Abstract
Objectives
The severity of diastolic dysfunction is assessed using a combination of several indices of left atrial (LA) volume overload and LA pressure overload. We aimed to clarify which overload is more associated with the prognosis in patients with heart failure and preserved ejection fraction (HFpEF).
Setting
A prospective, multicenter observational registry of collaborating hospitals in Osaka, Japan.
Participants
We enrolled hospitalised patients with HFpEF showing sinus rhythm (men, 79; women, 113). Blood tests and transthoracic echocardiography were performed before discharge. The ratio of diastolic elastance (Ed) to arterial elastance (Ea) was used as a relative index of LA pressure overload.
Primary outcome measures
All-cause mortality and admission for heart failure were evaluated at >1 year after discharge.
Results
In the multivariable Cox regression analysis, Ed/Ea, but not LA volume index, was significantly associated with all-cause mortality or admission for heart failure (HR 2.034, 95% CI 1.059 to 3.907, p=0.032), independent of age, sex, and the serum N-terminal pro-brain natriuretic peptide (NT-proBNP) level. In patients with a higher NT-proBNP level, the effect of higher Ed/Ea on prognosis was prominent (p=0.015).
Conclusions
Ed/Ea, an index of LA pressure overload, was significantly associated with the prognosis in elderly patients with HFpEF showing sinus rhythm.
Trial registration number
UMIN000021831.
Keywords: adult cardiology, heart failure, clinical physiology, geriatric medicine
Strengths and limitations of this study.
The severity of diastolic dysfunction is assessed by a combination of several indices of left atrial (LA) volume and pressure overload.
The ratio of diastolic elastance (Ed) to arterial elastance (Ea), that is, Ed/Ea, is a novel index of LA pressure overload.
Although the indices of LA pressure and volume overload are high in patients with heart failure and preserved ejection fraction (HFpEF), it remains to be seen which LA overload is more associated with the prognosis in elderly patients with HFpEF.
The limitation of this study is its small sample size.
Introduction
Patients with heart failure and preserved ejection fraction (HFpEF) have an increased left atrial volume (LAV) and early transmitral flow velocity/the onset of early diastolic mitral annular velocity (E/é), as shown by non-invasive echocardiographic findings.1–3 E/é is positively correlated with left atrial (LA) pressure or pulmonary capillary wedge pressure.4–7 We previously reported that the LAV index (LAVI), a relative index of LAV overload, and the ratio of diastolic elastance (Ed) to arterial elastance (Ea) (Ed/Ea = (E/é)/(0.9×systolic blood pressure)), a relative index of LA pressure overload, are high in elderly patients with preserved ejection fraction with and without heart failure (HF).3 8 9 In the recommendations for left ventricular (LV) diastolic evaluation using echocardiography, the severity of diastolic dysfunction (DD) is assessed using a combination of several indices, such as early transmitral flow (E)/late transmitral flow (A), deceleration time, E/é, tricuspid regurgitation velocity and LAVI.7 10 Evaluation of disease severity based on these recommendations is useful for estimating the prognosis of patients with HFpEF.11 However, these non-invasive indices are related to either LA pressure overload or LAV overload, and which overload is more associated with the prognosis of these patients remains unclear. In this study, we aimed to identify a clinically significant echocardiographic index of LA pressure or volume overload for the prognosis of patients with HFpEF.
Methods
Study subjects
Of the 353 patients with prognostic data who were recruited from the Prospective Multicenter Observational Study of Patients with Heart Failure and Preserved Ejection Fraction (PURSUIT HFpEF) registry,3 12 129 patients were excluded because they showed atrial fibrillation before discharge and 32 patients were excluded because of poor echocardiographic data. Therefore, we enrolled 192 patients showing sinus rhythm (LV ejection fraction (LVEF) ≥50%; men/women, 79/113; mean age, 80 years) at discharge during the index hospitalisation with acute decompensated HF; patients were enrolled based on the Framingham criteria, and if they met the criteria of LVEF ≥50% on transthoracic echocardiography (TTE) and N-terminal pro-brain natriuretic peptide (NT-proBNP) ≥400 pg/mL on admission. We excluded patients with severe aortic stenosis, aortic regurgitation, mitral stenosis or mitral regurgitation due to structural changes in the valves detected by TTE on admission. The PURSUIT HFpEF registry is a prospective, multicenter observational registry in which collaborating hospitals in Osaka, Japan recorded clinical, echocardiographic and outcome data of patients with HFpEF. The registry was managed in accordance with the Declaration of Helsinki.
