Role of Calcium and Phosphate Ionic Product as an Early Marker of Vascular Calcification to Predict Cardiac Risk in Chronic Kidney Disease: A Case-control Study

M. Deepthi, M. Sirsikar, A. Shailaja, Shrabani Mohanthy
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Abstract

Introduction: Cardiovascular disease is the most leading cause of death in patients with Chronic Kidney Disease (CKD) and Vascular Calcification (CV) is one of the strongest predictors of cardiovascular risk. CV is a process characterised by thickening and loss of elasticity of muscular arteries walls which occurs in two distinct sites, the intimal associated with atherosclerotic plaques and medial calcification is characterised by vascular stiffening and arteriosclerosis with adverse clinical outcomes leading to cardiovascular mortality. Disturbed mineral metabolism such as increased serum phosphorus and ionic product may be one such risk factor and is emerging as a principle modifier of CV in the CKD subjects. Aim: To determine serum phosphorus and calcium in CKD patients and compare with calcium phosphorus ionic product as an early independent marker of CV in CKD to predict cardiac mortality. Materials and Methods: This was duration based case-control study conducted in Department of Nephrology, Vydehi Institute of Medical Sciences & Research Centre, Karnataka, India. Fifty cases of CKD presented in stage 3,4 and 5 and 50 healthy individuals between the age group 21-78 years were included as controls. Serum levels of Calcium, Phosphorous were analysed in autoanalyser, Ca x P ionic product was calculated, estimated Glomerular Filtration Rate (eGFR) was calculated by Modification of Diet in Renal Disease (MDRD) formula. All measured variables were compared with eGFR and compared between cases and controls. The results were presented as a mean±Standard Deviation (SD) and p-value <0.05 was considered as significant. Results: Mean age of cases were 47.74±11.01 years and 45.66±11.46 years were of controls. Clinically, confirmed CKD was found more in male patients 31 (62) compared to female 19 (38). eGFR (mL/min) cases (14.12±10.72) and (102.97±27.46) in control, Serum Creatinine (mg/dl) were 7.04±5.34 mg/dL in cases which was significantly more compared to control (0.84±0.20 mg/ dL). Serum Calcium (Ca) (mg/dL) 8.11±1.09 mg/dL in cases less compared with control 9.31±0.42 mg/dL, indicating hypocalcaemia. Serum Phosphrous (P) 5.2932±1.83 mg/dL) in CKD suggesting hyperphosphatemia compared to control (3.27±0.54 mg/dL). Calcium Phosphorus Ionic Product was 46.9108±14.77 in cases, elevated in CKD as compared to control (30.46±5.03). Statistically, significant result was found between serum phosphorus and calcium phosphorus ionic product (p<0.05), well compared with eGFR of stage 3, 4 and 5 CKD patients. Conclusion: Hyperphosphatemia and elevated calcium- phosphate ionic product is an early independent marker of calcification to predict cardiovascular risk in late stages of CKD.
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钙和磷酸盐离子产物作为血管钙化的早期标志物在预测慢性肾脏疾病心脏风险中的作用:一项病例对照研究
心血管疾病是慢性肾病(CKD)患者死亡的最主要原因,血管钙化(CV)是心血管风险的最强预测因子之一。心血管硬化是一个过程,其特征是肌肉动脉壁增厚和弹性丧失,发生在两个不同的部位,与动脉粥样硬化斑块和内侧钙化相关的内膜以血管硬化和动脉硬化为特征,具有不良的临床结果,导致心血管死亡。矿物质代谢紊乱,如血清磷和离子产物增加,可能是其中一个危险因素,并且正在成为CKD受试者CV的主要改变因素。目的:测定CKD患者的血清磷和钙,并与钙磷离子产物作为CKD CV的早期独立标志物进行比较,以预测心脏死亡率。材料和方法:这是在印度卡纳塔克邦Vydehi医学科学与研究中心肾内科进行的基于持续时间的病例对照研究。50例CKD表现为3,4和5期,50例年龄在21-78岁之间的健康个体作为对照组。用自动分析仪分析血清钙、磷水平,计算钙、磷离子产物,用肾脏疾病饮食修正(MDRD)公式计算肾小球滤过率(eGFR)。将所有测量的变量与eGFR进行比较,并在病例和对照组之间进行比较。结果以均数±标准差(SD)表示,p值<0.05为显著性。结果:患者平均年龄为47.74±11.01岁,对照组平均年龄为45.66±11.46岁。临床上,确诊CKD的男性患者31例(62例)多于女性19例(38例)。对照组eGFR (mL/min)为(14.12±10.72),对照组为(102.97±27.46),血清肌酐(mg/dl)为7.04±5.34 mg/dl,显著高于对照组(0.84±0.20 mg/dl)。血清钙(Ca) (mg/dL)(8.11±1.09 mg/dL)低于对照组(9.31±0.42 mg/dL),提示低钙血症。与对照组(3.27±0.54 mg/dL)相比,CKD患者血清磷(P)为5.2932±1.83 mg/dL,提示高磷血症。CKD患者钙磷离子积为46.9108±14.77,高于对照组(30.46±5.03)。血清磷、钙磷离子产物与3、4、5期CKD患者eGFR比较,差异均有统计学意义(p<0.05)。结论:高磷血症和磷酸钙离子产物升高是预测CKD晚期心血管风险的早期独立钙化指标。
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审稿时长
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