Aortic stenosis is a risk factor for all-cause mortality in patients on dialysis: a multicenter prospective cohort analysis
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Aortic stenosis (AS) is common in patients on dialysis as well as in the general population. AS leads to difficulty with dialysis therapy because of unstable conditions such as intradialytic hypotension due to low cardiac output. However, the precise morbidity rates and risk factors of AS in patients on dialysis are unknown. Moreover, there are no large-scale observational studies regarding the association between AS in patients on dialysis and mortality. Therefore, we will investigate whether morbidity of AS in patients on dialysis is associated with mortality.
This is a multicenter prospective cohort analysis in the Tokai region of Japan. The 75 participating centers in this study will enroll approximately 2400 patients during 12 months, with or without AS. We started enrollment in July 2017 and will follow patents until June 2023. Transthoracic echocardiography will be performed to evaluate aortic valve. Parameters used for evaluation of aortic valve are mean pressure gradient between left ventricle and ascending aorta, aortic valve area, and maximum aortic jet velocity. We will diagnose AS using the criteria based on the 2014 American Heart Association/ American College of Cardiology Guideline. We will also perform transthoracic echocardiography at 12, 24, 36, 48, and 60 months. Survival prognosis and CV events will be determined at the end of June 2019, 2020, 2021, 2022, and 2023. Development of AS will be also evaluated as new onset or annual change in AS parameters. We will classify patients based on the presence or absence of AS and the stages of AS and will compare outcomes. Study outcomes will include the following: 1) all-cause mortality rates; 2) incidence of cardiovascular (CV) events; 3) CV-related mortality rates; 4) infection-related mortality rates; 5) new onset or development of AS.
We will consider the following hypotheses in this study, among others: The prevalence of AS is higher in dialysis patients; new onset and development of AS are associated with factors that are specific for dialysis, such as hyperphosphatemia, hyperparathyroidism, and medication; and outcomes in AS patients are poorer than in patients without AS at baseline.
UMIN000026756, Registered March 29 2017.
KeywordsAortic stenosis Dialysis Mortality CKD-MBD
American Heart Association/American College of Cardiology
Aortic valve area
Chronic kidney disease
Chronic kidney disease-mineral and bone disorder
Mean pressure gradient
Transcatheter aortic valve replacement
- V max
Maximum aortic jet velocity
The number of patients on maintenance dialysis is increasing worldwide. Diabetic nephropathy and hypertensive kidney disease account for most of these patients. Chronic kidney disease (CKD) is an independent risk factor for cardiovascular disease (CVD) [1, 2, 3, 4, 5]. Moreover, CVD, which leads to difficulty with dialysis therapy, is strongly associated with higher mortality. Coronary heart disease is a typical condition among CVDs. However, aortic stenosis (AS) is increasingly frequent in patients on dialysis. Previous reports have indicated that onset and progression of AS were related to aging, hypertension, diabetes, or lipid disorders [6, 7, 8]. Some epidemiological studies in the general population have shown that the morbidity rate of AS in those over 75 years old is 2–4% . Another general population study involving over 1.2 million individuals in Canada revealed that there were 20,995 patients who needed admission to hospitals or interventions for AS during 13 years of median follow-up . On the other hand, patients on dialysis are more likely to develop AS because of hyperphosphatemia, anemia, and other factors. However, accurate morbidity rates and risk factors of AS in patients on dialysis remain unknown. Moreover, there are no large-scale observational studies of the association between AS in patients on dialysis and mortality or onset of cardiovascular (CV) events. Hence, we will examine whether morbidity of AS in patients on dialysis is associated with mortality, using the database of the Tokai Aortic Stenosis Cohort in Patients on Dialysis. We believe this is the first study to evaluate this association. We will consider the following hypotheses in this study: 1) The prevalence of AS is higher in dialysis patients than in the general population. 2) New onset and development of AS are associated with traditional risk factors including aging and comorbidity of diabetes. 3) New onset and development of AS are associated with factors that are specific for dialysis such as hyperphosphatemia, hypercalcemia, and hyperparathyroidism. 4) Outcomes in AS patients are poorer than in patients without AS at baseline. 5) Outcomes are poorer according to AS stages.
