Background
The morbidity of secondary hyperparathyroidism is high in ESRD patients. Among all the complications, cardiovascular events are the leading causes of death, and the mortality caused by cardiovascular disease (CVD) is 10 to 100 times higher than that in the general population [
1]. While secondary hyperparathyroidism is an important risk factor of CVD in ESRD, PTX is an effective therapeutic method for severe SHPT unmitigated by medicine therapy. It has been reported that the cardiovascular mortality of patients who underwent successful PTX, registered 37–41% reduction [
2,
3]. However, the impact of PTX on left ventricular function remains obscure. Case report and small sample size studies have shown that the EF% and FS% of hemodialysis patients were significantly improved after the PTX [
4,
5]. This study was conducted retrospectively to fully explore the impact of PTX on the left ventricular function of dialysis patients.
Methods
Patients
The cohort of this retrospective study consisted of ESRD patients with SHPT received PTX from Oct 1, 2010, to Oct 1, 2016, at the First Affiliated Hospital, Zhejiang University School of Medicine. The inclusion criteria of PTX were according to Kidney Disease Improving Global Outcomes (KDIGO) 2009 guidelines [
6]. Accordingly, following patients were excluded: those having severe malnutrition, infection or inflammation; severe liver disease and coagulation disorders; complicated with a hematological disease or malignant tumors; having a history of acute cardiovascular and cerebrovascular events within 6 months; the parathyroid hormone (PTH)>100 ng/L within 1 month post- PTX; those who received the kidney transplantion during the follow-up; with follow-up < 1 year; received the PTX because of recurrence and data missing or insufficiency. Patients enrolled were followed for at least 1 year; baseline characteristics including age, sex, dialysis duration, dialysis modality, the primary diseases of ESRD, the number of parathyroid gland removed, the blood pressure pre- and 1-year post-PTX, the cardiovascular drugs used during the follow-up were collected. This study received approval from the Research and Ethics Committee of the First Affiliated Hospital, Zhejiang University School of Medicine.
Surgical methods and perioperative management
The surgery method employed was total PTX with forearm autotransplantation (tPTX+AT). The parathyroid tissues were forwarded for pathological examination intra- and post-operatively. Tiny pieces of parathyroid tissues were transplanted into patients’ forearms. Post-operatively, all patients were given substantial doses of intravenous calcium, oral calcium, and calcitriol supplement.
The biochemical parameters
We collected the biochemical parameters including pre-operative serum calcium, phosphate, alkaline phosphatase, parathyroid hormone, and albumin levels; monitored and observed them at 1 week, 1 month, 3 months and 1 year after the PTX.
The cardiovascular drugs and the blood pressure
We collected the cardiovascular drugs used during the follow-up, including angiotensin-converting enzyme inhibitors (ACEI), angiotensin-receptor blockers (ARBs), calcium blockers, cardiotonic β-blockers, isosorbide mononitrate and trimetazidine during the follow-up, and the blood pressure 1-year post-PTX.
The ultrasonic cardiogram
We also collected the ultrasonic cardiogram parameter pre- and 1- year post-PTX, including ejection fraction% (EF%), fractional shortening% (FS%), left ventricular end-diastolic diameter (LVDd), interventricular septum thickness (IVST), left ventricular posterior wall end-diastolic thickness (LVPWD), left atrial diameter (LA), aorta (AO), left ventricular end-systolic dimension (LVDs), left ventricular posterior wall end-systolic thickness (LVPWs), ventricular septal end-systolic thickness (IVSs).
We used the Devereux correction formula to calculate the Left ventricular mass index (LVMI).
Left ventricular mass (LVM, g) = 0.8 × 1.04{[LVDd (cm) + IVST (cm) + LVPWd (cm)]3-LVDd3} + 0.6;
Body surface area (BSA) (m2, female) = 0.0073 × height (cm) + 0.0127 × weight (kg) -0.2106;
BSA (m2, male) = 0.0057 × height (cm) + 0.0121 × weight (kg) + 0.0882;
LVMI (g/m2) = LVM/BSA.
The diagnostic criteria of left ventricular hypertrophy (LVH) are: LVMI≥95 g/m
2 (female), LVMI≥115 g/m
2 (male) [
7].
The improvement of LV systolic function was defined as the improvement of the EF% measured by echocardiography to an increase of 10% or greater in its absolute value 1-year post-PTX.
The primary and the secondary evaluation items
The primary evaluation items were: the change of ultrasonic cardiogram parameter pre- and 1-year post-PTX; the influence factor for the overturn of LVH; the influence factor for the improvement of EF%.
The secondary evaluation items included the biochemical parameters change pre- and post-PTX.
