Clinical impact of echocardiography-defined pulmonary hypertension on the clinical outcome in patients with multiple myeloma.

Introduction

Multiple myeloma (MM) is caused by the malignant proliferation of plasma cells derived from monoclonal antibodies, and it can lead to multiple organ dysfunction, including that of the heart. The presence of several features, such as hypercalcemia, renal failure, anemia, and hemolytic bone lesions, distinguishes MM from other types of plasma cell proliferation. [ 1 ] According to the 2012 International Agency for Research on Cancer Data, MM has a worldwide age-standardized incidence rate (ASR) of 1.5/100,000, and the Asian countries have lower ASRs of MM than the Western countries. [ 2 ] However, there has been a two-fold increase in the incidence of MM in Asia over the last 10 years, which is striking considering that the 2012 Korean data on national cancer statistics indicated that the ASR of MM was 10 times higher than that recorded 20 years ago. [ 3 ] As the management of MM improves, the life expectancy at diagnosis has improved significantly. [ 4 ] However, only a small number of patients survive for more than 10 years. [ 5 ]

Pulmonary hypertension (PH), characterized by elevated pulmonary artery pressure and pulmonary vascular resistance, is a pathophysiological disorder that is a composite of the major cardiovascular and respiratory diseases. The World Health Organization (WHO) has classified PH into 5 groups according to the similarities in the pathophysiologic mechanisms and clinical presentation. [ 6 ] Although PH in MM has been rarely reported, the possible etiologies of PH in MM include left heart systolic disease, diastolic dysfunction (group 2), chronic thromboembolic PH resulting from thrombophilia (group 4), and adverse effects of various chemotherapy agents, in particular thalidomide/lenalidomide (group 1). PH has been reported as a complication of MM and other related monoclonal cell disorders in several cases. [ 7 – 10 ] The use of immunomodulating therapy is also an independent risk factor for PH. [ 11 , 12 ] However, only a few studies have reported on PH with respect to the incidence and prognosis of MM. The current study aimed to investigate the risk factors of transthoracic echocardiography (TTE)-defined PH and its impact on the clinical outcomes in patients with MM.

Material and methods

Study design and population

We enrolled 529 patients with MM who underwent TTE in Chonnam National University Hwasun Hospital between January 2007 and December 2017. Patients with pathologically proven involvement with amyloid light chain (AL) amyloidosis were excluded from the analysis. After excluding 139 patients who underwent TTE more than 1 month after the diagnosis of MM to minimize the cardiac effects of chemotherapy and other factors, a total of 390 patients were included and divided into 2 groups, namely, patients without PH and patients with PH, based on the TTE results. The study protocol was approved by the Chonnam National University Hospital Institutional Review Board (IRB number: 2015-05-092).

Study definitions

MM was diagnosed by bone marrow biopsy and confirmed by a hematologist. Based on the available literature, PH was defined by an estimated right ventricular systolic pressure (RVSP) > 40 mmHg on TTE. [ 13 ] We collected information on the baseline demographic characteristics, treatment history, laboratory findings, TTE characteristics, and clinical outcomes for all patients. We stratified the enrolled population according to several criteria, including the Revised International Staging System (based on the serum β2 microglobulin and albumin levels).

Hypertension was defined as a history of hypertension diagnosed and treated with medication, systolic blood pressure > 140 mmHg or diastolic blood pressure > 90 mmHg on at least 2 occasions, or current antihypertensive pharmacological therapy. Diabetes mellitus (DM) was defined as a history of DM, regardless of the duration of disease, need for antidiabetic agents, fasting blood glucose > 126 mg/dL, or HbA1c ≥ 6.5%. Congestive heart failure (CHF) was defined according to the New York Heart Association Classification III and IV symptoms.

To minimize interference of various treatments, we reviewed the treatment history of autologous peripheral blood stem cell transplantation and chemotherapy regimens. The primary outcome was all-cause death. The definition of cardiovascular death included acute decompensated heart failure (ADHF), myocardial infarction (MI), and sudden cardiac arrest. ADHF was diagnosed using the criteria of the current guidelines. [ 14 ] Briefly, a diagnosis of ADHF was based on clinical symptoms, such as dyspnea and fatigue, and signs, such as peripheral edema and pulmonary congestion using the Framingham criteria. If ADHF was caused by a condition other than coronary ischemia, the patient was considered not to have ADHF. The term “hopeless discharge” was used in cases where the patients with do-not-resuscitate consent were transferred to a hospice ward or ointment hospitals.

Echocardiographic examination

According to the current American Society of Echocardiography (ASE) guidelines, comprehensive echocardiography was used for analysis. Echocardiography images were obtained using two different commercially available echocardiography equipment systems (Vivid 7 and Vivid E9, GE Vingmed Ultrasound, Horten, Norway).