The study is a multicenter, prospective cohort analysis in the Tokai region of Japan (Tokai Aortic Stenosis Cohort in Patients on Dialysis). We started enrollment in July 2017. The 75 participating centers in this study will enroll approximately 2400 patients during 12 months. Whether or not AS is present, we will include outpatients who are on maintenance dialysis for at least 12 months, aged over 20 years old, who undergo echocardiography every year, and agree with participation in this study.
Patient characteristics and data at the time of enrollment (baseline)
Baseline is defined as the time at which echocardiography is performed for the first time from July 2017 to June 2018. We will review the following: 1) age, sex, dialysis vintage, and original kidney disease, blood pressure, and resting heart rate; 2) comorbidities including diabetes mellitus and malignancy; 3) medical history including hospitalization because of heart failure within one year, coronary heart disease, aortic disease, stroke, peripheral artery disease, malignancy, and history of parathyroidectomy; 4) medication including renin-angiotensin blockers, calcium channel blockers, β blockers, vitamin D receptor activators, calcimimetics, phosphate binders, and warfarin; 5) laboratory data including hemoglobin, platelet count, and serum albumin, alkaline phosphatase, uric acid, urea nitrogen, creatinine, adjusted calcium, phosphorus, magnesium, intact parathyroid hormone (PTH), ferritin, and C-reactive protein levels.
Transthoracic echocardiography will be performed by using commercially available ultrasound systems owned by each facility during enrollment and the follow-up period every year by an experienced technician. All parameters will be assessed with B mode or tissue Doppler imaging. The investigator will be blinded to clinical data. Findings will be confirmed by a cardiologist. The parameters used for evaluation of aortic valve are mean pressure gradient (mPG) between left ventricle and ascending aorta, aortic valve area (AVA), and maximum aortic jet velocity (aortic Vmax). Doppler echocardiographic measurements will include the peak and transaortic mPG using the simplified Bernoulli equation, and the AVA using the standard continuity equation or planimetry method in most participating facilities. Continuous wave Doppler will be used at multiple windows to obtain the maximal jet velocity over the aortic valve as well. In addition to the AS parameters, we will measure various parameters including left ventricular ejection fraction, left ventricular mass index, left atrial diameter, and E/E’. We will also examine aortic valve calcification.
Definition and classification of AS
We will diagnose AS using the following criteria based on the 2014 American Heart Association/ American College of Cardiology (AHA/ACC) Guideline for the Management of Patients with Valvular Heart Disease: 1) mPG > 20 mmHg, or 2) AVA < 1.0 cm2, or 3) aortic Vmax > 2.0 m/s . We will evaluate stages A to D of AS according to the AHA/ACC Guideline. We will compare patient profiles, laboratory data at baseline, and outcomes including all-cause mortality and CV events among patients 1) with or without AS, and 2) 4 groups by stages.
July 1, 2017 – June 30, 2018
September 30, 2017
Fixation of baseline data
Preparation of paper on baseline
July 1, 2018 – June 30, 2023
Transthoracic echocardiography examination every year
Surveillance of outcomes every year
December 31, 2023
Fixation of final data
January 1, 2024 –
Preparation of papers on outcomes
Presentation at relevant national and international conferences
Study outcomes will include the following: 1) all-cause mortality rates, 2) incidence of CV events, 3) CV-related mortality rates, 4) infection-related mortality rates, and 5) new onset or development of AS. CV events are defined as heart failure requiring hospitalization, acute coronary syndrome, coronary artery disease requiring percutaneous coronary intervention, coronary artery bypass grafting, or medication, and stroke or peripheral artery disease requiring hospitalization. CV-related death is defined as death due to heart failure, acute coronary syndrome, aortic disease, or stroke. Infection-related death includes sepsis associated with peripheral artery disease. Development of AS is evaluated as new onset of AS or annual change in mPG, AVA, and aortic Vmax.
