先天性纤维蛋白原不良血症中的甲状腺功能检测误区。

IF 2.1 4区 医学 Q3 MEDICAL LABORATORY TECHNOLOGY
Annals of Clinical Biochemistry Pub Date : 2024-11-01 Epub Date: 2024-06-20 DOI:10.1177/00045632241263494
Angela D Burns, Christina Kanonidou, Jane McNeilly
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引用次数: 0

摘要

潜伏纤维蛋白凝块的存在是公认的导致免疫测定结果不准确的分析前因素。本报告详细介绍了一例患有巴塞杜氏病和先天性纤维蛋白原血症(CD)的患者,其血清甲状腺功能检测(TFT)结果与临床体征或症状不符。对患者血浆样本的分析结果比血清样本更准确。报告还描述了其他 CD 患者的病例,这些患者都有相同的纤维蛋白原基因突变,但 TFT 却不一致,在这些病例中,血清样本中的 TFT 测量结果并不可靠。尽管有证据表明纤维蛋白会影响免疫测定,但这是第一份将 CD 与免疫测定结果错误联系起来的同类报告。据推测,其机制与纤维蛋白原的非典型形式有关,导致血清样本中的潜伏纤维蛋白阻塞抗原结合位点,从而导致错误结果。大多数患者无症状,因此 TFT 异常(尽管不准确)可能是首次发现。在解释 TFT 时,必须认识到 CD 是导致结果不一致的原因之一,以避免对患者进行不必要的检查和不适当的临床干预,并有可能发现未确诊的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Misleading thyroid function tests in congenital dysfibrinogenemia.

The presence of latent fibrin clots is a recognised pre-analytical factor that causes inaccurate immunoassay results. This report details a case of a patient with Graves' disease and congenital dysfibrinogenemia (CD) that had serum thyroid function test results (TFTs) that were not in keeping with clinical signs or symptoms. Analysis of plasma samples taken from the patient was shown to provide more accurate results than those obtained using serum samples. Further cases of patients with CD, all sharing the same genetic mutation of fibrinogen, and discordant TFTs are described, where TFTs measurement in serum samples proved to be unreliable. Despite evidence of fibrin effecting immunoassays, this is the first report of its kind linking CD to erroneous immunoassay results. The mechanism is postulated to be related to atypical forms of fibrinogen resulting in latent fibrin in serum samples blocking the antigen binding site and leading to incorrect results. Congenital dysfibrinogenemia is asymptomatic in most patients and therefore abnormal, albeit inaccurate, TFTs may be the first finding. Recognition of CD as a cause of discordant results is important when interpreting TFTs to avoid unnecessary investigations and inappropriate clinical interventions to those with the disorder and potentially identify undiagnosed cases.

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来源期刊
Annals of Clinical Biochemistry
Annals of Clinical Biochemistry Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
5.20
自引率
4.50%
发文量
61
期刊介绍: Annals of Clinical Biochemistry is the fully peer reviewed international journal of the Association for Clinical Biochemistry and Laboratory Medicine. Annals of Clinical Biochemistry accepts papers that contribute to knowledge in all fields of laboratory medicine, especially those pertaining to the understanding, diagnosis and treatment of human disease. It publishes papers on clinical biochemistry, clinical audit, metabolic medicine, immunology, genetics, biotechnology, haematology, microbiology, computing and management where they have both biochemical and clinical relevance. Papers describing evaluation or implementation of commercial reagent kits or the performance of new analysers require substantial original information. Unless of exceptional interest and novelty, studies dealing with the redox status in various diseases are not generally considered within the journal''s scope. Studies documenting the association of single nucleotide polymorphisms (SNPs) with particular phenotypes will not normally be considered, given the greater strength of genome wide association studies (GWAS). Research undertaken in non-human animals will not be considered for publication in the Annals. Annals of Clinical Biochemistry is also the official journal of NVKC (de Nederlandse Vereniging voor Klinische Chemie) and JSCC (Japan Society of Clinical Chemistry).
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