伊洛林市艾滋病毒抗体阴性的 2 型糖尿病患者 CD4+ T 细胞计数偏低的情况

Ilesanmi Ayodele O, Atanda Tiamiyu A, Ilesanmi Rose, Ogunniyi Tolulope J, Akinleye Waheed A
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摘要

背景和目的:糖尿病(DM)是一种代谢紊乱性疾病,表现为慢性高血糖,同时伴有碳水化合物、脂类和蛋白质代谢障碍。一些研究早前已经指出了与该疾病相关的几种并发症,尤其是患者对各种传染病的易感性。因此,我们试图通过评估 DM 患者的 CD4+ T 细胞数量,来研究这种疾病的适应性免疫状态。研究方法研究招募了 76 名 2 型糖尿病患者。三十(30)名年龄和性别匹配的非糖尿病患者作为阴性对照。他们的空腹血糖(FBS)、糖化血红蛋白(HbA1c)和 CD4 细胞计数均采用标准化程序进行检测。比较了研究组和对照组在年龄、性别、体重指数、FBS、HbA1c 和 CD4+ T 细胞计数方面的人口统计学和临床数据。研究结果与对照组(3.67 ± 0.66)(P = 0.0001)和(5.20 ± 0.48)(P = 0.0001)相比,DM 患者的葡萄糖平均浓度(7.82 ± 2.58)和 HBA1c 百分比浓度(8.21 ± 2.31)均显著升高。与对照组(1067.9 ± 195.4)相比,DM 受试者的 CD4+ 细胞计数(843.58 ± 297.6)也明显较低(p = 0.035)。结论在我们的研究中发现,糖尿病患者的 CD4+ T 细胞水平明显下降,这可能是导致糖尿病相关并发症加重的一个因素,尤其是那些易感染的疾病。我们发现,在糖尿病患者中,Hb-AA 与 CD4+ T 细胞正常或升高有关;而 Hb-AS 变异则会增加 CD4+ T 细胞计数偏低的几率。CD4+T细胞计数评估应作为DM患者定期检查的一部分,尤其是那些尽管接受了治疗但并发症仍未得到解决的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low CD4+ T Cell count among HIV-seronegative Type 2 Diabetes Mellitus patients in Ilorin metropolis
Background and aims: Diabetes Mellitus (DM) is a metabolic disorder that manifests as chronic hyperglycemia accompanied by a dysfunctional metabolism of carbohydrates, lipids, and proteins. Several studies have earlier pointed out several complications associated with the disease and in particular, the sufferer’s susceptibility to various infectious diseases. We therefore sought to investigate the adaptive immune status of the condition, as represented by the assessment of CD4+ T cell count among DM patients. Method: Seventy-six type 2 DM patients were recruited for the study. Thirty (30) age and sex-matched, non-diabetic individuals were enrolled as negative controls. Their fasting blood sugar (FBS), HbA1c, and CD4 count were assayed using standardized procedures. The demographic and clinical data of the studied group and controls were compared with respect to age, sex, BMI, FBS, HbA1c, and CD4+ T cell counts. Result: The mean concentration of glucose (7.82 ± 2.58) and the percentage concentration of HBA1c (8.21 ± 2.31) were significantly higher in DM individuals as against the control (3.67 ± 0.66) (p = 0.0001) and (5.20 ± 0.48) (p = 0.0001) respectively. The CD4+ cell count was also significantly lower in DM subjects (843.58 ± 297.6) when compared with the control (1067.9 ±195.4) (p = 0.035). Conclusion: A significant reduction in CD4+ T cell level was noted among diabetic patients in our study, which could be a contributing factor for aggravating some of the associated complications in DM, especially those that involve susceptibility to infectious diseases. We found out that having Hb-AA is associated with normal or elevated CD4+ T cells in DM patients; whereas having the Hb-AS variant increases the chance of a low CD4+ T cell count. Assessment of CD4+ T cell count should be included as part of periodic investigations in DM patients, especially for those with unresolved complications, in spite of treatment.
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