Echocardiography and laboratory testing
TTE was performed when the patients were in a stable condition before discharge. Echocardiographic measurements were obtained according to the American Society of Echocardiography or European Society of Echocardiography criteria during a stable sinus rhythm.10 13 Volumetry was standardised using the modified Simpson’s method, and the index was calculated as the LAV divided by the body surface area. As a marker of LA pressure overload for estimating LV diastolic function, we examined afterload-integrated Ed/Ea ((E/é)/(0.9×systolic blood pressure)).3 9 14 As relative markers of LAV overload, we also evaluated LAVI and LA ejection fraction calculated as stroke volume (SV)/LAV.15 The severity of LVDD was assessed according to the previous reports.10 11 In the first step, the following four parameters were used: E/é, é velocity, tricuspid regurgitation velocity and LAVI. In the second step, E/A, E wave, E/é, tricuspid regurgitation velocity and LAVI were used to determine DD grades 1–3.10 11 When DD was not observed in the first step, the patients were classified as DD grade 0. Laboratory data were examined when patients were stable before discharge.
Follow-up/clinical outcome
After discharge, all patients were followed up at the respective hospital. Survival data were obtained by dedicated coordinators and investigators through direct contact with patients or their physicians at the hospital, or in an outpatient setting, or via a telephone interview with their families or by mail. Data collection was performed using an electronic data capture system integrated into the electronic medical records developed at the Osaka University.16 In-hospital data were entered into the system and transferred to the data collection centre via a secure Internet connection for processing and analysis. The primary endpoints of this study were the composite of all-cause mortality and hospitalisation for worsening HF.
Patient and public involvement
No patient involved.
Statistical analysis
Continuous variables are expressed as mean±SD, whereas categorical variables are presented as frequencies and percentages. Differences in categorical variables between the groups were assessed using the χ2 test, and those in continuous variables were assessed using Student’s t-test or Welch’s t-test, as appropriate. Coefficients of correlations were assessed using the Pearson or Spearman model, and p values were examined using regression analysis. Survival curves were estimated using the Kaplan-Meier product-limit estimator, and the groups were compared using the log-rank test. The Cox HR was evaluated using univariable and multivariable analyses. In the multivariable analysis, age and sex, and NT-proBNP level, LAVI and Ed/Ea that were significantly associated with outcome in the univariable analysis were included. A p value of <0.05 was considered statistically significant. All statistical analyses were performed using EZR (Saitama Medical Centre, Jichi Medical University, Saitama, Japan), which is a graphical user interface for R (The R Foundation for Statistical Computing, Vienna, Austria).
Results
Clinical and laboratory characteristics of patients with HFpEF
During a median follow-up of 452 days, 50 patients had all-cause mortality or admission for worsening HF. There were significant differences between patients with and without all-cause mortality or admission for HF in terms of age (p=0.011), estimated glomerular filtration rate (eGFR) (p=0.026) and serum NT-proBNP (p=0.017) and albumin (p<0.001) levels (table 1). There were no significant differences in medications or the incidence of hypertension and dyslipidaemia, except for diabetes mellitus, between the two groups. With respect to echocardiographic parameters, LAVI (p=0.024), tricuspid regurgitation pressure gradient (TRPG, p<0.001) and Ed/Ea (p=0.019) but not SV/LAV, LV mass index (LVMI), LVEF, E/A, the deceleration time of the E wave, septal e′, lateral e′, or Ed = (E/e′)/SV at discharge, were significantly different between patients with and without all-cause mortality or admission for HF (table 2).
Table 1.