Steering Committee: Daijo Inaguma, M.D. (Fujita Health University), Yukio Yuzawa, M.D. (Fujita Health University), Midori Hasegawa, M.D. (Fujita Health University), Hiroki Hayashi, M.D. (Fujita Health University), Masao Mizuno (Mizuno Clinic)
Data Center: Department of Nephrology, Fujita Health University
Independent Outcome Evaluation Committee: Shoichi Maruyama, M.D. (Nagoya University), Yasuhiko Ito, M.D. (Aichi Medical University)
Biostatistics Adviser: Kunihiro Nishimura, M.D. (National Cerebral and Cardiovascular Center).
We will use SPSS statistics version 24 and the Easy R program  for statistical processing. Patient characteristics and baseline data will be compared between those with or without AS and those classified by AS stages using an unpaired t-test, analysis of variance for continuous variables, and Fisher’s exact test for nominal variables. We will compare incidence of all-cause mortality, CV events, CV-related mortality, infection-related mortality, and new onset of AS by using the log-rank test for Kaplan-Meier curves. The factors that contribute to all-cause mortality, CV events, CV-related mortality, infection-related mortality, and new onset of AS will be examined using univariate regression analysis. We will conduct multivariate Cox proportional hazards analysis using models with adjustment for some variables including age, gender, and factors that will be extracted as significant variables by univariate analysis. We will also examine factors contributing to annual change rates of mPG, AVA, and aortic Vmax with multiple regression analysis by using models. Continuous variables will be expressed as the mean and standard deviation, or the median and interquartile range, and categorical variables will be presented as a percentage. P-values less than 5% will be considered statistically significant.
The necessary sample size will depend on the endpoint being evaluated, although there are numerous endpoints in this study with various magnitudes of incidence rates. In addition, this study will function in part as explanatory research. Therefore, we decided to set the sample size as consecutive cases undergoing echocardiography in a year among participating facilities. We anticipate enrollment of over 2400 cases.
We will show real-world data about the relationship between AS and prognosis in dialysis patients. We consider this the first large-scale, prospective observational study. We planned this study to determine whether the prevalence of AS increases and is associated with poor prognosis among dialysis patients.
Risk for onset and development of AS in dialysis patients
Traditional risk factors for AS are aging, hypertension, comorbidity of diabetes, and hyperlipidemia [6, 7, 8]. In addition, increase in extracellular fluid volume, anemia, and increase in cardiac output due to vascular access lead to increased flow velocity and turbulence across the aortic valve in dialysis patients . These can lead to fibrosis and aortic valve calcification. Stinebaugh et al. reported in that higher resting heart rates in dialysis patients create mechanical shear stress on the aortic valve . Moreover, it is likely that chronic kidney disease-mineral and bone disorder (CKD-MBD) influence onset and development of AS in dialysis patients. Therefore, this study will examine blood pressure and heart rates before and after dialysis sessions, as well as the amount of interdialytic weight gain and hemoglobin level.
Calcification of aortic valve
Ectopic vascular and heart valve calcification is a typical condition in CKD-MBD [15, 16]. Guerraty et al. demonstrated that decline of glomerular filtration rate was associated with aortic valve calcification after adjustment for classic risk factors . Hyperphosphatemia, hypercalcemia, hyperparathyroidism, and other factors induce vascular calcification, while matrix GLA protein, klotho, magnesium, and other factors inhibit progression of vascular calcification. The mechanism of aortic valve calcification is not as well-understood as that of vascular calcification, although the same mechanism is likely. In addition, there is a possibility that calcium-containing phosphate binders and excess of the active form of vitamin D induce aortic calcification, while calcium-free phosphate binders and calcimimetics inhibit progression of aortic calcification. Accordingly, we will examine laboratory data including serum phosphorus, calcium, and PTH levels. Moreover, we will regularly collect information about medication, including type and dosage of phosphate binders, activated vitamin D, and calcimimetics.
