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Left ventricular hypertrophy: is hyperphosphatemia among dialysis patients a risk factor?
Steven G Achinger1, Juan Carlos Ayus
1Dialysis Service, Texas Diabetes Institute, Bextar County Hospital District, San Antonio, TX 78201, USA.
Insights
Daily hemodialysis significantly reduces left ventricular hypertrophy (LVH) in end-stage renal disease (ESRD) patients by improving serum phosphorus control. This suggests a reversible cardiotoxic effect of phosphorus on the heart.
Area of Science:
- Nephrology
- Cardiology
- Mineral Metabolism
Background:
- Cardiovascular disease (CVD) is highly prevalent in end-stage renal disease (ESRD) patients, causing the majority of deaths.
- Abnormal mineral metabolism, particularly elevated serum phosphorus, is a novel cardiovascular risk factor in dialysis patients.
- Conventional hemodialysis is linked to significant left ventricular hypertrophy (LVH), even with controlled blood pressure and anemia.
Purpose of the Study:
- To investigate the impact of daily hemodialysis on left ventricular mass index (LVMI) in ESRD patients.
- To determine the relationship between serum phosphorus control and LVMI reduction.
- To explore the potential cardiotoxic effects of elevated serum phosphorus.
Main Methods:
- A study comparing conventional hemodialysis with daily hemodialysis.
- Monitoring of serum phosphorus levels and LVMI over a 12-month period.
- Analysis of phosphorus removal efficiency with daily hemodialysis.
Main Results:
- Daily hemodialysis significantly reduced LVMI compared to conventional hemodialysis.
- Improved control of serum phosphorus correlated with a reduction in LVMI.
- Daily hemodialysis demonstrated significantly improved phosphorus removal.
Conclusions:
- Elevated serum phosphorus may have a reversible cardiotoxic effect contributing to LVH in ESRD patients.
- Daily hemodialysis is an effective strategy for managing hyperphosphatemia and reducing LVH.
- Controlling serum phosphorus is crucial for improving cardiovascular outcomes in dialysis patients.
Abstract:
Cardiovascular disease occurs in ESRD patients at rates that are far higher than is seen in the general population, and cardiovascular deaths account for the majority of deaths among dialysis patients. Abnormal mineral metabolism is a novel cardiovascular risk factor among dialysis patients. Recently published results demonstrated that even with good control of BP and anemia, conventional hemodialysis is associated with significant left ventricular hypertrophy (LVH); however, daily hemodialysis was associated with a significant reduction in LV mass index (LVMI). Furthermore, it was shown that control of serum phosphorus correlates with the reduction in LVMI. These data suggest a novel mechanism for the deleterious effect of elevated serum phosphorus on cardiovascular outcomes among hemodialysis patients: LVH. Other investigators have noted an association of hyperphosphatemia and LVH; however, this study was the first to demonstrate that improvement in serum phosphorus is associated with reduction in LVM. In addition, it is shown that daily hemodialysis is an effective modality in improving serum phosphorus through significantly improved phosphorus removal. Elevated serum phosphorus leads to vascular calcification, which can lead to LVH by decreasing vascular compliance. However, our study showed an improvement in LVMI during a 12-mo period. Because vascular calcification is unlikely to remit over this time period, it is proposed that serum phosphorus has a reversible, cardiotoxic effect that leads to LVH that can be reversed successfully with good control of serum phosphorus.
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