Comparison of Serum Holotranscobalamin with Serum Vitamin B12 in Population Prone to Megaloblastic Anemia and their Correlation with Nerve Conduction Study.

IF 1.5 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Indian Journal of Clinical Biochemistry Pub Date : 2023-01-01 Epub Date: 2022-03-17 DOI:10.1007/s12291-022-01027-x
Abhishek Verma, Sunita Aggarwal, Sandeep Garg, Smita Kaushik, Debashish Chowdhury
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Abstract

Early detection of megaloblastic anemia and associated neurological complications is crucial for management. This study was conducted to compare serum holotranscobalamin level with serum vitamin B12 level as early biomarker in people prone to megaloblastic anemia and to evaluate co-relation between these biomarkers and nerve conduction study in study patients. 83 adult patients (Hb > 12 gm/dl) prone to megaloblastic anemia were studied for basic haematological investigations, random blood sugar, thyroid function test, liver function test, kidney function test, serum vitamin B12, serum holotranscobalamin and serum folic acid levels. 45 patients among them underwent nerve conduction studies. All study patients were classified in 6 groups on the basis of risk factors for megaloblastic anemia. 29 patients (34.9%) were on antiepileptic drugs, 26 (31.3%) were chronic alcoholic, 10 patients (12%) each, had malabsorption and ileal tuberculosis, 6 (7.22%) had chronic pancreatitis and 2 (2.4%) had ileal resection. 30 patients (36.14%) had low serum holotranscobalamin, including 7 patients (8.43%) with low serum vitamin B12 level also, unmasking vitamin B12 deficiency in 23 patients (27.7%). 7 patients (8.43%) had mean corpuscular volume (MCV) > 100fL and 8 patients (9.63%) had vitamin B12 deficiency related changes on peripheral smear. Serum vitamin B12 and holotranscobalamin levels were significantly low in patients with peripheral smear changes, with p value 0.039 and 0.041 respectively, while no such association seen with MCV. Subclinical peripheral neuropathy was detected in 18 (40%) out of 45 patients on nerve conduction study. Serum holotranscobalamin levels were significantly lower (p = 0.031) than serum vitamin B12 levels (p = 0.2) in patients with neuropathic changes. Rest investigations and serum folic acid levels were normal in all patients. Holotranscobalamin levels can be considered early and reliable marker for vitamin B12 deficiency and deficiency associated peripheral neuropathy, even in patients who are prone to megaloblastic anemia, and not yet anemic or symptomatic for neuropathy.

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易患巨幼红细胞性贫血人群血清全曲钴胺与血清维生素 B12 的比较及其与神经传导研究的相关性。
早期发现巨幼细胞性贫血及相关神经系统并发症对于治疗至关重要。本研究旨在比较血清全转铁蛋白水平和血清维生素 B12 水平作为巨幼细胞性贫血患者的早期生物标志物,并评估这些生物标志物与患者神经传导研究之间的相关性。研究人员对 83 名易患巨幼细胞性贫血的成年患者(血红蛋白大于 12 克/分升)进行了基本血液学检查、随机血糖、甲状腺功能检测、肝功能检测、肾功能检测、血清维生素 B12、血清全转铁蛋白和血清叶酸水平检测。其中 45 名患者接受了神经传导检查。根据巨幼细胞贫血的风险因素,所有研究对象被分为 6 组。29名患者(34.9%)服用过抗癫痫药物,26名患者(31.3%)长期酗酒,10名患者(12%)患有吸收不良和回肠结核,6名患者(7.22%)患有慢性胰腺炎,2名患者(2.4%)进行过回肠切除术。30 名患者(36.14%)的血清全转录钴胺素水平较低,其中 7 名患者(8.43%)的血清维生素 B12 水平也较低,23 名患者(27.7%)的维生素 B12 缺乏。7 名患者(8.43%)的平均血球容积(MCV)大于 100fL,8 名患者(9.63%)的外周涂片出现与维生素 B12 缺乏相关的变化。有外周涂片变化的患者血清维生素 B12 和全血钴胺素水平明显偏低,P 值分别为 0.039 和 0.041,而 MCV 与维生素 B12 缺乏症无关联。45 名患者中有 18 人(40%)在神经传导检查中发现了亚临床周围神经病变。在有神经病变的患者中,血清全曲钴胺素水平(p = 0.031)明显低于血清维生素 B12 水平(p = 0.2)。所有患者的其他检查和血清叶酸水平均正常。即使是易患巨幼红细胞性贫血、尚未贫血或没有神经病变症状的患者,全血钴胺水平也可被视为维生素 B12 缺乏症和缺乏症相关周围神经病变的早期可靠标志物。
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来源期刊
Indian Journal of Clinical Biochemistry
Indian Journal of Clinical Biochemistry BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
4.50
自引率
4.80%
发文量
74
期刊介绍: The primary mission of the journal is to promote improvement in the health and well-being of community through the development and practice of clinical biochemistry and dissemination of knowledge and recent advances in this discipline among professionals, diagnostics industry, government and non-government organizations. Indian Journal of Clinical Biochemistry (IJCB) publishes peer reviewed articles that contribute to the existing knowledge in all fields of Clinical biochemistry, either experimental or theoretical, particularly deal with the applications of biochemistry, molecular biology, genetics, biotechnology, and immunology to the diagnosis, treatment, monitoring and prevention of human diseases. The articles published also include those covering the analytical and molecular diagnostic techniques, instrumentation, data processing, quality assurance and accreditation aspects of the clinical investigations in which chemistry has played a major role, or laboratory animal studies with biochemical and clinical relevance.
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