A Joint Evaluation of Neurohormone Vasopressin-Neurophysin II-Copeptin and Aortic Arch Calcification on Mortality Risks in Hemodialysis Patients

Objective: Systemic hypoperfusion is intricately involved in neurohormone secretion, vascular calcification (VC) related impaired vasodilation, and luminal stenosis. We aimed to conduct a joint evaluation of vasopressin-neurophysin II-copeptin peptide (VP) and advanced aortic arch calcification (AAC) on all-cause and cardiovascular (CV) mortality in maintenance hemodialysis (MHD) patients.

Methods: Unadjusted and adjusted hazard ratios (aHRs) of mortality risks were analyzed for different groups of VP and AAC in 167 MHD patients. The modification effect between higher VP and advanced AAC on mortality risk was examined using an interaction product term.

Results: Interactions between VP and AAC with respect to all-cause and CV mortality were statistically significant. In multivariable analysis, higher VP predicted all-cause and CV mortality [aHR: 2.2 (95% confidence interval (CI): 1.1–4.5)] and 2.6 (95% CI: 1.1–4.6), respectively. Advanced AAC was associated with incremental risks of all-cause and CV mortality [aHR: 2.1 (95% CI: 1.1–4.0)and 2.5 (95% CI: 1.0–4.3), respectively]. Patients with combined higher VP (>101.5 ng/mL) and advanced AAC were at the greatest risk of all-cause and CV mortality [aHR: 4.7 (95% CI: 1.2–16.2)and 4.9 (95% CI: 1.1–18.9), respectively].

Conclusion: Combined VP and advanced AAC predict not only all-cause but also CV death in MHD patients, and a joint evaluation is more comprehensive than single marker. In light of hypoperfusion and ischemic events in vital organs, VP and AAC could act as more robust dual marker for prognostic assessment.

Introduction

Patients undergoing maintenance hemodialysis (MHD) are at particular risk for early mortality, and cardiovascular (CV) deaths top the list as the leading cause (1). In light of this, searching for early warning signs with prompt intervention strategies to improve outcomes in MHD population is of prime importance. The hypothalamic-pituitary-adrenal (HPA) axis is stimulated in response to hemodynamic instability and systemic hypoperfusion in the emergency department and intensive care unit (2). Thus, vasopressin related neurohormones have emerged to assist clinicians with diagnosis and risk stratification in myriads of diseases, such as acute kidney injury, acute myocardial infarction (MI), heart failure, lower respiratory tract infection, stroke, and progression of chronic kidney disease (3–8). Furthermore, higher plasma concentrations of copeptin serve as novel biomarkers of combined CV events in MHD patients and significantly correlate with plasma concentrations of arginine vasopressin independent of critical illness (9, 10).

Physiologically, the primary determinant of the vasopressin system is a state of systemic hypoperfusion regardless of cardiac morphological determinants, including myocardial stretch, wall thickness or cavity dimensions (11–14). Nonetheless, MHD patients are especially prone to extraosseous vascular calcification (EOVC) associated luminal narrowing (15), leading to systemic hypoperfusion, reduced vascular compliance, impaired myocardial perfusion, elevated cardiac afterload, left ventricular hypertrophy, and ultimately sudden cardiac death (16–18). With regard to the extremely high prevalence of EOVC in MHD population, emerging evidence have highlighted that surrogate markers of EOVC can independently predict mortality risks (19, 20). Although EOVC can be immediately assessed by diverse diagnostic imaging tools, such as ultrasonography, computed tomography and angiography, chest radiograph has the advantages of being simple, inexpensive, and commonly applicable in daily clinical practice. Advanced aortic arch calcification (AAC) detectable on chest radiograph is identified as a robust predictor of CV mortality beyond traditional risk factors of atherosclerosis (21–24). Despite previous documented implications, the joint and interaction effects of higher plasma concentrations of vasopressin-neurophysin II-copeptin peptide (VP) and advanced AAC on mortality risks remained unclear. Thus, we aimed to conduct a joint evaluation of VP and AAC on all-cause and CV death risks in this population-based study of MHD patients.

