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意料之外的风湿科基因检测高需求:一项横断面队列研究。

Unexpected High Need for Genetic Testing in Rheumatology: A Cross-Sectional Cohort Study.

机构信息

Department of Internal Medicine, Clinic II, Medical University of Innsbruck, 6020 Innsbruck, Austria.

出版信息

Genes (Basel). 2023 Sep 24;14(10):1858. doi: 10.3390/genes14101858.

Abstract

BACKGROUND

Genetic testing may provide information for diagnostic, prognostic and pharmacogenetic purposes. The PREPARE study recently showed that the number of clinically relevant adverse drug reactions could be reduced via genotype-guided treatment. The aim of this work was to assess the relevance of genetic testing and its actual use in consecutive rheumatic outpatients.

METHODS

A retrospective cross-sectional analysis was performed with data from a prospectively designed observational project with outpatients consecutively recruited from a university clinic of rheumatology.

RESULTS

In this cohort of 2490 patients, the potential need for genetic testing is immense, with 57.3% of patients having the potential to benefit from genetic testing according to their diagnosis and treatment and 53.3% of patients with actually performed genetic testing for diagnostic, prognostic or pharmacogenetic purposes. In detail, patients would potentially benefit from genetic testing especially for therapeutic (28.0%) and diagnostic (26.9%) purposes. Genetic testing was performed for diagnostic purposes in 51.6% of subjects, for pharmacogenetic purposes in 3.7% and for prognostic purposes in 0.1%. The ratio between the number of patients who had had tests performed to those with a potential need for genetic testing decreased with age, from 127.1% for 20 to <30-year-old patients to 46.1% for 80 to <90-year-old patients. Pharmacogenetic testing was only performed for disease-related medications.

CONCLUSIONS

Genetic testing is frequently needed in patients with rheumatic diseases. The value of pharmacogenetic testing is certainly underestimated, especially in case of medications for comorbidities.

摘要

背景

基因检测可为诊断、预后和药物遗传学目的提供信息。最近的 PREPARE 研究表明,通过基因型指导治疗可以减少临床相关的药物不良反应数量。本研究旨在评估遗传检测的相关性及其在连续风湿科门诊患者中的实际应用。

方法

对一项前瞻性设计的观察性项目进行回顾性横断面分析,该项目连续招募了一家大学风湿病诊所的门诊患者。

结果

在这个 2490 名患者的队列中,基因检测的潜在需求巨大,根据诊断和治疗,57.3%的患者可能受益于基因检测,53.3%的患者实际上进行了基因检测,用于诊断、预后或药物遗传学目的。具体来说,患者尤其可能受益于基因检测,用于治疗(28.0%)和诊断(26.9%)目的。51.6%的患者进行了基因检测以明确诊断,3.7%的患者进行了药物遗传学检测,0.1%的患者进行了预后检测。进行了检测的患者数量与有基因检测需求的患者数量之比随着年龄的增长而降低,从 20 至<30 岁患者的 127.1%降至 80 至<90 岁患者的 46.1%。药物遗传学检测仅针对与疾病相关的药物进行。

结论

风湿性疾病患者经常需要基因检测。药物遗传学检测的价值肯定被低估了,特别是在治疗合并症的药物方面。

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