrate for paroxysmal AF and subsequent thrombo-embolization, and these patients may require heart rate monitoring for a more extended period to detect arrhythmias. Also, the presence of left atrial remodeling in echocardiographic screening for patients with cryptogenic stroke may be a clue to adding the APBM to the workup. Tackling BPV may be of value for both primary and secondary preventions of cryptogenic stroke.