Methods

Participants in the Cohort

The study had been approved by the Research Ethics Review Committee of En Chu Kong Hospital (ECKIRB1070102) in accordance with the ethical standards of the committee and the Helsinki declaration for research in humans. The written informed consent was obtained from the participants of this study. The relevant details of research methods were described previously (1, 25). Patients undergoing MHD treatment for at least 3 months were eligible for inclusion. All patients had to be older than 18 years of age and be receiving thrice-weekly MHD, and 185 patients were included. Eighteen patients were excluded from the study because of inadequate dialysis, terminal illness, active infections, advanced cancer, active hepatitis, severe protein-energy wasting, incomplete data, or unwilling to participate. Previous CV diseases (CVD) were defined as diseases attributable to myocardial ischemia and infarction, heart failure, symptomatic or life-threatening arrhythmia, cerebrovascular diseases, pulmonary embolism, and peripheral artery diseases.

Assessment of Exposures

The plasma VP and AAC were assessed at baseline. Plasma concentrations of VP were measured by a commercial quantitative enzyme-linked immunosorbent (ELISA) assay [Human vasopressin-neurophysin 2-copeptin ELISA Kit (Catalog Number: OKEH00396), Aviva Systems Biology, San Diego, CA, USA] in accordance with the manufactures' instructions. The standard chest radiograph was taken in posterior-anterior view. A clinician specializing in thoracic radiology and blinded to patient's clinical data independently reviewed one pre-selected standard chest radiograph obtained from each hemodialysis patient within or as close to the prespecified study period as possible. To determine the severity of AAC detectable on chest radiograph, we used a simple classification system: grade 0 (no visible calcification), grade 1 (small spots of calcification or single thin calcification of the aortic knob), grade 2 (one or more areas of thick calcification, but ≤ 50% of the circular area of the aortic knob), and grade 3 (circular calcification with > 50% of circular area of the aortic knob) (21). All patients were then stratified by AAC grading into the following two groups for statistical analysis: non-advanced AAC, patients with AAC grade 0 or grade 1; advanced AoAC, patients with AAC grade 2 or grade 3.

Assessment of Covariates

The following bio-demographic and laboratory parameters of each patient were recorded at baseline: age, gender, hypertension, diabetes mellitus (DM), previous CVD, AAC grading, hemodialysis (HD) vintage, systolic blood pressure, diastolic blood pressure, pre-dialysis blood urea nitrogen, normalized protein catabolic rate, creatinine, potassium, calcium, phosphorus, alkaline phosphatase (ALP), alanine aminotransferase, albumin, uric acid, total cholesterol, triglyceride, hemoglobin, platelet, intact parathyroid hormone (iPTH), and VP. HD vintage was defined as the duration of time between the first day of HD treatment and the first day that the patient entered the cohort. Blood pressure was recorded in the horizontal recumbent position before a midweek dialysis session. Pre-dialysis blood samples were obtained from the existing vascular access for further analysis. We adjusted plasma calcium according to the following equation: adjusted calcium, measured calcium+ [(4.0—plasma albumin in g/dL) × 0.8]. All laboratory tests were performed by standard procedures with certified methods.

Ascertainment of Outcomes

CV mortality in study patients was defined as death attributable to myocardial ischemia and infarction, heart failure, fatal arrhythmia, cardiac arrest because of other causes, cerebrovascular diseases, pulmonary embolism, peripheral artery diseases, and sudden otherwise unexplained death. Non-CV mortality was defined as all other causes of death, i.e., infection, malignancies, gastrointestinal hemorrhage, accidents and miscellaneous. All-cause mortality included CV and non-CV death. Patients were censored at last follow-up, switched to another dialysis unit or received a kidney transplant.

