Abstract
Background and Purpose
Left ventricular (LV) diastolic dysfunction, developed in relation to myocardial dysfunction and remodeling, is documented in 15%-25% of the population. However, its role in functional recovery and recurrent vascular events after acute ischemic stroke has not been thoroughly investigated.
Methods
In this retrospective observational study, we identified 2,827 ischemic stroke cases with adequate echocardiographic evaluations to assess LV diastolic dysfunction within 1 month after the index stroke. The peak transmitral filling velocity/mean mitral annular velocity during early diastole (E/e’) was used to estimate LV diastolic dysfunction. We divided patients into 3 groups according to E/e’ as follows: <8, 8-15, and ≥15. Recurrent vascular events and functional recovery were prospectively collected at 3 months and 1 year.
Results
Among included patients, E/e’ was 10.6±6.4: E/e’ <8 in 993 (35%), 8-15 in 1,444 (51%), and ≥15 in 378 (13%) cases. Functional dependency or death (modified Rankin Scale score ≥2) and composite vascular events were documented in 1,298 (46%) and 187 (7%) patients, respectively, at 3 months. In multivariable analyses, ischemic stroke cases with E/e’ ≥15 had increased odds of functional dependence or death at 3 months (adjusted OR [95% CI]: 1.73 [1.27-2.35]) or 1 year (1.47 [1.06-2.06]) and vascular events within 1 year (1.65 [1.08-2.51]). Subgroups with normal ejection fraction or sinus rhythm exhibited a similar overall pattern and direction.
Conclusions
LV diastolic dysfunction was associated with poor functional outcomes and composite vascular events up to 1 year.
Keywords: Left ventricular diastolic dysfunction, Recurrent vascular event, Functional outcome, Acute ischemic stroke
Introduction
A dysfunction in the diastolic relaxation of the cardiac left ventricle (LV), even in cases without typical symptoms of heart failure, is documented in 15% to 25% of the population, and its prevalence increases with age [1-3]. Currently, LV diastolic dysfunction appears to be a result of myocardial dysfunction and remodeling driven by endothelial inflammation and oxidative stress [4]. The importance of LV diastolic dysfunction is clear because even after controlling for comorbidities, it has been associated with the development of heart failure, future cardiovascular events, and increased mortality, even in asymptomatic subjects [5-7].
For stroke physicians, LV diastolic dysfunction has important clinical implications. A major symptom of LV diastolic dysfunction is exercise intolerance [8]; however, stroke survivors might not have enough exercise capacity when they have LV diastolic dysfunction. Therefore, their exercise prescriptions must be modified. Additionally, the individual risk for recurrent stroke or vascular events may be altered by the presence of asymptomatic LV diastolic dysfunction. However, its clinical implication has only been studied in relation to a potential source of cryptogenic stroke [9], although LV diastolic dysfunction could be evaluated by a routine cardiac echocardiography, which is widely available [10,11].
In this context, we hypothesized that LV diastolic dysfunction would have deleterious effects on functional recovery and vascular events after ischemic stroke. Thus, we attempted to address this question by analyzing approximately 3,000 consecutive ischemic stroke cases with prospectively collected outcome information.
Methods
Of 4,808 stroke patients admitted to the Seoul National University Bundang Hospital within 7 days after symptom onset between August 2007 and June 2013, we selected ischemic stroke cases whose ischemic lesions were documented by relevant neuroimaging studies (N=3,858) and subjects who underwent echocardiographic evaluation within 1 month from the index stroke (N=3,030). We excluded cases with inadequate echocardiographic data to evaluate the LV diastolic function (N=203). The analysis dataset consisted of 2,827 acute ischemic stroke patients with echocardiography data. This is a retrospective study undertaken for the quality improvement of stroke management, using a prospectively collected cohort. All participants in this study gave their informed consent. In addition, the study protocol conforms to the ethical guidelines of the 1975 Declaration of Helsinki as reflected in a priori approval by the institution’s human research committee. Finally, this study was approved by the Institutional Review Board at the Seoul National University Bundang Hospital [IRB approval No. B-1501-284-102].
