评估慢性肾病患者的全血细胞计数和肝酶

A. Shafique, H. Javaid, H. Bajwa, R. Anwar, M. Yaseen, .. Sana
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引用次数: 0

摘要

慢性肾功能衰竭(CRF)是全球健康面临的重大挑战,慢性肾脏病(CKD)的特征是肾脏受损或肾小球滤过率(GFR)持续低于 60 毫升/分钟超过三个月。这项观察性研究于 2023 年 1 月至 7 月在费萨拉巴德进行,旨在评估 CKD 不同阶段的血液学变量和肝酶。研究采用非概率目的性抽样,收集了 144 份慢性肾功能衰竭患者档案和 48 份健康对照组档案,其中不包括特殊情况。根据肾病饮食改良(MDRD)算法确定 CKD 分期,将患者分为轻度(A 组)、中度(B 组)、重度(C 组)CKD 和对照组(D 组)。数据分析使用 SPSS v23 进行。列出了四个组中每个参数的平均值(± SD)。与对照组相比,CKD 患者的血红蛋白水平(Hb g/dl)呈下降趋势,对照组为 13.7 ± 1.50,第 1 组为 11.7 ± 0.64,第 2 组为 9.7 ± 0.57,第 3 组为 6.7 ± 1.5。与对照组相比,慢性肾脏病患者的红细胞计数(RBCs per million/mm3)也逐渐下降,各组分别为 5.48 ± 0.59、4.62 ± 0.15、3.57 ± 0.28 和 2.81 ± 0.23。相反,白细胞计数(WBC 千/立方毫米)随着慢性肾功能衰竭的进展而增加,对照组为 8406 ± 1383,第 1 组为 10674 ± 1006,第 2 组为 12028 ± 643.5,第 3 组为 13564 ± 741.29。同样,与对照组相比,CKD 患者的血小板计数(lakh/ul)呈下降趋势,分别为 324708 ± 112970、235458 ± 63853、144979 ± 6935.8 和 126333 ± 4768.3。肝酶分析显示,随着慢性肾功能衰竭的进展,天冬氨酸氨基转移酶(AST)和丙氨酸氨基转移酶(ALT)水平逐渐下降。AST 水平(U/L)从对照组的 29.104 ± 3.130 降至第 3 组的 7.5825 ± 1.543,而 ALT 水平(U/L)从对照组的 48.145 ± 4.9679 降至第 3 组的 12.270 ± 3.3500。我们的研究结果表明,随着慢性肾脏病的发展,血红蛋白、红细胞计数、血小板计数和肝酶水平(谷草转氨酶和谷丙转氨酶)会下降,而白细胞计数会增加。这些对血液和肝脏生物标志物的深入研究强调了慢性肾功能衰竭病理的动态性质,并可为临床管理策略提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ASSESSMENT OF COMPLETE BLOOD COUNT AND LIVER ENZYMES IN CHRONIC KIDNEY DISEASE PATIENT
Chronic renal failure (CRF) poses a significant global health challenge, with chronic kidney disease (CKD) characterised by kidney damage or a glomerular filtration rate (GFR) persistently below 60 ml/min for over three months. This observational study, conducted in Faisalabad from January to July 2023, aimed to evaluate haematological variables and liver enzymes across different stages of CKD. Using non-probability purposive sampling, 144 CKD patient files and 48 healthy control files were collected, excluding specific conditions. CKD staging was determined using the Modification of Diet in Renal Disease (MDRD) algorithm, categorizing patients into mild (Group A), moderate (Group B), severe (Group C) CKD, and controls (Group D). Data analysis was performed using SPSS v23. Mean ± SD values were presented for each parameter across the four groups. Haemoglobin levels (Hb g/dl) exhibited a decreasing trend in CKD patients compared to the control group, with values of 13.7 ± 1.50 in controls, 11.7 ± 0.64 in Group 1, 9.7 ± 0.57 in Group 2, and 6.7 ± 1.5 in Group 3. Red blood cell count (RBCs per million/mm3) also decreased progressively in CKD patients compared to controls, with values of 5.48 ± 0.59, 4.62 ± 0.15, 3.57 ± 0.28, and 2.81 ± 0.23 in the respective groups. Conversely, white blood cell counts (WBC thousand/mm3) increased with CKD progression, showing values of 8406 ± 1383 in controls, 10674 ± 1006 in Group 1, 12028 ± 643.5 in Group 2, and 13564 ± 741.29 in Group 3. Similarly, platelet counts (lakh/ul) exhibited a decreasing trend in CKD patients compared to controls, with values of 324708 ± 112970, 235458 ± 63853, 144979 ± 6935.8, and 126333 ± 4768.3, respectively. Analysis of liver enzymes revealed a progressive decrease in aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels as CKD advanced. AST levels (U/L) decreased from 29.104 ± 3.130 in controls to 7.5825 ± 1.543 in Group 3, while ALT levels (U/L) decreased from 48.145 ± 4.9679 in controls to 12.270 ± 3.3500 in Group 3. Our findings demonstrate that haemoglobin, red blood cell count, platelet count, and liver enzyme levels (AST and ALT) decrease as CKD progresses while white blood cell count increases. These insights into haematological and hepatic biomarkers underscore the dynamic nature of CKD pathology and may inform clinical management strategies.
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