Statistical Analysis

Continuous variables were presented as mean ± standard deviation, and categorical variables were expressed as number (%). The correlation coefficients between covariates of interest were calculated. The univariate Cox regression analysis was performed to investigate the independence of risk factors associated with all-cause and CV mortality. The included subjects for final analysis were further stratified into higher and lower concentration groups by median values of VP and AAC, respectively. If hazard ratios (HRs) for the variables in the univariate analysis were significant, we would select the covariates into the multivariable regression model. Unadjusted and multivariable adjusted hazard ratios (aHRs) of mortality risks were calculated for different categories of plasma VP and AAC in the Cox regression model, including VP, AAC, DM, CVD, age, albumin, and ALP. The modification effect between plasma VP and AAC on mortality risks was determined using an interaction product term. According to methods previously described, an interaction occurs when the impact of a risk factor on outcome is changed by the value of a third variable, sometimes referred to as effect modification (19, 26).

We evaluated if the effect of VP on mortality risks was modified by AAC through incorporating an interaction term in the multivariable model. The cumulative survival probability and proportional hazards were presented by graphical methods. A significant product term indicates that there is an interaction between VP and AAC on the probability of mortality risk. A p < 0.05 was considered statistically significant. We used PASW Statistics SPSS version 22.0 (IBM, NY, USA) to analyze all bio-clinical data of MHD patients.

Results

The final study sample included 167 MHD patients with complete medical records and follow-up. Baseline bio-clinical data of the whole study population with comparison between survivors and non-survivors are summarized in Table 1. The mean age was 63.3 ± 9.8 years; ~47% were male. Prevalence of DM, hypertension, CVD and advanced AAC were 43.7, 53.3, 47.9, and 48.5%, respectively. The mean duration of follow-up was 26.1 ± 5.9 months. The overall mortality rate was 24.0% during follow-up, corresponding to an annual mortality rate of 11.0%. The incidence of event rate is 110.1 cases per 1,000 person-years. Twenty-eight patients (70.0%) died from CV causes, and 12 (30.0%) non-CV deaths occurred. The bio-clinical parameters that differed significantly between survivors and non-survivors included age, advanced AAC, history of CVD, DM, plasma levels of VP, albumin, ALP, and iPTH. The baseline data of four combined VP and AAC groups were compared and provided in the Table 2. Age, advanced AAC, history of CVD, DM, plasma levels of VP, albumin, and ALP still significantly differed among four combined VP and AAC groups. The comparisons between CV and non-CV deaths are summarized in Table 3. Patients who died as a result of CV death were more frequent to have a history of hypertension, prior CVD, higher levels of VP, albumin and creatinine.

TABLE 1

Table 1. Bio-clinical data of the whole study population with comparison between survivors and non-survivors.

TABLE 2

Table 2. Comparisons of baseline bio-clinical data among four combined VP and AAC groups.

TABLE 3

Table 3. Comparison of demographic characteristics and relevant laboratory data between CV deaths and non-CV deaths.

Table 4 summarizes the bivariate correlation coefficients between prognostic factors (VP and AAC) and bio-clinical parameters of interest in MHD patients at baseline. VP was significantly correlated with AAC (r, 0.28; p < 0.01), age (r, 0.25; p < 0.01), albumin (r, −0.20; p < 0.01), ALP (r, 0.23; p < 0.01), and previous CVD (r, 0.17; p < 0.05), respectively. AAC was in turn significantly correlated with age (r, 0.78; p < 0.01), ALP (r, 0.26; p < 0.01), and albumin (r, −0.22; p < 0.01). In the univariate Cox regression analysis of prognostic factors, higher VP levels, advanced AAC, previous CVD, DM, age, albumin, and ALP were significantly associated with all-cause mortality. Furthermore, higher VP levels, advanced AAC, previous CVD, DM, age, and ALP were significantly associated with CV mortality. The multivariable Cox regression model demonstrated higher VP, advanced AAC, previous CVD, DM, age, and albumin were still significantly associated with all-cause and CV mortality [aHR: 1.02 (95% confidence interval (CI): 1.01–1.02), 2.29 (95% CI: 1.14–4.59), 1.78 (95% CI: 1.10–3.53), 2.19 (95% CI: 1.09–4.37), 1.08 (95% CI: 1.01–1.17), 0.41 (95% CI: 0.21–0.82), and 1.00 (95% CI: 1.00–1.00), respectively]. However, we merely found that higher VP, advanced AAC, and age predicted CV mortality after multivariable adjustment [aHR: 1.03 (95% CI: 1.01–1.04), 2.40 (95% CI: 1.05–5.45), and 1.13 (95% CI: 1.02–1.26), respectively] (Tables 5, 6).