Patient characteristics before discharge
| All (n=192) |
All-cause mortality or | P value (– vs +) |
||
| Admission for heart failure | ||||
| – (n=142) | + (n=50) | |||
| Age, years | 80.0±10.0 | 78.9±10.1 | 83.1±9.1 | 0.011 |
| Male sex, n (%) | 79 (41) | 59 (42) | 20 (40) | 0.848 |
| Cardiothoracic ratio, % | 55.4±7.5 | 54.8±7.4 | 57.2±7.7 | 0.093 |
| Systolic blood pressure, mm Hg | 122±18 | 120±17 | 124±21 | 0.078 |
| Diastolic blood pressure, mm Hg | 64±12 | 65±12 | 62±11 | 0.212 |
| Heart rate, beats/min | 69±14 | 69±14 | 68±12 | 0.576 |
| Chronic obstructive pulmonary disease, n (%) | 11 (6) | 9 (7) | 2 (4) | 0.796 |
| Coronary artery disease, n (%) | 41 (21) | 31 (22) | 10 (20) | 0.785 |
| Diabetes mellitus, n (%) | 73 (38) | 48 (34) | 25 (50) | 0.043 |
| Dyslipidaemia, n (%) | 92 (48) | 65 (46) | 27 (54) | 0.316 |
| Hypertension, n (%) | 169 (88) | 121 (85) | 48 (96) | 0.077 |
| Laboratory data | ||||
| Haemoglobin, g/L | 1.10±0.18 | 1.11±0.18 | 1.05±0.19 | 0.062 |
| Albumin, g/dL | 3.3±0.5 | 3.4±0.5 | 3.1±0.6 | <0.001 |
| eGFR, mL/min/1.73 m2 | 42.3±22.1 | 44.4±21.7 | 36.3±22.6 | 0.026 |
| N-terminal pro-brain natriuretic peptide, pg/mL | 2971±8478 | 2096±4832 | 5557±14 490 | 0.017 |
| Medications | ||||
| Beta-blockers, n (%) | 109 (57) | 82 (58) | 27 (54) | 0.645 |
| Calcium-channel blockers, n (%) | 112 (58) | 80 (56) | 32 (64) | 0.344 |
| Diuretics, n (%) | 146 (76) | 105 (74) | 41 (82) | 0.251 |
| RAAS inhibitors, n (%) | 133 (69) | 94 (66) | 39 (78) | 0.119 |
| Statins, n (%) | 72 (38) | 50 (35) | 22 (44) | 0.269 |
Values are mean±SD or number (%).
eGFR, estimated glomerular filtration rate; RAAS, renin-angiotensin-aldosterone system.
Table 2.
Echocardiographic data before discharge
| All | All-cause mortality or | P value (– vs +) |
||
| Admission for heart failure | ||||
| – | + | |||
| LAD, mm | 41.2±7.6 | 40.4±7.9 | 43.3±6.5 | 0.021 |
| LAVI, mL/m2 | 50.5±25.7 | 47.9±23.2 | 57.6±30.8 | 0.024 |
| LVEDVI, mL/m2 | 56.1±20.3 | 55.9±21.2 | 56.8±17.6 | 0.786 |
| LVESVI, mL/m2 | 21.8±10.8 | 21.8±10.9 | 21.8±10.7 | 0.993 |
| SVI, mL/m2 | 34.3±12.0 | 34.0±12.7 | 35.0±10.0 | 0.652 |
| SV/LAV | 0.809±0.376 | 0.835±0.376 | 0.733±0.373 | 0.125 |
| LVEF, % | 61.4±6.8 | 61.3±6.7 | 62.0±6.8 | 0.502 |
| LVMI, g/m2 | 108.4±33.2 | 105.8±32.5 | 115.9±34.1 | 0.063 |
| TRPG, mm Hg | 27.2±9.3 | 25.8±8.5 | 30.9±10.4 | <0.001 |
| E/A | 1.00±0.57 | 1.00±0.61 | 1.01±0.47 | 0.897 |
| DcT of E wave | 0.22±0.06 | 0.22±0.06 | 0.22±0.07 | 0.468 |
| Septal e′ | 0.051±0.019 | 0.052±0.020 | 0.048±0.016 | 0.189 |
| Lateral e′ | 0.067±0.023 | 0.067±0.024 | 0.067±0.020 | 0.979 |
| Ed = (E/e′)/SV | 0.450±0.230 | 0.431±0.227 | 0.505±0.249 | 0.065 |
| Ed/Ea | 0.130±0.055 | 0.125±0.055 | 0.146±0.052 | 0.019 |
Values are mean±SD.
DcT, deceleration time; E, early transmitral flow velocity; e′, onset of early diastolic mitral annular velocity; Ea, arterial elastance; Ed, diastolic elastance; LAD, left atrial diameter; LAV, left atrial volume; LAVI, left atrial volume index; LVEDVI, left ventricular end-diastolic volume index; LVEF, left ventricular ejection fraction; LVESVI, left ventricular end-systolic volume index; SV, stroke volume; SVI, stroke volume index; TRPG, tricuspid regurgitation pressure gradient.
