糖化血红蛋白在非糖尿病患者诊断为良性甲状腺病变细胞学:横断面研究从三级保健中心在印度

Reetika Menia
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引用次数: 1

摘要

背景:甲状腺功能减退和糖尿病通常共存,是印度最常见的内分泌疾病(1)。糖化血红蛋白(HbA1c)用于评估血糖,美国糖尿病协会(ADA)建议将其用于糖尿病和糖尿病前期(2)。糖化血红蛋白(HbA1c)的值在5.7%至6.5%之间代表糖尿病前期,而值≥6.5%被认为是糖尿病(3)。糖化血红蛋白是血红蛋白的一部分,在循环寿命期间经历非酶糖化红细胞(4)。一些研究表明,糖化Hb在不同的情况下,如血红蛋白病、妊娠和慢性肾病(5)。甲状腺激素在葡萄糖稳态中起重要作用(6)。TSH调节骨髓造血(7)。甲状腺功能减退症抑制骨髓,导致红细胞生成减少,改变红细胞的寿命。寿命的改变导致HbA1C的虚假升高(8,9,10)。因此,糖化Hb不仅取决于血糖,还取决于红细胞的寿命(11)。影响红细胞周转或存活的条件导致Hb A1C水平虚高或虚低(12)。红细胞周转在甲状腺中毒状态下增加,而甲状腺功能减退则有相反的效果(3)。在本研究中,我们假设糖化血红蛋白在甲状腺状态改变的个体中表现出差异。它还旨在确定甲状腺状态改变患者的空腹血糖水平与糖化血红蛋白之间是否存在相关性。目的:寻找细胞学诊断为良性甲状腺病变的非糖尿病患者甲状腺特征与糖化血红蛋白之间的相关性,并比较这些患者的空腹血糖和血红蛋白与糖化血红蛋白之间的关系。材料和方法:经伦理委员会同意,对法里达巴德ESIC医学院和医院病理科细胞学诊断为甲状腺良性病变的50例患者进行横断面研究。数据分析:采用Pearson’s系数检验变量间的相关性。显著性水平设为5%。结果:50例患者中(n=25) 50%甲状腺功能减退,(n=13) 26%甲状腺功能亢进,(n=12) 24%甲状腺功能正常,(n=22) 88% HbA1C >6.5%的甲状腺功能减退患者被标记为糖尿病,(n=3) 12%甲状腺功能减退患者被标记为糖尿病前期,无非糖尿病。大部分甲状腺功能正常(n=11)的患者(92%)和所有甲状腺功能亢进(n=13)的患者(100%)的HbA1C在非糖尿病6.5%范围内。HbA1C与TSH、Hb、MCH或糖尿病前期(HbA1C在5.7 ~ 6.5%之间)的相关性均有统计学意义(p < 6.5%)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glycosylated Hemoglobin among Non-diabetic Patients Diagnosed as Benign Thyroid Lesions on Cytology: A Cross Sectional Study from a Tertiary Care Centre in India
Background: Hypothyroidism and diabetes usually coexist and are the most common endocrine disorders seen in India (1). Glycosylated Hb (HbA1c) is used for assessment of glycemia and American Diabetic Association (ADA) has recommended its use in diabetes and prediabetes (2). A value between 5.7% and 6.5% represents prediabetes while a value ≥6.5% is considered as diabetes mellitus (3). Glycosylated hemoglobin is a fraction of hemoglobin that undergoes non-enzymatic glycation over the circulatory life span of erythrocytes (4). Several studies have shown glycosylated Hb varies in different conditions like hemoglobinopathies, pregnancy and chronic kidney disease (5). Thyroid hormone plays an important role in glucose homeostasis (6). TSH regulates hematopoiesis in bone marrow (7). Hypothyroidism depresses the marrow which causes decreased erythrocyte production which alters the life span of erythrocytes. Altered life span causes spurious elevation of HbA1C (8, 9, 10). Hence, glycosylated Hb not only depends on glycemia but also on life span of RBC (11). Conditions which effect erythrocyte turnover or survival lead to falsely high or low Hb A1C levels (12). RBC turnover is increased in thyrotoxic states whereas hypothyroidism has the opposite effect (3). In the present study, we hypothesise that glycosylated hemoglobin shows variation in individuals with altered thyroid status. It also aim to establish if a correlation exits between fasting plasma glucose level and hemoglobin with glycosylated hemoglobin in patients with altered thyroid status. Aims and Objectives: To find a correlation between thyroid profile and glycosylated Hb in non-diabetic patients who have been diagnosed on cytology as benign thyroid lesions and Compare the fasting blood glucose and hemoglobin with glycosylated Hb in these patients. Material and Methods: A cross sectional study on 50 cases cytologically diagnosed as benign thyroid lesions in the Department of Pathology in ESIC Medical College and Hospital Faridabad were included in the study with consent of ethical committee. Data Analysis: Pearson’s coefficient was applied to test the association between variables. The significance level was set at 5%. Results: Out of 50 patients (n=25) 50% were hypothyroid, (n=13) 26% were hyperthyroid and (n=12) 24% were euthyroid and (n=22) 88% hypothyroid patients presented with HbA1C >6.5% and were labeled as Diabetic, (n=3) 12% hypothyroid patients were labelled as prediabetic and none was nondiabetic. Most of the euthyroid (n=11) 92% and all of the hyperthyroid patients (n=13) 100% had HbA1C in the nondiabetic range of 6.5%). The correlation of HbA1C with TSH, Hb and MCH of these patients showed statistical significance (p 6.5%) or prediabetic (HbAIc between 5.7 to 6.5%).
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