TABLE 4

Table 4. The correlation analysis in VP, advanced AAC, and clinical parameters of interest.

TABLE 5

Table 5. Univariate and multivariable Cox regression analysis of prognostic factors for all-cause mortality.

TABLE 6

Table 6. Univariate and multivariable Cox regression analysis of prognostic factors for CV mortality.

A Joint Evaluation of VP and AAC on All-Cause and CV Mortality Risks

The interaction analysis between higher VP and advanced AAC was statistically significant for all-cause mortality and CV mortality (p < 0.05, respectively). Figure 1 illustrated cumulative survival curves of all-cause and CV mortality with respect to higher and lower categories of plasma VP after multivariable adjustment in the Cox regression model. Multivariable-adjusted results demonstrated higher VP concentrations were associated with incremental risks for all-cause and CV mortality [aHR: 2.2 (95% CI: 1.1–4.5) and 2.6 (95% CI: 1.1–4.6), respectively] in MHD patients.

FIGURE 1

Figure 1. Cumulative survival curves of mortality risks with respect to plasma concentrations of VP after adjusting for advanced AAC, previous CVD, DM, age, albumin, and ALP during follow-up. (A) Higher concentration of VP (>101.5 ng/mL) was associated with an incremental risk of all-cause mortality. (B) The association between higher concentration of VP and CV mortality remained robust after multivariable adjustment. AAC, aortic arch calcification; ALP, alkaline phosphatase; CVD, cardiovascular diseases; DM, diabetes mellitus; VP, vasopressin-neurophysin II-copeptin peptide.

Figure 2 illustrated cumulative survival curves of all-cause and CV mortality with respect to advanced and non-advanced AAC after multivariable adjustment in the Cox regression model. Multivariable-adjusted results demonstrated advanced AAC was associated with incremental risks for all-cause and CV mortality [aHR: 2.1 (95% CI: 1.1–4.0) and 2.5 (95% CI: 1.0–4.3), respectively] in MHD patients.

FIGURE 2

Figure 2. Cumulative survival curves of mortality risks with respect to advanced AAC after adjusting for higher VP levels, previous CVD, DM, age, albumin, and ALP during follow-up. (A) Advanced AAC was associated with an incremental risk of all-cause mortality. (B) The association between advanced AAC and CV mortality remained robust after multivariable adjustment. AAC, aortic arch calcification; ALP, alkaline phosphatase; CVD, cardiovascular diseases; DM, diabetes mellitus; VP, vasopressin-neurophysin II-copeptin peptide.

Figure 3 illustrated various mortality risks (aHR) compared to the reference group (VP < 101.5 ng/mL and non-advanced AAC) in the multivariable Cox regression model. Figure 3A illustrated mortality risks (aHR) for all-cause mortality in the non-advanced AAC and higher VP (>101.5 ng/mL) group, advanced AAC and lower VP (<101.5 ng/mL) group, advanced AAC and higher VP (>101.5 ng/mL) group were 1.4, 2.4, 4.7, respectively. Figure 3B illustrated mortality risks (aHR) for CV mortality in the non-advanced AAC and higher VP (>101.5 ng/mL) group, advanced AAC and lower VP (<101.5 ng/mL) group, advanced AAC and higher VP (>101.5 ng/mL) group were 1.4, 1.6, 4.9, respectively. Among four combined VP and AAC groups, patients with higher VP (>101.5 ng/mL) and advanced AAC had the greatest mortality risks for not only all-cause mortality but also CV mortality.