The correlations between Ed/Ea and LAVI (r=0.194, p=0.008) or SV/LAV (r = −0.180, p=0.017) were more significant than those between E/e′ and LAVI (r=0.155, p=0.034) or SV/LAV (r = −0.137, p=0.072). E/e′ (r=0.233, p=0.001) and Ed/Ea (r=0.222, p=0.002) showed a modest positive correlation with the NT-proBNP log-transformed level, although TRPG did not correlate with the NT-proBNP log-transformed level (r=0.147, p=0.060). LAVI and the NT-proBNP log-transformed level were significantly correlated (r=0.256, p<0.001).
Prognostic analysis
In the receiver operating characteristic (ROC) curve analysis for the prediction of all-cause mortality or admission for HF, the area under the curve of LAVI was slightly smaller than that of the NT-proBNP level and Ed/Ea (table 3). The Kaplan-Meier survival analysis clearly showed that LAVI>38 mL/m2 (p=0.016), Ed/Ea>0.121 (p=0.002) and NT-proBNP level >783 pg/mL (p<0.001) were significant for prognosis (figure 1). Although not shown, age >85 years (p<0.001), eGFR <39.8 mL/min/1.73 m2 (p=0.004) and TRPG >28 mm Hg (p<0.001) were also determinant factors. The albumin level was not a determinant factor (data not shown). The LVDD grade was also related to all-cause mortality or admission for HF in patients with HFpEF, as shown by the Kaplan-Meier survival curve analysis (figure 1) and Cox hazard analysis (HR 3.164, 95% CI 1.761 to 5.683, p<0.001). In the multivariable analysis of the Cox HR, Ed/Ea (p=0.032) was significantly associated with poor outcome, independent of age, sex, LAVI and serum NT-proBNP level (table 3).
Table 3.
Analytical data of prognostic factors for all-cause mortality or admission for heart failure in patients with heart failure and preserved ejection fraction
| ROC curve analysis | Cox hazard analysis | |||||||
| Univariable | Multivariable | |||||||
| Cut-off point | AUC | Ratio | 95% CI | P value | Ratio | 95% CI | P value | |
| Age | 85 | 0.628 | 2.855 | 1.634 to 4.99 | <0.001 | 1.736 | 0.934 to 3.225 | 0.081 |
| Sex | – | – | 0.965 | 0.547 to 1.701 | 0.903 | 1.223 | 0.638 to 2.345 | 0.544 |
| NT-proBNP | 783 | 0.695 | 3.432 | 1.652 to 7.133 | <0.001 | 3.152 | 1.422 to 6.987 | 0.004 |
| LAVI | 38 | 0.607 | 2.225 | 1.134 to 4.366 | 0.02 | 1.298 | 0.599 to 2.813 | 0.508 |
| Ed/Ea | 0.121 | 0.637 | 2.424 | 1.337 to 4.394 | 0.003 | 2.034 | 1.059 to 3.907 | 0.032 |
AUC, area under the curve; Ea, arterial elastance; Ed, diastolic elastance; LAVI, left atrial volume index; NT-proBNP, N-terminal pro-brain natriuretic peptide; ROC, receiver operating characteristic.
Figure 1.
The Kaplan-Meier survival curve analysis of patients with heart failure and preserved ejection fraction. LAVI >38 mL/m2, ratio of Ed/Ea >0.121, NT-proBNP level >783 pg/mL and left ventricular DD grade (0–1 vs 2–3) were significant factors for all-cause mortality or admission for heart failure. Criteria for left ventricular DD grade were adopted from the previous reports.10 11The Ed/Ea ratio was calculated as (E/e′)/(0.9×systolic blood pressure).3 8 DD, diastolic dysfunction; Ea, arterial elastance; Ed, diastolic elastance; LAVI, left atrial volume index; NT-proBNP, N-terminal pro-brain natriuretic peptide.
In the Kaplan-Meier survival curve analysis for all-cause mortality or admission for HF with a stratified examination using the NT-proBNP level and Ed/Ea, the patients with NT-proBNP level >783 pg/mL and Ed/Ea>0.121 exhibited the highest event rate (figure 2, log-rank test, p=0.015). The effect of higher Ed/Ea on all-cause mortality or admission for HF was obvious in patients with a higher NT-proBNP level.