We collected baseline demographic data and clinical information for all study participants, including age, sex, premorbid functional status, history of previous stroke, mechanism of ischemic stroke, National Institute of Health Stroke Scale (NIHSS) score, acute reperfusion treatment, medication at discharge, and cardiovascular risk factors. Cardiovascular risk factors included hypertension (previous use of antihypertensive medication, systolic blood pressure >140 mmHg, or diastolic pressure >90 mmHg at discharge); diabetes mellitus (previous use of glucose-lowering medication or hemoglobin A1c ≥6.5%); dyslipidemia (previous use of lipid-lowering medication, fasting low density lipoprotein cholesterol >160 mg/dL, or fasting total cholesterol >240 mg/dL); habitual smoking (current or past regular smoking); and atrial fibrillation. We also obtained laboratory information, including random glucose at presentation, hemoglobin, total cholesterol, and initial systolic and diastolic blood pressures.
A well-trained and experienced nurse (M-H. Y) prospectively collected the functional outcome status (modified Rankin Scale [mRS] scores) and vascular events after the index stroke through telephone interviews with the patients or their immediate caregivers or at their routine clinic visit. Prospective outcomes were determined at 3 months and 1 year after the index stroke. The missing prospective outcomes were as follows: 15 mRS scores and 0 vascular events at 3 months, and 316 mRS scores and 275 vascular events at 1 year.
In our institution, acute ischemic stroke patients undergo an echocardiographic evaluation to identify potential embolic sources and the coexistence of ischemic heart disease as part of the clinical routine, if the patients or their caregivers do not refuse the examination due to any reasons such as personal economic issues and poor cooperation. Echocardiographic data were extracted in a retrospective manner through the review of medical records. Experienced technicians and board-certified cardiologists, who were not aware of the study purposes or the patient outcomes, performed and interpreted transthoracic echocardiographic evaluations in accordance with the published and relevant current guidelines [12]. In brief, LV dimensions, both at end-diastole and at systole, were measured at the standard parasternal short-axis view of the papillary muscle level or parasternal long-axis view. The dimensions of the aortic root, sinotubular junction, and ascending thoracic aorta diameter were measured at the standard parasternal long-axis view. Peak early transmitral filling velocities during the early diastolic (E), late diastole (A) and deceleration time (DT) were imaged in the apical 4-chamber view at the tip of the mitral leaflets. A Tissue Doppler image was applied to the apical 4-chamber view to determine the mean early (e’) and late (a’) velocities at septal mitral annuli. The maximal left atrial (LA) volume was indexed to the body surface area to measure the LA volume index.
The E/e’ ratio has been proposed as a surrogate for LA pressure and plays a prominent role for the assessment of diastolic function in the guidelines. Therefore, we used the E/e’ ratio as the primary grading system to estimate the LV diastolic functional status, classifying the E/e’ ratio as <8, 8-15, and ≥15 [13]. To validate the results further, we also adopted another grading system and separated the patients into 4 groups in accordance with the current recommendations. 13 Normal LV diastolic function was defined by the presence of an e’ ≥8 cm/s, E/A ratio 0.8-1.5, DT 160-200 ms, and LA volume index <34. Grade I diastolic dysfunction represented an e’ <8 cm/s, E/e’ <8, E/A ratio <0.8, and DT >200 ms. An E/A ratio 0.8-1.5, e’ <8 cm/s, E/e’ 8-15, and DT 160-200 ms were defined as grade II diastolic dysfunction (pseudo-normal pattern). The most severe form of LV diastolic dysfunction (grade III) occurs with an E/e’ ≥15, E/A ratio ≥2, and DT <160 ms. To classify the status of LV diastolic function in the cases with an E/A ratio 0.8-1.5 or DT 160-200 ms, which might be observed in both normal diastolic function and grade II diastolic dysfunction, other parameters such as e’, LA volume index, and E/e’ ratio were used to determine the grade of diastolic function. Because the peak A velocity is unmeasurable in atrial fibrillation patients, we did not apply the E/A ratio for the grading of LV diastolic dysfunction in these cases. However, e’, DT, and E/e’, which are not significantly influenced by atrial performance, were used as parameters to measure LV diastolic function. Normal LV diastolic function was defined by the presence of an e’ ≥8 cm/s and DT 160-200 ms. An E/e’ <8, e’<8 cm/s, and DT >200 ms were defined as grade I diastolic dysfunction. For grade II dysfunction, the criteria were DT 160-200 ms, e’ <8 cm/s, and E/e’ 8-15. The patients with grade III dysfunction had a DT <160 ms, e’ <8 cm/s, and E/e’ ≥15.