FIGURE 3

Figure 3. Cumulative survival curves of mortality risks with respect to four combined groups of VP and AAC after adjusting for higher VP levels, advanced AAC, previous CVD, DM, age, albumin, and ALP during follow-up. (A) The group with combined higher concentrations of VP (>101.5 ng/mL) and advanced AAC showed the highest risk for all-cause mortality as compared to the reference group (VP < 101.5 ng/mL and non-advanced AAC). (B) The group with combined higher concentrations of VP (>101.5 ng/mL) and advanced AAC showed the greatest CV mortality risk as compared to the reference group (VP < 101.5 ng/mL and non-advanced AAC). The interaction analysis between higher VP and advanced AAC remained statistically significant for all-cause mortality and CV mortality (p < 0.05, respectively). AAC, aortic arch calcification; ALP, alkaline phosphatase; CVD, cardiovascular diseases; DM, diabetes mellitus; VP, vasopressin-neurophysin II-copeptin peptide.

The data of receiver operating characteristics (ROC) curves were demonstrated in the Supplemental Figures 1–6. The ROC analysis for all-cause mortality showed that the area under curve (AUC) of higher VP was 0.725 (95% CI = 0.643–0.808, Supplemental Figure 1), and the AUC of advanced AAC was 0.745 (95% CI = 0.672–0.817, Supplemental Figure 2). Moreover, the combination of higher VP and advanced AAC yielded a higher AUC value at 0.769 (95% CI = 0.685–0.852, Supplemental Figure 3). On the other hand, the ROC analysis for CV mortality showed that the AUC of higher VP was 0.764 (95% CI = 0.694–0.834, Supplemental Figure 4), and the AUC of advanced AAC was 0.760 (95% CI = 0.691–0.830, Supplemental Figure 5). Furthermore, the combination of higher VP and advanced AAC yielded a higher AUC value at 0.801 (95% CI = 0.724–0.877, Supplemental Figure 6). In light of this, combined higher VP and advanced AAC as a predictor increases the sensitivity and specificity for all-cause and CV mortality.

Discussion

The demand for earlier diagnosis, more precise prognostic evaluation and faster therapeutic decision-making process in diverse diseases has contributed to the ongoing investigations of novel biomarkers. The hope is that novel biomarkers will enable multidisciplinary specialist to identify the right level of care in clinical practice. In this cohort study of MHD patients, we show a brand new idea that a joint evaluation of VP and AAC provides more comprehensive warning effects and stronger predictive values for EOVC associated fatal events. In more depth, higher plasma concentrations of VP and advanced AAC interact to increase not only all-cause but also CV mortality. Several important findings in this work deserve further discussion.

VP is the key neurohormone derived from the magnocellular neurons of the hypothalamus. To a smaller extent, it is synthesized by other tissues including the sympathetic ganglia, adrenal glands, and the testis (27). VP is stored and secreted by granules within the posterior lobe of the pituitary, primarily as a response to hyperosmolarity, tissue hypoperfusion and low circulating effective volume (Figure 4). The synthesis of VP involves precursor peptides that are cleaved by a four-enzyme cascade into three major components: vasopressin, neurophysin II and copeptin. Since all the three cleavage products are generated in equal ratios (28), we examined the neurohormal effects of full-length peptide “vasopressin-neurophysin II-copeptin” in the current study.

FIGURE 4

Figure 4. Schematic diagram illustrating possible synthesis and release mechanisms for vasopressin-neurophysin II-copeptin in hemodialysis patients with vascular calcification. AVP, arginine vasopressin; GKR, amino acid spacer; NP II, neurophysin II; R, monobasic cleavage site; SP, signal peptide.