Figure 2.
The Kaplan-Meier survival curve analysis for all-cause mortality or admission for heart failure with stratified examination using the ratio of Ed/Ea and NT-proBNP level in patients with heart failure and preserved ejection fraction. Patients with NT-proBNP level >783 pg/mL and Ed/Ea >0.121 exhibited higher all-cause mortality or admission for heart failure. In patients with a higher NT-proBNP level, the effect of a higher Ed/Ea on all-cause mortality or admission for heart failure was obvious. Ea, arterial elastance; Ed, diastolic elastance; NT-proBNP, N-terminal pro-brain natriuretic peptide.
Discussion
In this study, LA pressure overload, rather than LAV overload, was found to be a more useful marker of prognosis in patients with HFpEF. Our findings can help determine which single index of LA pressure overload is significantly associated with the prognosis. In particular, in patients with a higher NT-proBNP level, a higher Ed/Ea was associated with a poor prognosis.
The heterogeneity of the cardiac structure in patients with HFpEF is well known. Notably, there were no significant differences in the deceleration time of the E wave and E/A in patients with and without all-cause mortality or admission for HF. The LA structure and function most closely reflect haemodynamic stress and remodelling in HFpEF.17 The E/e′ ratio was reported to be a significant prognostic factor in the Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist (TOPCAT) trial18 and a systematic review.19 However, there are many important differences between our study and the TOPCAT trial: (1) the TOPCAT trial was an intervention study; (2) subjects in our study were 10 years older; (3) the inclusion criteria were different (ie, stable outpatients in the TOPCAT trial vs hospitalised patients with HFpEF in our study and patients with atrial fibrillation were included in the TOPCAT trial but excluded from our study) and (4) an essential factor for prognosis, such as serum NT-proBNP level, was included in the multivariable analysis of the Cox HR in our study.
As a single index of LA pressure overload among non-invasive echocardiographic findings, Ed/Ea may be more significantly associated with all-cause mortality or admission for HF. E/e′ is known to be the best-fit index for LA pressure among echocardiographic indices in HFpEF.17 Ed/Ea = (E/e′)/(0.9×systolic blood pressure) is the LA pressure relative to systemic pressure and may show the ratio of preload to afterload pressure of the left ventricle. Thus, the Ed/Ea ratio may be an index that reflects the whole left-sided heart function, including the atrioventricular-arterial interaction under a preserved LVEF. Furthermore, patients with a higher NT-proBNP level and higher Ed/Ea had the poorest prognosis. The NT-proBNP level is a powerful prognostic factor in HFpEF.20 Although NT-proBNP reflects cardiac morphology and function,21 it remains uncertain whether NT-proBNP levels solely reflect cardiac processes or whether it also plays a role independent of cardiac remodelling. Several recent studies have reported that NT-proBNP may be an additional marker of extracardiac vascular diseases.22 23 At least a part of the association of NT-proBNP with prognosis is independent of cardiac remodelling measures.24 In combination with the NT-proBNP level, the significance of higher Ed/Ea for evaluating the prognosis was obvious in elderly patients with HFpEF.
Among the indices of LAV overload, LAVI but not SV/LAV significantly differed between patients with and without all-cause mortality or admission for HF. As the area under the curve of LAVI in the ROC curve analysis was small and no significant finding was observed in the multivariable analysis of the Cox HR for all-cause mortality or admission for HF in patients with HFpEF, we conclude that an index of LA volume overload such as LAVI is not a suitable factor for evaluating prognosis. LAVI is an indicator of long-term elevation of LV filling pressure, and an enlarged LAVI may be a secondary phenomenon. Even in patients without all-cause mortality or admission for HF, the mean LAVI was 47.9 mL/m2, which was considerably higher than the criterion for LVDD (>34 mL/m2).
LV Ed is expressed as (E/e′)/SV25 or (E/e′)/LV end-diastolic volume.26 Ea was calculated as (0.9×systolic blood pressure)/SV.25 Although Ed and Ea were reported to be negatively correlated in younger patients with hypertension,27 both indices were higher in elderly women than in men under stable conditions.25 26 Elevated Ed in elderly women could be an epiphenomenon because of the associated increase in Ea. We previously reported that Ed/Ea is an index of the LV diastolic function relative to the afterload and can be calculated as (E/ev)/(0.9×systolic blood pressure) when Ed is (E/e′)/SV.8 9 Accordingly, Ed/Ea was not directly related to the parameters of cardiac volume, such as LAV and SV. We recently reported a larger LAV and higher Ed/Ea in elderly women with preserved ejection fraction, regardless of HF status.3 8 9 Ed/Ea is a novel afterload-integrated parameter for LV diastolic function that may be useful as a severity index for prognosis in elderly patients with HFpEF.