Chamber quantifications were performed according to the current ASE guidelines and included measurements of left ventricular (LV) end-diastolic and end-systolic dimensions (LVEDD and LVESD, respectively), left atrial diameter (LAD), and LV ejection fraction. [ 15 ] The early (E wave) and late (A wave) diastolic velocity of the mitral inflow were measured using the apical 4-chamber view during pulsed-wave Doppler, with the sample volume located at the tip of the mitral leaflets. The deceleration time of the E wave was measured as the time between the peak early diastolic velocity and the point at which the steepest deceleration slope was extrapolated to the zero line. The early diastolic (E’ wave) and late diastolic (A’ wave) of the septal mitral annulus were obtained using tissue Doppler imaging in the apical 4-chamber view. Diastolic dysfunction categorization was based on the E/A ratio. Grade 1 diastolic dysfunction was determined if the E/A ratio was < 0.8, and an E/A ratio of 0.8–1.5 was classified as grade 2 diastolic dysfunction, and E/A > 1.5 as grade 3. [ 16 ]

We measured the myocardial strain parameter of global longitudinal strain (GLS) using the standard methodology for speckle tracking. [ 17 ] After manual tracing of the LV endocardial border, the dedicated software automatically tracked the myocardium throughout the cardiac cycle in the apical 4-chamber, 2-chamber, and long-axis views. The GLS was obtained by averaging the peak values of segmental strain in the apical views. [ 18 ]

The peak tricuspid regurgitation velocity was measured using Doppler echocardiography to estimate the RVSP with the modified Bernoulli formula. Since the diameter of the inferior caval vein and its respiratory variation are poorly related to the right atrial pressure (RAP), we did not add the RAP to the RVSP to estimate the systolic pulmonary arterial pressure. [ 19 ]

Statistical analysis

All continuous variables are presented as means ± standard deviation, and discrete variables are expressed as counts and percentages. The differences between the groups were evaluated using the two-sample t test, χ 2 tests, or Fisher exact test, as appropriate. We prepared Kaplan-Meier curves for all-cause and cardiovascular death according to the PH and non-PH groups. Since the differences in the baseline characteristics could significantly affect the outcomes, sensitivity analyses were performed to adjust for confounding factors.

First, the following covariates were used in the multivariable Cox regression model: age ≥ 65 years, hypertension, DM, previous history of CHF, coronary artery disease, estimated glomerular filtration rate (eGFR) > 60 mL/min, immunoglobulin (Ig) A > 500 mg/dL, RVSP > 40 mmHg, LAD > 40 mm, E’ < 0.07 m/s, E/E’ > 14, and ejection fraction < 50%.

Second, Cox proportional hazard regression analysis was performed for the propensity score-matched cohort. The propensity score was estimated for the choice of PH using a multivariable logistic regression model that contained 22 covariates. The C-statistic of the logistic-regression model for propensity score matching was 0.702. The percent standardized mean differences after propensity score matching were within 10% across all matched covariates, indicating successful balance between the groups being compared.

All analyses were two-tailed, and a P value < .05 was considered to indicate significance. All statistical analyses were performed using the R Core Team (2015) (version 3.3.2, R Foundation for Statistical Computing, Vienna, Austria. URL https://www.R-project.org/ ).

Results

Baseline clinical characteristics, history of treatment, and laboratory findings

TTE-defined PH was observed in 107 patients (27%). The patients in the PH group were older (68.8 ± 7.8 vs 65.9 ± 9.6 years, P = .002) than those in the non-PH group (Table 1 ). There was no significant difference in the treatment, with the exception of cyclophosphamide administration, between the PH and non-PH groups. The laboratory findings indicated that the PH group had lower white blood cell counts (9.4 ± 6.3 vs 12.7 ± 23.8 103/L, P = .04) and eGFR (43.7 ± 27.6 vs 51.0 ± 31.1 mL/min/1.73 m 2 , P = .039) and a higher level of serum IgA (1,489.6 ± 2,472.0 vs 741.6 ± 1,585.6 mg/dL, P = .034) compared to the non-PH group (Table 2 ).

TTE characteristics

In terms of the TTE characteristics, the LVEDD, LVESD, and LAD were significantly greater in the PH group than in the non-PH group (Table 3 ). The LVEF was significantly lower and the E and A wave velocity, and E/E’ ratio were higher in the PH group than in the non-PH group. A higher prevalence of increasing severity diastolic dysfunction was observed in the PH group ( P = .023).

