Gender-driven thyroid dysfunction in systemic lupus erythematosus patients: Clinical significance of an overlooked association and global stance

IF 1 Q4 RHEUMATOLOGY
Ibtisam M.A. Jali
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Abstract

Aim of the work

This study aimed to determine the association of thyroid dysfunction in systemic lupus erythematosus (SLE) patients.

Patients and methods

Out of a cohort including 312 adult SLE patients those with thyroid dysfunction (n = 53) were further evaluated. The medical history, clinical examination, laboratory investigations and medications received were recorded. The SLICC damage index (SLICC-DI) was assessed.

Results

Thyroid dysfunction formed 17 % of the patients and their mean age was 39.5 ± 11.5 years and disease duration 5.6 ± 3.3 years were comparable to those without thyroid disorder, however female gender was predominantly higher (F:M 52:1 vs 6.2:1, p < 0.0001). The frequency of thyroid dysfunction was alike in Saudi (16 %) and non-Saudi (17.9 %) patients (p = 0.66). The majority of cases (96.2 %) had hypothyroidism, one with autoimmune thyroiditis, while only 2 (3.8 %) had hyperthyroidism. There was a significantly increased frequency of associated neuropsychiatric manifestations (64.2 % vs 45.2 %;p = 0.012), and hematological involvement (32.1 % vs 14.3 %; p = 0.011) and less complement (C4) consumption (15.1 % vs 23.6 %; p = 0.048) in those with thyroid dysfunction compared to those without. The frequency of anti-double stranded deoxyribonucleic acid (anti-dsDNA) positivity tended to be higher (71.7 % vs 66.8 %) and its titre significantly lower (316.3 ± 319.8 IU/ml vs 461.3 ± 459.1; p = 0.013). The SLICC-DI and mortality rate were comparable between groups. Only the presence of proteinuria inversely significantly correlated with the level of T4 (r = -0.31, p = 0.007).

Conclusion

Thyroid dysfunction forms a notable percentage of SLE patients with a prominent female gender propensity. The significant relation of thyroid disorders to neuropsychiatric manifestations, hematological involvement, C4 consumption and anti-dsDNA deserves recognition.

系统性红斑狼疮患者中由性别驱动的甲状腺功能障碍:被忽视的关联和全球立场的临床意义
这项研究旨在确定系统性红斑狼疮(SLE)患者甲状腺功能障碍的相关性。患者和方法在包括312名成年系统性红斑狼疮患者的队列中,对甲状腺功能障碍患者(53人)进行了进一步评估。病史、临床检查、实验室检查和接受的药物均被记录在案。结果甲状腺功能障碍患者占17%,平均年龄为(39.5 ± 11.5)岁,病程为(5.6 ± 3.3)年,与无甲状腺功能障碍的患者相当,但女性患者居多(女:男52:1 vs 6.2:1,p < 0.0001)。沙特籍(16%)和非沙特籍(17.9%)患者的甲状腺功能障碍发生率相同(p = 0.66)。大多数病例(96.2%)患有甲状腺功能减退症,其中一人患有自身免疫性甲状腺炎,只有两人(3.8%)患有甲状腺功能亢进症。与无甲状腺功能障碍的病例相比,有甲状腺功能障碍的病例出现相关神经精神症状(64.2% vs 45.2%;P = 0.012)、血液病(32.1% vs 14.3%;P = 0.011)和补体(C4)消耗较少(15.1% vs 23.6%;P = 0.048)的频率明显增加。抗双链脱氧核糖核酸(anti-dsDNA)阳性的频率往往更高(71.7% vs 66.8%),滴度明显更低(316.3 ± 319.8 IU/ml vs 461.3 ± 459.1;p = 0.013)。各组的 SLICC-DI 和死亡率相当。结论甲状腺功能障碍在系统性红斑狼疮患者中占有相当大的比例,且女性患者占多数。甲状腺功能紊乱与神经精神表现、血液学受累、C4消耗和抗dsDNA的重要关系值得肯定。
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来源期刊
Egyptian Rheumatologist
Egyptian Rheumatologist RHEUMATOLOGY-
CiteScore
2.00
自引率
22.20%
发文量
77
审稿时长
39 weeks
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