The categorical variables are presented as frequencies (percentages), and the continuous variables are presented as the means±standard deviations or medians [interquartile ranges], as appropriate. The baseline characteristics were compared using chi-squared tests for the categorical variables and t tests for the continuous variables. In the current analyses, functional dependency or death (a mRS score of 2-6), recurrent strokes, and composite vascular events, including recurrent stroke, myocardial infarction, and vascular death (any death directly attributed from vascular events), were designated as major outcome variables at 3 months and 1 year after the index stroke. We constructed multivariable binary logistic regression models that included the major outcome variables as dependent variables and adjusted for age, sex, recanalization treatment, initial stroke severity, mechanism of ischemic stroke, hypertension, diabetes, dyslipidemia, habitual smoking, atrial fibrillation, hemoglobin, glucose level at presentation, total cholesterol, and pre-morbid mRS score. We also analyzed the pre-specified ordinal logistic regression models that included the continuous scale of the mRS scores as dependent variables. Thus, this analysis strategy appears to be more sensitive to the minor influence of predictor variables than classical binary logistics [14]. Additionally, we performed additional multivariable binary logistic regression analyses in several subgroups as follows: those with preserved ejection fraction, those without atrial fibrillation, and those who underwent echocardiographic evaluation after symptom onset. The balance of the baseline characteristics among the groups might not be obtained, and age and initial stroke severity might influence functional outcomes. Therefore, we divided the total cases into 4 groups using the median values of age and initial NIHSS score. We performed a stratified analysis on the following subgroups: 1) age <69 and NIHSS score <3; 2) age ≥69 and NIHSS score <3; 3) age <69 and NIHSS score ≥3; and 4) age ≥69 and NIHSS score ≥3. Each outcome index was analyzed using the available cases. We excluded from the analyses the cases whose clinical outcome information was unobtainable. Significance levels were set at a 2-tailed P value of <0.05. Statistical analyses were performed using Stata 13 (StataCorp LP, College Station, TX, USA).
