Spectrum of Thyroid Dysfunction in Patients with Chronic Kidney Disease in Benin City, Nigeria.

John O Obasuyi, Mathias A Emokpae
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Abstract

There is an indication of abrupt rise in chronic kidney disease (CKD) in Nigeria and thyroid function involvement has not been sufficiently evaluated. This study determined thyroid gland function among subjects with CKD in Benin City, Nigeria. A total of 184 randomized CKD patients attending specialist clinic and 80 healthy control subjects were recruited for this study. A well-structured questionnaire was used to obtain data on socio-demography. Blood specimens were collected and used for the determination of thyroid function parameters; thyroid stimulating hormone (TSH), triiodothyronine (T3), free triiodothyronine (fT3), thyroxine (T4), free thyroxine (fT4), thyroid peroxidase antibody (TPO-Abs), thyroid globulin antibody (Tg-Abs) and Deiodinase enzyme Type 1 (D1). SPINA GD and SPINA GT were calculated using Michaelis-Menten model. The CKD was classified into stages using Modification of Drug in Renal Disease (MDRD) formula. Thyroid dysfunctions observed were clinical hyperthyroidism 1 (0.54%), non-thyroidal illness 78 (42.4%), clinical hypothyroidism 11 (6.0%), sub-clinical hyperthyroidism 3 (1.60%), and sub-clinical hypothyroidism 11 (6.0%), while euthyroid were 80 (43.5%). SPINA GD of CKD patients (33.85 ± 10.94) was not significantly different when compared with controls (24.85 ± 1.57), whereas, SPINA GT was significantly higher (p < 0.01) among CKD patients (3.74 ± 0.31) than controls (2.68 ± 0.11). Autoimmune thyroid disease demonstrated by positive Tg-Abs and TPO-Abs were observed among approximately 7.9% of CKD patients. Serum TPO-Abs concentration increased with CKD progression. Thyroid dysfunction is involved in the pathogenesis of CKD patients. The etiologies are multifactorial and immunological mechanisms of autoimmune thyroid disease may be a contributing factor.

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尼日利亚贝宁市慢性肾病患者甲状腺功能障碍谱
有迹象表明,尼日利亚慢性肾脏疾病(CKD)突然上升,甲状腺功能的影响尚未得到充分评估。本研究测定了尼日利亚贝宁市慢性肾病患者的甲状腺功能。本研究共随机招募184名专科门诊CKD患者和80名健康对照者。一份结构良好的调查问卷用于获取社会人口统计数据。采集血液标本,测定甲状腺功能参数;促甲状腺激素(TSH)、三碘甲状腺原氨酸(T3)、游离三碘甲状腺原氨酸(fT3)、甲状腺素(T4)、游离甲状腺素(fT4)、甲状腺过氧化物酶抗体(TPO-Abs)、甲状腺球蛋白抗体(Tg-Abs)和去碘酶1型(D1)。SPINA GD和SPINA GT采用Michaelis-Menten模型计算。采用肾脏疾病药物改良(MDRD)配方对CKD进行分期。甲状腺功能障碍为临床甲亢1型(0.54%)、非甲状腺疾病78型(42.4%)、临床甲减11型(6.0%)、亚临床甲亢3型(1.60%)、亚临床甲减11型(6.0%),甲状腺功能正常80例(43.5%)。CKD组SPINA GD值(33.85±10.94)与对照组(24.85±1.57)差异无统计学意义,而CKD组SPINA GT值(3.74±0.31)显著高于对照组(2.68±0.11),差异有统计学意义(p < 0.01)。在约7.9%的CKD患者中观察到以Tg-Abs和TPO-Abs阳性为表现的自身免疫性甲状腺疾病。血清TPO-Abs浓度随CKD进展而升高。慢性肾病的发病机制与甲状腺功能障碍有关。其病因是多因素的,自身免疫性甲状腺疾病的免疫机制可能是一个促成因素。
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