Data analysis
We used the Statistical Package for the Social Sciences (SPSS) version 23.0 (SPSS Inc., Chicago, IL, USA) for statistical analyses. We used Kolmogorov-Smirnov (KS) test to determine the normality of the continuous variables. Continuous variables were presented as mean ± SD or interquartile range, and categorical variables were presented as number and proportion. We used the paired t-test and Wilcoxon signed- rank sum test to check the difference between ultrasonic cardiogram parameters, LVM and LVMI, pre- and at one-year post-PTX. Moreover, We used the multiple logistic regression analysis to determine the influence factor for the overturn of LVH and the improvement of EF% one-year post-PTX. P < 0.05 was regarded as statistically significant.
Discussion
SHPT, a common complication of ESRD, is a clinical condition associated with bone and mineral disorder, anemia, pruritus, hypertension, vascular calcification,
cardiovascular disease, and sexual dysfunction [
8].
The morbidity and mortality of cardiovascular disease in dialysis patients is found significantly high, and the CVD accounts for about 50% of death in hemodialysis patients in European countries and the USA [
9‐
11]. Over the past decades, evidence has indicated that ESRD might induce myocardial ischemia and left ventricular dysfunction [
12]. Some findings have consistently shown that progressive LVH and cardiac fibrosis may cause diastolic and systolic dysfunction, but the pathophysiologic mechanism is still poorly understood [
13]. Several previous studies have documented that successful PTX is associated with reduced all-cause mortality and cardiovascular mortality [
3,
14,
15].
LVH and left ventricular diastolic dysfunction are the most common types of myocyte damage noticed in uremic patients. LVH is an adaptive response to pressure and volume overload. In dialysis patients, the incidence of LVH was reported about 68–89%, and it has been reported that LVMI increases substantially in the majority of dialysis patients who are treated with standard care, including angiotensin blockade, dialysis frequency, and anemia management [
16], and LVMI was associated with a higher CVD mortality [
1]. PTH is regarded as a uremic toxin as it could aggravate renal anemia and damage myocyte in hemodialysis patients. Previous studies have shown that the serum PTH level is independently associated with the LVH [
17], with the decline of PTH, the anemia alleviated, and the nutrition condition improved, and the toxicity of PTH receded. Recent experimental and clinical studies have highlighted the crucial role of fibroblast growth factor 23 (FGF23) receptor, Vitamin D deficiency, systolic blood pressure in induction and progression of LVH in CKD patients [
17‐
19]. A study showed the PTX could improve blood pressure by better control of BP, decrease afterload, and improve systolic function [
20].
Of all the patients, 43.75% diagnosed with LVH pre-PTX recovered from LVH after 1 year of PTX in our study, and we didn’t observe the significant influence factor for the overturn of LVH post-PTX including cardiovascular drugs and blood pressure in the multiple logistic regression analysis, so it can be confirmed the impact of PTX on the overturn of LVH further.
15% incidence of systolic dysfunction among newly started dialysis patients was reported, and there are case reports documenting an increase in EF% post-PTX [
4,
21]. Small sample research conducted by N. Goto indicated that ten patients’ EF% had markedly improved after 6 months of PTX [
5]. Traditional perspective studies confirmed that PTH is a promotion factor of LVH, while A. J. van Ballegooijen emphasized that the high concentration of PTH was significantly associated with low EF% [
22]. Lowering PTH levels can ameliorate the arterial calcification, decrease the afterload, and improve the EF% [
22].
In our study, we observed a generally rising trend in EF% and FS%, though there was no statistical difference observed in all patients. EF% was 66.69 ± 7.07% vs. 65.52 ± 7.80% and FS% was 37.01 ± 5.70% vs. 36.63 ± 5.80%. In the subgroup analysis of EF% ≤ 60% pre-PTX, we found that EF% and FS% after PTX significantly improved compared with pre-PTX and EF% level of 64.90 ± 7.90% vs. 55.71 ± 4.78%. And in these patients, 82.86% patients underwent an increase of 10% or greater in its EF% absolute value post 1 year of PTX, showing the markedly improvement of the LV systolic function. And in the multiple logistic regression analysis, we didn’t observe the significant relationship between the cardiovascular drugs, the blood pressure and the improvement of EF%, so we can affirm the effect of PTX on the improvement of the left ventricular systolic function. Compared with N Goto’s study, we conducted a longer and more comprehensive study.
By comparing our findings with previous ones, we conclude that the left ventricular function improved in ESRD patient after the PTX might be related to the causes, such as the decline of PTH after the PTX reduced or even overturned the damage of myocardium and ameliorated arterial calcification; the improvement of serum calcium and phosphorus abnormal also alleviated the vascular calcification; the improvement of nutrition status after the PTX was conducive to the recovery of the myocardium; PTX could improve blood pressure, with the better control of blood volume, the afterload declined, but in our study, the effect of BP didn’t observe in multiple logistic regression analysis.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.