A Case of Functional Adrenal Insufficiency Secondary to COVID-19 Infection

M. A. Ahmed, C. Sun, A. Mohan, D. Djondo
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Abstract

Since the outbreak of the Coronavirus Disease 2019 (COVID-19) pandemic, over seventy million cases have been reported worldwide. Patients present with various symptoms, including extra-pulmonary manifestations. However, manifestations on adrenal glands have not been reported extensively. Here, we present a case of functional adrenal insufficiency in a COVID-19 patient. A 61-year-old male with a history of hyperlipidemia presented with fatigue, cough, and dyspnea, subsequently tested positive for COVID-19. His blood pressure (BP) on admission was 128/68 mmHg with 86% oxygen saturation on room air. Dexamethasone 6mg daily was started for ten days. Remdesivir was contra-indicated, considering the ALT of 246 and AST of 248. On day seven of hospitalization, he had progressively worsening respiratory symptoms and was transferred to the Intensive Care Unit with BP of 105/63 mmHg. Within 48 hours, he showed positive orthostatic vitals with BP of 85/54 mmHg. Despite intravenous hydration, his BP was consistently low on subsequent days with 88/53 mmHg and 99/66 mmHg. His serum total cortisol level was 9.2 μg/dL, and he showed a positive response to IV Hydrocortisone 50mg as well as oral prednisone 10 mg the following day. We did not obtain a cosyntropin stimulation test because of recent corticosteroid therapy. Midodrine 2.5mg three times daily (TID) was started, then increased to 10 mg to maintain BP and alleviate orthostatic symptoms. However, symptomatic positive orthostatic vitals were persistent. He was discharged on midodrine 7.5 mg TID and Fludrocortisone 0.1 mg daily for suspicion of functional adrenal insufficiency. Additionally, a HDL level of 22 mg/dL was recorded (vs 56 mg/dL six months ago). At three months follow-up, he was off fludrocortisone and midodrine with improved orthostatic symptoms. Hypotension and orthostatic symptoms in COVID-19 could be due to IL-1, IL-6, or tumor necrosis factor-mediated reduction in ACTH secretion. Acute illnesses, including COVID-19, may also increase cortisol demand, causing adrenal insufficiency. Decreased HDL noted in our patient could be another etiology. "Critical Illness-Related Corticosteroid Insufficiency" (CIRCI) is a functional adrenal insufficiency that is not strictly dependent on cortisol level for diagnosis but mostly on the inadequacy of cortisol for inflammation control or supplying the raised metabolic demand. Decreased cortisol complex cleavage, increased activity of an enzyme responsible for cortisol inactivation, and decreased numbers and affinity of cortisol receptors were postulated to play a role. Therefore, adrenal insufficiency as a cause of hypotension following COVID-19 infection should not be overlooked despite normal cortisol levels.
COVID-19感染继发功能性肾上腺功能不全1例
自2019冠状病毒病(COVID-19)大流行爆发以来,全球已报告7000多万例病例。患者表现出各种症状,包括肺外表现。然而,肾上腺的表现尚未被广泛报道。在此,我们报告一例COVID-19患者的功能性肾上腺功能不全。61岁男性,有高脂血症病史,表现为疲劳、咳嗽和呼吸困难,随后COVID-19检测呈阳性。入院时血压(BP)为128/68 mmHg,室内空气氧饱和度为86%。地塞米松每日6mg,连用10天。考虑到ALT 246和AST 248, Remdesivir是禁忌适应症。住院第7天,患者呼吸道症状逐渐恶化,血压为105/63 mmHg,转至重症监护病房。48小时内,他的直立性生命体征呈阳性,血压为85/54 mmHg。尽管静脉补水,他的血压在随后的几天持续较低,分别为88/53 mmHg和99/66 mmHg。患者血清总皮质醇水平为9.2 μg/dL,静脉注射氢化可的松50mg,第二天口服强的松10mg,均呈阳性反应。由于最近的皮质类固醇治疗,我们没有进行共syntropin刺激试验。开始使用米多德林2.5mg,每日3次(TID),随后增加至10 mg,以维持血压和缓解直立症状。然而,症状阳性的直立性生命体征持续存在。因怀疑肾上腺功能不全,每日给予米多宁7.5 mg TID和氟化可的松0.1 mg。此外,高密度脂蛋白水平为22 mg/dL(六个月前为56 mg/dL)。随访3个月,停用氟可的松和米多宁,直立性症状得到改善。COVID-19患者的低血压和直立症状可能是由于IL-1、IL-6或肿瘤坏死因子介导的ACTH分泌减少所致。包括COVID-19在内的急性疾病也可能增加皮质醇需求,导致肾上腺功能不全。本例患者HDL降低可能是另一个病因。“重症相关皮质类固醇功能不全”(CIRCI)是一种功能性肾上腺功能不全,其诊断并不严格依赖于皮质醇水平,而主要取决于皮质醇不足以控制炎症或供应升高的代谢需求。皮质醇复合体切割减少,皮质醇失活酶活性增加,皮质醇受体数量和亲和力减少被认为起作用。因此,尽管皮质醇水平正常,但不应忽视肾上腺功能不全作为COVID-19感染后低血压的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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