Clinical outcomes

During a median follow-up duration of 688 days (quartile 1 to 3: 209 to 1,316 days), all-cause death was noted for 134 patients (34.4%), and 38 patients (9.7%) died from cardiovascular causes (including ADHF, MI, and sudden cardiac arrest). All-cause and cardiovascular death rates were significantly higher in the PH group than in the non-PH group (47.7% vs 29.3%, P = .001; 25.2% vs 3.9%, P < .001, respectively), but neither non-cardiovascular death nor hopeless discharge rates were significantly different between the groups (22.4% vs 25.4%, P = 0.628; 22.4% vs 22.6%, P = 1.000, respectively; Fig. 1 ). In the Kaplan-Meier survival curve analysis, the PH group showed a significant association with increased all-cause and cardiovascular death rates compared to the non-PH group during clinical follow-up (Fig. 2 ).

Independent predictors of clinical outcomes

Table 4 showed that TTE-defined PH was a significant predictor of all-cause death [propensity score-adjusted hazard ratio [HR PS-adjusted ], 1.91; 95% confidence interval (CI), 1.24 to 2.95; P = .003], which was mainly attributable to an increased risk of cardiovascular death (HR PS-adjusted 6.18; 95% CI, 2.45 to 15.61; P = .001). Previous history of CHF and DM were also independent predictors of all-cause death, but a history of CHF was the only independent predictor of cardiac death.

Discussion

We investigated the impact of TTE-defined PH at diagnosis on the future clinical outcomes in patients with. The principal findings of the present study were as follows:

During the initial work-up for the patients with MM, TTE-defined PH was observed in 107 patients (27%) and older age, lower LVEF, a greater LAD, increased E/E’ ratio, and higher prevalence of increasing severity diastolic dysfunction was associated TTE-defined PH;

TTE-defined PH and a history of CHF were predictors of all-cause and cardiac death;

DM was an independent predictor of all-cause death in patients with MM.

TTE-defined PH in patients with MM

In the general population cohort, the prevalence of TTE-defined PH was approximately 2.6% to 9%. [ 20 , 21 ] In a previous single-center study, 32% (N = 39/123) of the patients with MM had TTE-defined PH. [ 22 ] In our study, 27% of the patients with MM had TTE-defined PH, and serum IgA levels were higher in the PH group than in the non-PH group (1,396.2 ± 2,470.3 vs 741.6 ± 1,585.6 mg/dL, P = .043). Mestecky et al showed that moderate relative serum viscosity is common in IgA myeloma, which is associated with high serum concentrations of IgA polymer. [ 23 ] The increase in the levels of procoagulant factors may also reflect an inflammatory reaction. A high incidence of acquired activated protein C resistance in patients with MM was observed, which disappeared during treatment and was associated with an increased risk of pulmonary embolism. [ 24 ] The proposed mechanisms include procoagulant antibody formation, increased blood viscosity, and interference with fibrin. [ 25 ] This result suggests that vasoactive mediators released by neoplastic cells, in addition to increased plasma viscosity, may play a role in the pathogenesis of PH in patients with MM.

TTE-defined PH and CHF

In the present analysis, TTE-defined PH (RVSP > 40 mmHg) and a history of CHF were the independent prognostic factors for all-cause and cardiovascular death in patients with MM. A previous study reported that the development and severity of PH in CHF were associated with increased mortality and morbidity, and RVSP was shown to be a strong predictor of mortality even after adjusting for diastolic dysfunction. [ 26 ] In our study, a history of CHF was an important prognostic factor, suggesting that additional precapillary components may have contributed to the development of PH. In addition, we found a greater LAD, increased E/E’ ratio, and higher prevalence of increasing severity diastolic dysfunction in the PH group. This is not simply attributable to an increase in the filling pressure on the left side and may also be partly due to active pre-capillary components, as revealed by an increased transpulmonary pressure gradient. Pathologically, pulmonary capillary remodeling, such as medial hypertrophy and muscularization, plays an important role in longstanding PH due to CHF. [ 27 ]

DM and MM

In our study, DM was an independent prognostic factor for all-cause death in the propensity-matched population. In a previous retrospective study, DM, steroid-induced DM in particular, was associated with poor clinical outcomes in MM. [ 28 ] MM cells express high levels of insulin receptor (IR) and insulin-like growth factor 1 receptor (IGF-1R), and insulin stimulates their growth through IR/IGF-1R hybrid receptor activation. [ 29 ] Activation of the IR/IGF-1R signaling pathway may result in dexamethasone resistance in myeloma cells. [ 30 ] Thus, the theory that endogenous and exogenous insulin and its analogs promote the growth of malignant cells and chemo-resistance seems to be an appropriate explanation for this finding in our study.