Results
Of the 2,827 included subjects, 1,724 (61%) cases were male, and the mean age was 67±13 years old. The NIHSS score at presentation was 3 [1-6], and recanalization treatment was performed in 383 (14%) cases. The prevalence of major vascular risk factors was 69% hypertension, 31% diabetes, 24% dyslipidemia, 44% habitual smoking, and 15% atrial fibrillation. Among the included subjects, 2,651 (94%) cases had echocardiography performed within 7 days from stroke onset. The mean time from stroke onset to echocardiography was 1.99±3.54 days. The mean E/e’ across all cases was 10.6±6.4; with an E/e’ <8 occurring in 993 (35%) cases, 8-15 occurring in 1,444 (51%) cases, and ≥15 occurring in 378 (13%) cases. The echocardiographic grading of the LV diastolic dysfunction classified the cases into grade I in 41% (1,161), grade II in 12% (332), and grade III in 6% (181) of the included population. Echocardiographic profiles of the included subjects are as follows: 61.8±7.7% for ejection fraction, 66.64±25.52 cm/s for E, 78.38±20.62 cm/s for A, 5.31±3.44 cm/s for e’, 9.48±2.38 cm/s for a’, 206.61±71.68 ms for DT, 38.80±19.97 mL/m2 for LA volume index, and 1.31±0.40 for mean pulmonary artery systolic pressure; the end systolic and diastolic dimensions of LV were 29.54±5.86 and 46.56±5.65 mm, respectively. A regional wall motion abnormality was observed in 225 (8%) cases. Among the 936 (33%) cases who underwent the transesophageal echocardiographic evaluation, there were 13 patients with thrombi and 44 patients with spontaneous echo contrast in their LA cavity or appendage (Supplemental Table 1). Functional dependency or death was documented in 1,298 (46%) cases at 3 months and 1,017 (41%) cases at 1 year. Recurrent stroke occurred in 171 (6%) cases at 3 months and 215 (8%) cases at 1 year. The composite vascular events, including recurrent stroke, myocardial infarction, and vascular death, were documented in 187 (7%) cases at 3 months and 250 (10%) cases at 1 year. Compared with the patients with an E/e’ <8, the patients with an E/e’ ≥15 were more likely to be female, old, and exhibit more prevalent vascular risk factors and prominent neurological deficits (Table 1). The prevalence of functional dependency or death showed significant differences according to the level of E/e’ at both 3 months and 1 year. However, there were statistical differences in the event outcomes only at 1 year after the index stroke (Table 2). Echocardiographic profiles also differed according to the E/e’ level. Ischemic stroke patients with a higher E/e’ ratio also exhibited prevalent vascular risk factors (Supplemental Table 2). The prevalence of clinical outcomes is demonstrated in Supplemental Table 3. The distribution of possible cardioembolic sources revealed by the transesophageal echocardiographic evaluation is summarized in Supplemental Table 1.
Table 1.
Baseline characteristics of study population via the E/e’ level
| Variables | Level of E/e’ |
P for difference | ||
|---|---|---|---|---|
| <8 [N=993, 35%] | 8-15 [N=1444, 51%] | ≥15 [N=378, 13%] | ||
| Demographic information | ||||
| Male | 685 (69%) | 875 (61%) | 159 (42%) | < 0.01 |
| Age | 64±14 | 67±12 | 73 ± 12 | < 0.01 |
| Vascular risk factors | ||||
| Stroke | 166 (17%) | 257 (18%) | 73 (19%) | 0.51 |
| Hypertension | 612 (62%) | 1,043 (72%) | 300 (79%) | < 0.01 |