Diagnosis and evaluation of AS
Echocardiography is used to examine the degree of AS severity by measuring mPG, AVA, and aortic Vmax. In this study, we will perform echocardiography and evaluate AS once a year starting at baseline. Hence, we will examine annual changes in the parameters. Brener et al. have shown that annual change rates in the peak/mean PG and AVA in AS patients were 8.3 mmHg, 6.3 mmHg and 0.14 cm2, respectively . Perkovic et al. demonstrated that the annual change rates of AVA and mPG were larger in dialysis patients than in patients without CKD, i.e., − 0.19 vs. -0.07 cm2, and 4.9 vs. 2.5 mmHg .
All-cause mortality in dialysis patients with AS
Some studies have reported the prognosis of dialysis patients with AS. Miura et al. reported that 167 of 519 severe AS patients, with AVA less than 1.0 cm2, died at a median of 3.5 years . In their study, renal impairment and dialysis were proven to be risk factors for mortality. Raggi et al. showed in their prospective study that the hazard ratio for all-cause mortality was almost doubled in patients with calcification of both the mitral and aortic valves . A feature of our study will be the larger scale as well as the longer follow-up period than in previous reports.
Treatment strategy of AS patients
According to the selection of treatment including medication, surgical aortic valve replacement, and transcatheter aortic valve replacement (TAVR), comorbidity and general condition will be considered [22, 23, 24]. The Society of Thoracic Surgeons predicted risk of mortality score or the EuroSCORE is generally used to evaluate risk for selection of surgical treatment. TAVR is likely to be performed in patients with high risk, including those on dialysis. However, the incidence of complications and mortality associated with treatment have been higher in dialysis patients [25, 26]. Optimal treatment selection by stages of AS in dialysis patients remains unknown. Therefore, we expect that the results of our study will lead to a treatment strategy for dialysis patients with AS.
The present study has the following limitations. First, this is an observational analysis, and there will be some differences in the baseline characteristics and laboratory data among the groups. Second, there will be differences in the type of echocardiographic devices among participating facilities.
We acknowledge the support provided by the following investigators and members of the Tokai Aortic Stenosis Cohort Study Group, who participate in this study. Hirofumi Tamai (Anjo Kosei Hospital), Shuichi Tsutsui (Aoi Central Hospital), Takuya Ueda (Aoi Clinic Nishiokazaki), Yukio Narita (Aoi Hina Dialysis Clinic), Fumio Sofue (Aoi Miai Clinic), Yasuhiro Hirano (Aoyama General Hospital), Masahiro Motokawa (Asuka Clinic), Masamiki Miwa (Atsuta Clinic), Nobuo Suzuki (Chiryu Clinic), Shinichiro Kojima (Chita Kojima Memorial Hospital), Hisato Takatsu (Chuno Kosei Hospital), Toshiyuki Akahori (Chutoen General Medical Center), Kazutaka Murakami (Gamagori Clinic), Yasunobu Shimano (Gojyogawa Rehabilitation Hospital), Takashi Miyazaki (Gokiso Jin Clinic), Kaori Baba (Hananoki Clinic), Yoshiyasu Iida (Hirabari Memorial Clinic), Haruki Endo (Itsuki Clinic Ishikawabashi), Ryuichi Furuya (Iwata city Hospital), Isao Aoyama (JCHO Chukyo Hospital), Yasuhide Mizutani (JCHO Yokkaichi Hazu Medical Center), Hachiro Seno (Josai Hospital), Takashi Nagaya (Juzen Clinic), Hirotake Kasuga (Kaikoukai Central Clinic), Satoshi Sugiyama (Kanayama Clinic), Kanako Kojima (Kenshinkai Kariya-Chuo Clinic), Kazuhiro Fujisawa (Kasugai Central Clinic), Tomohiko Naruse (Kasugai Municipal Hospital), Osamu Ishida (Kawana Hospital), Hideto Oishi (Komaki City Hospital), Akira Ono (Komaki Clinic), Hideaki Shimizu (Koujunkai Daido Hospital), Kiyonari Kato (Koujyukai Kasugai Hospital), Isao Ito (Koujyukai Rehabilitation Hospital), Shinji Yasutomi (Kuwana East Medical Center), Chikao Yamazaki (Masuko Clinic Subaru), Kaoru Yasuda (Masuko Memorial Hospital), Teppei Matsuoka (Medical Group Taiseikai), Yoshinari Tsuruta (Meiyo Clinic), Masao Mizuno (Mizuno Clinic), Masataka Ono (Mizuno Clinic Mizuhiro Bunin), Masahiro Okada (Moriyama Itsuki Hospital), Akiko Tanoue (Murase Hospital), Hirotake Kasuga (Nagoya Kyoritsu Hospital), Takaaki Obayashi (Narita Memorial Hospital), Itsuo Yokoyama (Narumi Clinic), Hiroko Kushimoto (Nishichita General Hospital), Hiroshi Hasegawa (Nishio Clinic), Masao Kawasumi (Nisshin Clinic), Atsushi Nomura (Nomura Naika), Yasuhiro Sakurauchi (Obu Clinic), Mitsuru Yamashita (Okehazama Clinic), Hiroaki Asada (Okazaki City Hospital), Keiji Ohara (Okazaki Mates Nephrology and Sleep Clinic), Sukenari Koyabu (Owase General Hospital), Masashi Tada (Saishukan Hospital Dialysis Treatment Center), Fumihiko Sato (Sato Hospital), Satoshi Yamaguchi (Seto Kyoritsu Clinic), Hiroshi Ogawa (Shinseikai Dai-Ichi Hospital), Yoshihiro Ota (Shinseikai Clinic), Yoshihiro Matsumoto (Shizuoka City Shizuoka Hospital), Satoki Otsuka (Sugiyama Hospital), Yasushi Namii (Tajimi Clinic), Yasushi Kasai (Takasu Hospital), Nobuo Kato (Togo Haruki Clinic), Makoto Nakayama (Tokai Chita Clinic), Haruo Sato (Tokai Clinic), Shinichiro Inaba (Tosei General Hospital), Masaya Shibata (Toyohashi Mates Clinic), Hiroshi Yamashita (TOYOTA Memorial Hospital), Junichiro Yamamoto (Tsushima City Hospital), MakotoYamaguchi (Yokkaichi Municipal Hospital).
This study is funded by Public Interest Incorporated Foundation Aichi Kidney Foundation. The selection committee of clinical trial department in prefecture of Aichi, Japan is consisted of 5 nephrologists (representative: Kenji Maeda, MD). The funding is provided for clinical research, which is available and in clinical setting, to about 20 researches a year.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
DI wrote this manuscript; DI and YS were involved in study design and protocol preparation; YY and MH lead study design and protocol preparation. YS and NS will collect and manage clinical data. DI and YS will analyze data. All authors reviewed this manuscript. All authors read and approved the final manuscript.
Ethics approval and consent to participate
This study will be conducted by following the Ethical guidelines for Clinical Research by the Japanese Ministry of Health, Labour, and Welfare (created July 30, 2003; full revision December 28, 2004; full revision July 31, 2008) and the Helsinki Declaration (revised 2013), and has been approved by the clinical research ethics committees at each participating facility (approval number: HM16–373). The subjects will receive oral and written explanations of the purpose of the study and provide consent. Trial registration is UMIN 000026756. Registered April 1, 2017.
Consent for publication
Not applicable. No individual details.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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