This is the first study to show that TTE-defined PH and CHF are an independent poor prognostic factor in multiple myeloma patients. Taken together, it is necessary to identify the underlying cause of PH because the treatment direction may differ accordingly. In the available literature, left heart disease is the most common cause of PH in the normal population [ 20 ] ; however, right heart catheterization is necessary for the differential diagnosis in patients with MM due to the presence of thrombophilia and hyperviscosity.

The main limitation of the present study is that the TTE findings cannot clearly identify the causal mechanisms of PH, which requires right heart catheterization and formal clinical evaluation. Second, it was a retrospective single-center observational study and included a relatively small number of patients. A large prospective cohort study is needed to determine whether each factor affects pulmonary hypertension. Third, we found no association of PH with pulmonary venous thromboembolism (4.6% vs 1.9%, /p = .340); however, this may be underestimated since patients with MM often have impaired renal function (eGFR, 51.0 ± 31.1 vs 43.7 ± 27.6 mL/min/1.73 m 2 ; P = .039) and are hesitant to receive enhanced CT (PH group n = 22 (20.6%) vs non-PH group n = 99 (35.0%), P = .009). Therefore, when PH in TTE is present, it is necessary to distinguish PTE through ventilation/perfusion lung scan that do not affect kidney function. Fourth, the duration of PH and follow-up for the degree of improvement were not investigated in the present study. Certainly, the presence of PH may influence the long-term mortality rates, but mortality associated with the improvement of PH is also likely to be important. No studies have shown the difference between improvement in PH and prognosis after treatment of multiple myeloma. So, further studies are needed. Fifth, the Doppler derivative pressure estimation may have been inaccurate in individual patients. Furthermore, since the transpulmonary pressure gradient may be highly underestimated and cannot be used to exclude PH, the pressure may also have been overestimated. [ 15 ] Finally, we adjusted for multiple confounding factors using the multivariable Cox regression model and propensity score matching; however, we cannot exclude the possibility of potential unknown confounding factors. Therefore, larger studies are needed to investigate the impact of PH in patients with MM.

Conclusions

This study demonstrates that the prevalence of TTE-defined PH is higher in patients with MM than in the general population. Moreover, TTE-defined PH and a history of CHF are the independent prognostic factors for all-cause and cardiovascular death in patients with MM. These results highlight the risk of associated cardiovascular disease in patients with MM and emphasize the importance of management strategies that prevent the deterioration of cardiac function.

Author contributions

Conceptualization: Hyun Ju Yoon, Kye Hun Kim.

Data curation: SungA Bae, Hyun Ju Yoon.

Formal analysis: SungA Bae, Hyun Ju Yoon.

Investigation: SungA Bae, Jae Yeong Cho, Hyung Yoon Kim, Min Chul Kim, Yongcheol Kim, Young Joon Hong, Hyung Wook Park, Ju Han Kim, Youngkeun Ahn.

Methodology: SungA Bae, Hyun Ju Yoon, Kye Hun Kim.

Project administration: Hyun Ju Yoon.

Supervision: Hyun Ju Yoon, Kye Hun Kim, Myung Ho Jeong.

Validation: Jeong Gwan Cho, Jong Chun Park.

Writing – original draft: SungA Bae.

Writing – review & editing: SungA Bae, Hyun Ju Yoon, Kye Hun Kim, Hyukjin Park.

Footnotes

Abbreviations: ADHF = decompensated heart failure, AL = light chain, ASE = American Society of Echocardiography, ASR = age-standardized incidence rate, CHF = congestive heart failure, DM = diabetes mellitus, DT = deceleration time of mitral inflow, eGFR = estimated glomerular filtration rate, GLS = global longitudinal strain, Ig = immunoglobulin, LVEDD = left ventricular end-diastolic diameter, LVESD = left ventricular end-systolic diameter, MI = myocardial infarction, MM = multiple myeloma, PAP = pulmonary arterial pressure, PH = pulmonary hypertension, PSM = propensity score-matched, RAP = right atrial pressure, RVSP = right ventricular systolic pressure, TRV = tricuspid regurgitation velocity, TTE = transthoracic echocardiography, WHO = World Health Organization.

How to cite this article: Bae S, Kim KH, Yoon HJ, Kim HY, Park H, Cho JY, Kim MC, Kim Y, Hong YJ, Park HW, Kim JH, Ahn Y, Jeong MH, Cho JG, Park JC. Clinical impact of echocardiography-defined pulmonary hypertension on the clinical outcome in patients with multiple myeloma. Medicine . 2020;99:43(e22952).

There was no additional financial support from public or private sources.

SB and KHK contributed equally to this work as the co-first authors.

The authors have no conflicts of interest to disclose.

Data sharing not applicable to this article as no datasets were generated or analyzed during the current study.

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