| Diabetes | 255 (26%) | 472 (33%) | 154 (41%) | < 0.01 |
| Hyperlipidemia | 202 (20%) | 372 (26%) | 102 (27%) | < 0.01 |
| Atrial fibrillation | 88 (9%) | 229 (16%) | 114 (30%) | < 0.01 |
| Habitual smoking | 483 (49%) | 634 (44%) | 116 (31%) | < 0.01 |
| Coronary heart disease | 56 (7%) | 110 (8%) | 60 (16%) | < 0.01 |
| Congestive heart failure | 1 (0.1%) | 6 (0.4%) | 6 (1.6%) | < 0.01 |
| Mechanism of ischemic stroke | < 0.01 | |||
| Large artery atherosclerosis | 427 (43%) | 578 (40%) | 114 (30%) | |
| Small vessel occlusion | 198 (20%) | 273 (19%) | 55 (15%) | |
| Cardioembolism | 150 (15%) | 313 (22%) | 145 (38%) | |
| Other determined etiology | 43 (4%) | 43 (3%) | 5 (1%) | |
| Undetermined etiology | 175 (18%) | 237 (16%) | 59 (16%) | |
| Stroke information | ||||
| mRS score 0 before index stroke | 871 (88%) | 1,259 (87%) | 319 (84%) | 0.25 |
| NIHSS at initial presentation | 3 [1-6] | 3 [1-6] | 4 [2-9] | < 0.01 |
| Initial systolic blood pressure (mmHg) | 154±26 | 155±27 | 155±28 | 0.92 |
| Initial random glucose (mg/dL) | 141±67 | 144±64 | 151±68 | 0.02 |
| Hemoglobin (g/dL) | 14±2 | 14±2 | 13±2 | < 0.01 |
| HbA1c (%) | 6.3 ± 1.3 | 6.4±1.3 | 6.5 ± 1.4 | < 0.01 |
| Total cholesterol (mg/dL) | 184±44 | 179±42 | 173±41 | < 0.01 |
| Hyperacute recanalization treatment | 121 (12%) | 188 (13%) | 72 (19%) | < 0.01 |
| Echocardiographic profile | ||||
| Ejection fraction (%) | 62.6±6.5 | 62.2±7.2 | 59.0±10.7 | < 0.01 |
| Preserved ejection fraction (>40%) | 977 (99%) | 1,416 (98%) | 350 (94%) | < 0.01 |
| E (cm/s) | 56.6±15.2 | 67.6±18.5 | 89.4±46.4 | < 0.01 |
| A (cm/s) | 72.4±17.5 | 80.1 ±18.2 | 89.5±3.11 | < 0.01 |
| e’ (cm/s) | 5.3 ± 4.7 | 5.6±2.5 | 4.1 ± 1.7 | < 0.01 |
| a' (cm/s) | 10.8±2.6 | 9.3 ± 2.0 | 7.7±2.0 | < 0.01 |
| Deceleration time (msec) | 203.9±61.3 | 203.7±70.4 | 225.2±95.5 | < 0.01 |
| Left atrial volume index (mm/m2) | 32.2±11.9 | 37.4±17.2 | 52.3±29.0 | < 0.01 |
| Left ventricular end systolic dimension (mm) | 29.2±5.5 | 29.9±6.1 | 29.0±5.8 | < 0.01 |
| Left ventricular end diastolic dimension (mm) | 46.6±5.5 | 46.7±5.7 | 46.0±5.8 | 0.11 |
| Mitral stenosis | 0 (0%) | 2 (0%) | 16 (4%) | < 0.01 |
| Mitral regurgitation | 455 (46%) | 759 (53%) | 242 (64%) | < 0.01 |
| Aortic stenosis | 11 (1%) | 24 (2%) | 15 (4%) | < 0.01 |
| Aortic regurgitation | 255 (26%) | 442 (31%) | 172 (46%) | < 0.01 |
| Hypertrophic cardiomyopathy | 6 (1%) | 15 (1%) | 14 (4%) | < 0.01 |
| Discharge medication | ||||
| Anti-diabetic agents | 161 (20%) | 346 (25%) | 112 (31%) | < 0.01 |
| Anti-hypertensive agents | 338 (41%) | 749 (54%) | 219 (60%) | < 0.01 |
| Anti-hyperlipidemic agents | 608 (74%) | 1,180 (85%) | 304 (84%) | < 0.01 |
| Anti-platelet agents | 851 (87%) | 1,180 (83%) | 276 (75%) | < 0.01 |
| Anticoagulant | 122 (12%) | 283 (20%) | 107 (29%) | < 0.01 |
mRS, modified Rankin Scale; NIHSS, National Institute of Health Stroke Scale; composite vascular events include recurrent stroke, myocardial infarction and vascular death after the index stroke; E, peak early transmitral filling velocities during early diastole; A, peak early transmitral filling velocities during late diastole; e’, mean early velocities at septal mitral annuli on Tissue Doppler image; a’, mean late velocities at septal mitral annuli on Tissue Doppler image.
Table 2.