Limitations
Further studies are required to investigate differences in the clinical significance of Ed/Ea for prognosis between younger patients with normal renal function and moderate-to-severe LV hypertrophy and elderly patients (mean age, 80 years) with renal dysfunction (mean eGFR, 42.3 mL/min/1.73 m2) and mild LV hypertrophy (mean LVMI, 108.4 g/m2) included in our study. We could not discuss echocardiographic parameters in patients with atrial fibrillation. The role of the right side of the heart in prognosis, as possibly reflected in the involvement of TRPG, remains unclear in this study. Even in the small sample size, the multivariable Cox model with the number of variables included/input was within the rough rule of one variable per 10 events. Under this condition, Ed/Ea was a significant prognostic factor, independent of NT-proBNP level. Although our results need to be interpreted carefully, our finding that a higher Ed/Ea was associated with a poor prognosis in patients with a higher NT-proBNP level may be clinically important. We examined all-cause mortality rather than cardiac death because the determination of cardiac death can be challenging in elderly patients.
Conclusions
LA pressure overload, rather than LAV overload, is a useful marker of prognosis in elderly patients with HFpEF showing sinus rhythm. As an index for LA pressure overload among non-invasive echocardiographic findings, Ed/Ea provides additional prognostic information on the serum NT-proBNP level.
Supplementary Material
Acknowledgments
We thank Hiroyuki Kurakami and Tomomi Yamada for their statistical support. We also thank Nagisa Yoshioka, Kyoko Tatsumi, Satomi Kishimoto, Noriko Murakami and Sugako Mitsuoka for their excellent assistance with data collection.
Footnotes
Collaborators: Shunsuke Tamaki, Masatake Fukunami, and Takahisa Yamada, Osaka General Medical Center, Osaka, Japan; Takaharu Hayashi and Yoshiharu Higuchi, Osaka Police Hospital, Osaka, Japan; Masaharu Masuda, Mitsutoshi Asai, and Toshiaki Mano, Kansai Rosai Hospital, Amagasaki, Japan; Hisakazu Fuji, Kobe Ekisaikai Hospital, Kobe, Japan; Daisaku Masuda, Yoshihiro Takeda, Yoshiyuki Nagai, and Shizuya Yamashita, Rinku General Medical Center, Izumisano, Japan; Masami Sairyo, Yusuke Nakagawa, and Shuichi Nozaki, Kawanishi City Hospital, Kawanishi, Japan; Haruhiko Abe, Yasunori Ueda, Masaaki Uematsu, and Yukihiro Koretsune, National Hospital Organization Osaka National Hospital, Osaka, Japan; Kunihiko Nagai, Ikeda Municipal Hospital, Ikeda, Japan; Masamichi Yano, Masami Nishino, and Jun Tanouchi, Osaka Rosai Hospital, Sakai, Japan; Yoh Arita and Shinji Hasegawa, Japan Community Health Care Organization Osaka Hospital, Osaka, Japan; Takamaru Ishizu, Minoru Ichikawa, and Yuzuru Takano Higashiosaka City Medical Center, Higashiosaka, Japan; Eisai Rin, Kawachi General Hospital, Higashiosaka, Japan; Tetsuya Watanabe and Shiro Hoshida, Yao Municipal Hospital, Yao, Japan; Masahiro Izumi, Kinki Central Hospital, Itami, Japan; Hiroyoshi Yamamoto and Hiroyasu Kato, Japan Community Health Care Organization, Osaka Minato Central Hospital, Osaka, Japan; Kazuhiro Nakatani and Hisatoyo Hiraoka, Sumitomo Hospital, Osaka, Japan; Mayu Nishio and Keiji Hirooka, Saiseikai Senri Hospital, Suita, Japan; Takahiro Yoshimura and Yoshinori Yasuoka, National Hospital Organization Osaka Minami Medical Center, Kawachinagano, Japan; Akihiro Tani, Kano General Hospital, Osaka, Japan; Yasushi Okumoto