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对大量血清肌酸激酶水平升高但无症状或症状轻微的患者进行的回顾性研究。

Retrospective study of a large population of patients with asymptomatic or minimally symptomatic raised serum creatine kinase levels.

作者信息

Prelle Alessandro, Tancredi Lucia, Sciacco Monica, Chiveri Luca, Comi Giacomo P, Battistel Alessandro, Bazzi Paola, Martinelli Boneschi Filippo, Bagnardi Vincenzo, Ciscato Patrizia, Bordoni Andreina, Fortunato Franco, Strazzer Sandra, Bresolin Nereo, Scarlato Guglielmo, Moggio Maurizio

机构信息

Istituto di Clinica Neurologica, Ospedale Maggiore IRCCS, Milano, Italy.

出版信息

J Neurol. 2002 Mar;249(3):305-11. doi: 10.1007/s004150200010.

Abstract

UNLABELLED

A retrospective evaluation of asymptomatic subjects with persistent elevation of serum creatine kinase (CK) levels (hyperCKemia) was made in order to verify the presence of subclinical myopathy or idiopathic hyperCKemia and to define the most appropriate diagnostic pathway. Persistently increased serum CK levels are occasionally encountered in healthy individuals. In 1980 Rowland coined for them the term idiopathic hyperCKemia. Despite the increase of scientific knowledge, several healthy subjects with hyperCKemia still represent a problem for the clinician. We made a retrospective evaluation of 114 asymptomatic or minimally symptomatic individuals with incidentally detected persistent hyperCKemia. They underwent neurological examination and laboratory/instrumental evaluation. Skeletal muscle biopsy was performed and thoroughly investigated. Biochemical and genetic investigations were added in selected cases. Logistic regression analysis was applied. We diagnosed a neuromuscular disorder in 21 patients (18.4%), and found, by muscle biopsy and/or EMG, pathological but not conclusive findings in 57 subjects (50%). The statistic correlation between elevated serum CK levels and the probability of making a diagnosis changed according to the age of the patient.

CONCLUSIONS

Muscle biopsy is the basic tool for screening asymptomatic subjects with hyperCKemia. It allowed us to make a diagnosis of disease in 18.4% of patients, and to detect skeletal muscle abnormalities in 38.6% of the subjects. Interestingly, 31.6% of individuals had completely normal muscle findings. These best fit the "diagnosis" of idiopathic hyperCKemia.

摘要

未标注

为了验证亚临床肌病或特发性高肌酸激酶血症的存在,并确定最合适的诊断途径,对血清肌酸激酶(CK)水平持续升高(高CK血症)的无症状受试者进行了回顾性评估。健康个体偶尔会出现血清CK水平持续升高的情况。1980年,罗兰为其创造了“特发性高CK血症”这一术语。尽管科学知识有所增加,但对于临床医生来说,仍有一些高CK血症的健康受试者是个难题。我们对114例偶然发现持续性高CK血症的无症状或症状轻微的个体进行了回顾性评估。他们接受了神经系统检查以及实验室/仪器评估。进行了骨骼肌活检并进行了全面研究。在选定病例中增加了生化和基因检测。应用了逻辑回归分析。我们在21例患者(18.4%)中诊断出神经肌肉疾病,通过肌肉活检和/或肌电图检查,在57名受试者(50%)中发现了病理性但非决定性的结果。血清CK水平升高与诊断概率之间的统计相关性因患者年龄而异。

结论

肌肉活检是筛查高CK血症无症状受试者的基本工具。它使我们能够在18.4%的患者中做出疾病诊断,并在38.6%的受试者中检测到骨骼肌异常。有趣的是,31.6%的个体肌肉检查结果完全正常。这些最符合特发性高CK血症的“诊断”。

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