Clinical outcomes according to the E/e’ level
| Variables | Level of E/e' |
P for difference | ||
|---|---|---|---|---|
| <8 [N=993, 35%] | 8-15 [N=1444, 51%] | ≥15 [N=378, 13%] | ||
| Outcomes at 3 months after stroke* | ||||
| mRS score 2-6 | 433 (43%) | 677 (45%) | 254 (63%) | <0.01 |
| Recurrent stroke | 51 (5%) | 99 (7%) | 30 (7%) | 0.13 |
| Composite vascular events | 60 (6%) | 104 (7%) | 34 (8%) | 0.21 |
| Outcomes at 1 year after stroke† | ||||
| mRS score 2-6 | 353 (38%) | 521 (40%) | 201 (58%) | < 0.01 |
| Recurrent stroke | 67 (7%) | 116 (9%) | 42 (12%) | 0.03 |
| Composite vascular events | 79 (8%) | 129 (10%) | 56 (16%) | < 0.01 |
mRS, modified Rankin Scale; composite vascular events include recurrent stroke, myocardial infarction and vascular death after the index stroke; E, peak early transmitral filling velocities during early diastole; e’, mean early velocities at septal mitral annuli on Tissue Doppler image.
Outcomes at 3 months after stroke were based on 2,812 cases for the mRS score and 2,827 cases for recurrent stroke and composite vascular events;
Outcomes at 1 year after stroke were based on 2,511 cases for the mRS score and 2,552 cases for recurrent stroke and composite vascular events.
The ischemic stroke cases with a baseline E/e’ ≥15 were significantly associated with functional dependence or death (mRS score ≥2) at 3 months (adjusted OR [95% CI]: 1.73 [1.27-2.35]) and 1 year (1.47 [1.06-2.06]) compared with the cases with an E/e’ -<8 (Figure 1). An E/e’ ≥15 also indicated increased odds of recurrent vascular events until 1 year after stroke (1.65 [1.08-2.51]); however, the associations with the 3-month event outcomes failed to reach statistical significance. Grade III in echocardiographic grading had similar associations with functional recovery, including poor functional outcomes at 3 months (1.68 [1.13-2.49]) and 1 year (2.01 [1.31-3.07]). However, echocardiographic grading was not associated with event outcomes (Supplemental Table 4).
Figure 1.
Multivariable logistic regression analyses between left ventricular diastolic dysfunction (E/e’) and functional recovery and event outcomes. Composite vascular events include recurrent stroke, myocardial infarction, and vascular death after the index stroke. OR, odds ratio; CI, confidence interval; mRS, modified Rankin Scale.
We performed several pre-specified sensitivity analyses to address the robustness and uncertainty of the main analyses (Table 3 and Supplemental Table 4). The ordinal logistic models consistently indicated that the putative LV diastolic dysfunction was associated with functional dependency after ischemic stroke. To address the precarious methodology in the measurement of diastolic dysfunction, we repeated the main analyses in the subgroups with a preserved ejection fraction or without atrial fibrillation. The overall pattern, direction, and strength of the association between diastolic dysfunction and outcomes after stroke were also comparable in the subsequent analyses.
Table 3.