and Hideharu Akagi, Kinan Hospital, Tanabe, Japan; Yasunaka Makino, Hyogo Prefectural Nishinomiya Hospital, Nishinomiya, Japan; Toshinari Ohnishi and Katsuomi Iwakura, Sakurabashi Watanabe Hospital, Osaka, Japan; Nagahiro Nishikawa and Yoshiyuki Kijima, Japan Community Health Care Organization, Hoshigaoka Medical Center, Hirakata, Japan; Takashi Kitao and Hideyuki Kanai, Minoh City Hospital, Minoh, Japan; Wataru Shioyama and Masashi Fujita, Osaka International Cancer Institute, Osaka, Japan; Koichiro Harada, Suita Municipal Hospital, Suita, Japan; Masahiro Kumada and Osamu Nakagawa, Toyonaka Municipal Hospital, Toyonaka, Japan; Ryo Araki and Takayuki Yamada, Otemae Hospital, Osaka, Japan; Akito Nakagawa and Yoshio Yasumura, Amagasaki Chuo Hospital, Amagasaki, Japan; Fusako Sera, Kei Nakamoto, Hidetaka Kioka, Tomohito Ohtani, Katsuki Okada, Hiroya Mizuno, Tomoharu Dohi, Takayuki Kojima, Hirota Kida, Akihiro Sunaga, Oeun Bolrathanak, Shinichiro Suna, Daisaku Nakatani, Shungo Hikoso, Toshihiro Takeda, Yasushi Matsumura, and Yasushi Sakata, Osaka University Graduate School of Medicine, Suita, Japan.
Contributors: (1) Conception and design of the study, acquisition of, and/or analysis and interpretation of data: SH, KT, YS, TM, YH, YN, HA and HF. (2) Discuss on the planning, drafting the article and/or revising it critically for important intellectual content: SH, TY, YY, SH, DN and YS. (3) Final approval of the version to be submitted: All authors.
Funding: This study was funded by Roche Diagnostics KK and FUJIFILM Toyama Chemical. No grant numbers were applicable.
Competing interests: None declared.
Patient and public involvement: Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
Provenance and peer review: Not commissioned; externally peer reviewed.
Contributor Information
Osaka Cardiovascular Conference Investigators:
Shunsuke Tamaki, Masatake Fukunami, Takaharu Hayashi, Masaharu Masuda, Mitsutoshi Asai, Toshiaki Mano, Daisaku Masuda, Yoshihiro Takeda, Yoshiyuki Nagai, Shizuya Yamashita, Masami Sairyo, Shuichi Nozaki, Yasunori Ueda, Masaaki Uematsu, Yukihiro Koretsune, Kunihiko Nagai, Masamichi Yano, Masami Nishino, Jun Tanouchi, Yoh Arita, Shinji Hasegawa, Takamaru Ishizu, Minoru Ichikawa, Yuzuru Takano, Eisai Rin, Tetsuya Watanabe, Masahiro Izumi, Hiroyoshi Yamamoto, Hiroyasu Kato, Kazuhiro Nakatani, Hisatoyo Hiraoka, Mayu Nishio, Keiji Hirooka, Takahiro Yoshimura, Yoshinori Yasuoka, Akihiro Tani, Yasushi Okumoto, Hideharu Akagi, Yasunaka Makino, Toshinari Ohnishi, Katsuomi Iwakura, Nagahiro Nishikawa, Yoshiyuki Kijima, Takashi Kitao, Hideyuki Kanai, Wataru Shioyama, Masashi Fujita, Koichiro Harada, Masahiro Kumada, Osamu Nakagawa, Ryo Araki, Takayuki Yamada, Akito Nakagawa, Fusako Sera, Kei Nakamoto, Hidetaka Kioka, Tomohito Ohtani, Katsuki Okada, Hiroya Mizuno, Tomoharu Dohi, Takayuki Kojima, Hirota Kida, Akihiro Sunaga, Oeun Bolrathanak, Shinichiro Suna, Toshihiro Takeda, and Yasushi Matsumura
Data availability statement
Data are available upon reasonable request. No additional data available.
Ethics statements
Patient consent for publication
Not applicable.
Ethics approval
This protocol (Osaka University Clinical Research Review Committee, R000024414) was approved by the ethics committee of Yao Municipal Hospital (2016-No.0006). All participants provided written informed consent.
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Data are available upon reasonable request. No additional data available.