Why is VP sufficiently specific as a biomarker of all-cause and CV mortality risk? The most powerful stimulus for VP secretion is the elevation in plasma osmolality, even 1% change is sufficient. VP is also released under diverse stressful stimuli involved in complex endocrine, autonomic, and behavioral responses. Adaptations to stress stimuli activate the HPA axis and the sympathetic nervous system, either acute or chronic (29, 30). In other words, circulating VP corresponds with human body's stress level. Even mild stress circumstance contributes to VP release. Because corticotropin releasing hormone and VP induce the generation of adrenocorticotropic hormone and cortisol in critical illness, the relationship between plasma osmolality and VP is lost. With the strong ability of vasoconstriction in peripheral vessels, VP is particularly produced in response to acute ischemic events, including hypovolemic shock and tissue hypoperfusion. Under critical conditions, plasma VP concentrations exceed the physiological range with exponential levels 100- or 1,000-fold times the normal range (28). Accordingly, VP acts as a versatile prognostic biomarker for various diseases, e.g., acute MI, heart failure, pulmonary diseases, acute dyspnea, sepsis, hemorrhagic shock, and ischemic stroke (5, 31, 32). Especially type 2 MI, known as secondary MI due to acute imbalance in oxygen supply and demand other than coronary artery occlusion, is more common in patients with renal failure (32). To the best of our knowledge, it is the first study to prove VP is intricately involved in EOVC related fatal ischemic events.

Why does VP interact with AAC to increase the risk of CV mortality? EOVC associated impaired vasodilation and luminal narrowing play pivotal roles in the pathophysiology of ischemic events and sudden cardiac death in MHD population (18), and AAC has been recognized as a potent indicator of EOVC (24). Zhang et al. conducted a meta-analysis to prove that AAC predicts CV and all-cause mortality in dialysis population (24). Since VP secretion is attributed to systemic hypoperfusion, a joint evaluation of VP and AAC is required for risk stratification. Given that both VP and AAC were intricately involved in EOVC related fatal events, we assumed that the mortality risk would be augmented among patients with higher levels of VP and AAC. In this study, the modification effect between AAC and VP on all-cause and CV mortality was examined using an interaction product term according to previous methods of moderation analysis (1, 19, 26, 33). As expected, the effects of VP on all-cause and CV mortality risks were modified by AAC in the multivariable model. Our data show that patients with higher plasma concentrations of VP (>101.5 ng/mL) and advanced AAC have the greatest risk of all-cause and CV death. Furthermore, the effects of higher VP on mortality are abated by non- advanced AAC, and vice versa. The interaction effect between VP and AAC on all-cause and CV mortality was statistically significant (p < 0.05 for the interaction term, respectively).

Our study has several limitations. First, our sample size was relatively small and our patients were only Asian patients, limiting the statistical power and generalization to other populations. Second, cross-sectional laboratory values might not reflect substantial intra-individual variability over time. Third, our blood samples were measured immediately due to the short half-life of vasopressin associated peptides, limiting the clinical practicality. Finally, prospective nonrandomized analysis is subject to residual confounders.

Conclusions

Since risk stratification enables clinicians to identify the right level of care, searching for the novel biomarker is of prime importance for MHD patients with EOVC. Combined VP and AAC predict not only all-cause but also CV death in MHD patients, and a joint evaluation is more comprehensive than a single marker. In light of hypoperfusion and ischemic events in vital organs, VP and AAC could act as more robust dual marker for prognostic assessment.

Data Availability Statement

The datasets generated for this study are available on request to the corresponding author.

Ethics Statement

The studies involving human participants were reviewed and approved by The Research Ethics Review Committee of En Chu Kong Hospital (ECKIRB1070102). The written informed consent was obtained from the participants of this study.

Author Contributions

Y-SC, J-FC, and T-MW were responsible for study concept and design, interpretation of data, writing of the manuscript, and drafting of the manuscript. J-CL and S-WC assisted with biochemical and digital analysis. T-HT and P-CC assisted with statistical analysis. L-LW, W-NL, and C-YH provided experimental supports of detection of biomarkers. W-CK and C-CW implemented the manuscript revision.

Funding

This research was funded by NTU-CC-108L891002; NTU-CC-109L891002; Renal Care Joint Foundation; and Ministry of Science and Technology (MOST 108-2636-E-002-016, 108-2221-E-002-127-, and MOST 108-2320-B-385-001-).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The reviewer K-FH declared a past co-authorship with one of the authors C-YH to the handling Editor.

Acknowledgments

We would like to thank An-Shu Clinic and Jia Hsiang Clinic for clinical assistance.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmed.2020.00102/full#supplementary-material

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