Sensitivity analyses via the E/e’ level
| Analytic strategies | Marker of diastolic dysfunction |
|
|---|---|---|
| E/e' | OR [95% CI] | |
| Ordinal logistic regression models (continuous scale of mRS score as a dependent variable) | ||
| mRS score at 3 months | <8 | Reference |
| 8-15 | 1.00 [0.86-1.17] | |
| ≥15 | 1.58 [1.24-2.00] | |
| mRS score at 1 year | <8 | Reference |
| 8-15 | 1.00 [0.84-1.18] | |
| ≥15 | 1.58 [1.22-2.04] | |
| Subjects with preserved ejection fraction (N=2,751) | ||
| Functional dependency or death at 3 months (mRS score 2-6) | <8 | Reference |
| 8-15 | 0.98 [0.80-1.20] | |
| ≥15 | 1.69 [1.23-2.32] | |
| Composite vascular events at 3 months | <8 | Reference |
| 8-15 | 1.16 [0.82-1.65] | |
| ≥15 | 1.33 [0.80-2.21] | |
| Functional dependency or death at 1 year (mRS score 2-6) | <8 | Reference |
| 8-15 | 0.94 [0.75-1.17] | |
| ≥15 | 1.39 [0.99-1.97] | |
| Composite vascular events at 1 year | <8 | Reference |
| 8-15 | 1.16 [0.84-1.59] | |
| ≥15 | 1.68 [1.08-2.60] | |
| Subjects without atrial fibrillation (N=2,394) | ||
| Functional dependency or death at 3 months (mRS score 2-6) | <8 | Reference |
| 8-15 | 0.94 [0.76-1.17] | |
| ≥15 | 1.77 [1.26-2.50] | |
| Composite vascular events at 3 months | <8 | Reference |
| 8-15 | 1.16 [0.80-1.69] | |
| ≥15 | 1.36 [0.78-2.39] | |
| Functional dependency or death at 1 year (mRS score 2-6) | <8 | Reference |
| 8-15 | 0.89 [0.70-1.12] | |
| ≥15 | 1.37 [0.95-1.98] | |
| Composite vascular events at 1 year | <8 | Reference |
| 8-15 | 1.10 [0.79-1.54] | |
| ≥15 | 1.88 [1.17-3.00] | |
Multivariable models were adjusted for age, sex, hyperacute recanalization treatment, mechanism of ischemic stroke, hypertension, diabetes, hyperlipidemia, habitual smoking, atrial fibrillation, hemoglobin, initial random glucose, total cholesterol, NIHSS at initial presentation, and mRS score before the index stroke.
LV, left ventricle; OR, odds ratio; CI, confidence interval; mRS, modified Rankin Scale; composite vascular events include recurrent stroke, myocardial infarction and vascular death after the index stroke.
We further divided our subjects into 4 subgroups by their age (<69 and ≥69 years old) and neurological severity (NIHSS score <3 and ≥3). E/e’ 8-15 was not associated with poor clinical outcomes. We found that the overall direction of associations between E/e’ ≥15 and the clinical outcome indices were maintained throughout the subgroups, except for the group with age ≥69 and NIHSS score ≥3 at 3 months, although this finding lost statistical significance due to a decreased number of subjects (Supplemental Table 5).
Discussion
In our ischemic stroke population, more than half of the cases exhibited LV diastolic dysfunction, and approximately 10% of the patients exhibited profound dysfunction. LV diastolic dysfunction deteriorated the functional status of the patient over the course of stroke recovery and may have increased the risk of recurrent vascular events in ischemic stroke survivors.
Functional recovery at 3 months or 1 year after stroke was consistently hampered by the presence of LV diastolic dysfunction at baseline, both from the main dichotomous analyses and the additional shift analysis strategies. More than half of stroke survivors achieve functional independence 1 year after the index stroke [10]. However, stroke survivors face several obvious barriers, including physical disabilities, which function against their expected recovery [15]. Myocardial remodeling from endothelial inflammation and low nitric oxide bioavailability may cause decreased distensibility in the LV diastole period and interfere with the LV filling process with slow relaxation [16-18]. In clinical aspects, in addition to low intensity of exercise, early supervised aerobic training and more intensive mobilization also have been exercise goals for functional recovery after stroke [19]. Thus, LV diastolic dysfunction, even in asymptomatic cases, may impede exercise capacity [20], which is a vital requirement for functional recovery after stroke [21].
To prove the robustness of the documented association between LV diastolic dysfunction and outcomes after stroke, we performed several sensitivity analyses via the incorporation of an additional statistical model and cardiac subgroups. The overall pattern of the associations remained in the sensitivity analyses, such as a poor functional recovery from the advanced stages of LV diastolic dysfunction but increased event outcomes documented only in the extreme group of E/e’ values. LV diastolic dysfunction supposedly has a direct impact on recurrent events through impaired left atrial contractility and intracardiac stasis, both of which increase the possibility of thromboembolism [22].
Several points should be clarified regarding our study. First, among various indicators, we mainly used E/e’ to evaluate LV diastolic dysfunction, with the echocardiographic grading system as a supplementary tool, both of which had only marginal correlations (Supplemental Table 6). Because of the complex pathophysiology of diastole [23], a gold standard indicator for diastolic dysfunction has not been devised. A current review article supports uniform integrative multiparametric grading of diastolic function as recommended by the updated guidelines, but establishment of a uniform grading system is considered to be a challenge [13,23,24]. However, the key indices that are included for grading the diastolic function still yield discrepant information. Among the various echocardiographic markers representing diastolic function, E/e’ has been proposed as a surrogate for LA pressure and plays a prominent role in the guidelines [13]. In addition, E/e’ might be a feasible echocardiographic parameter for LV diastolic dysfunction even in the subjects with atrial fibrillation. Since the peak A velocity is unmeasurable in patients with atrial fibrillation, the value of the E/A ratio cannot be applied alone in these cases [13]. Other parameters are usually considered as supporting parameters of main parameters such as E/e’ and E/A. This result implies that a considerable amount of case mix exists in the LV diastolic dysfunction grading system and suggests that the development of more precise tools for investigating LV diastolic dysfunction is necessary. Until any tangible and intuitive parameter for ischemic stroke patients is devised, stroke physicians should be aware of this intricacy and maximally utilize the available echocardiographic parameters. Second, although all the echocardiographic findings were collected from all the patients who had been examined, 113 cases who underwent echocardiographic evaluation before stroke onset were excluded from the study, and resting 715 cases did not have echocardiographic evaluation at baseline. The retrospective design of this study might produce selection bias. Third, we do not have detailed information regarding the pharmacological or rehabilitation interventions after discharge, which may confound the association between LV diastolic dysfunction and stroke outcomes. Fourth, since we included the patients who underwent echocardiographic evaluation after the index stroke, there is the possibility of stroke-induced cardiac dysfunction such as myocytolysis or Takotsubo cardiomyopathy, which might be reversible. In addition, echocardiographic profiles at the acute stage of stroke might be different from late period due to various factors, e.g., fluid therapy, discontinuation of antihypertensive agents, and sympathetic activation. Although early diastolic LV wall or mitral annular velocity and LV filling flow propagation velocity might be relatively volume load-independent [25], a combination of other factors possibly influence the cardiac diastolic function. Thus, follow up echocardiography at a later stage would give more information on the association between LV diastolic dysfunction and clinical outcomes. Fifth, since the results of our study were derived from only an Asian population, validations in other ethnic groups might be necessary. Sixth, although initial stroke severity and age were included in multivariable models as covariates, the balance of baseline characteristics among the 3 groups might not be achieved. We performed additional stratified analyses by using the median values of age and initial NIHSS score (Supplemental Table 5). However, the results showed statistical insignificance or a wide range in the confidence interval, which might be influenced by low event rates of each outcome variable or other cardiac function status. Seventh, besides the history of atrial fibrillation that we included as a covariate in multivariable analyses, we need to consider possible effects of other cardiac function variables on the clinical outcomes.
Conclusions
From our study, we documented that LV diastolic dysfunction was associated with poor functional outcome and composite vascular events up to 1 year (independently of clinical variables including age and baseline NIHSS score). These findings suggest that echocardiographic evaluations for stroke cases, which are typically performed for etiologic work-ups, may provide potentially important prognostic factors for patients and mechanistic insights into functional recovery and recurrence after stroke. In addition, exercise prescriptions and rehabilitation therapy might need modification depending on whether LV diastolic dysfunction is present or not. Further studies in stroke victims that examine recent advances in pharmacological or exercise interventions to prevent functional deterioration or recurrent events are warranted [26,27].
Footnotes
This work was supported by Grant No. 02-2014-039 of the SNUBH Research Fund and a grant from the Korea Healthcare Technology R&DProject, Ministry of Health and Welfare, Republic of Korea (HI10C2020).
The authors have no financial conflicts of interest.
Supplementary Material
References
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