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中国科学技术大学附属第一医院(安徽省立医院)药学部,合肥 230001
主管药师,硕士。研究方向:医院药学。E-mail:dmyhf@163.com
主任药师,博士生导师,博士。研究方向:医院药学。E-mail:tangliqin@ustc.edu.cn
收稿:2025-08-29,
修回:2025-10-27,
录用:2025-11-17,
纸质出版:2025-12-30
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邓明影,杨本军,冯晓俊,等.HLA-B*15:02阴性患者发生抗癫痫药物相关严重皮肤不良反应的非遗传风险因素研究 Δ[J].中国药房,2025,36(24):3091-3095.
DENG Mingying,YANG Benjun,FENG Xiaojun,et al.Study on non-genetic risk factors for antiepileptic drug-induced severe cutaneous adverse reactions in HLA-B*15:02 negative patients[J].ZHONGGUO YAOFANG,2025,36(24):3091-3095.
邓明影,杨本军,冯晓俊,等.HLA-B*15:02阴性患者发生抗癫痫药物相关严重皮肤不良反应的非遗传风险因素研究 Δ[J].中国药房,2025,36(24):3091-3095. DOI: 10.6039/j.issn.1001-0408.2025.24.13.
DENG Mingying,YANG Benjun,FENG Xiaojun,et al.Study on non-genetic risk factors for antiepileptic drug-induced severe cutaneous adverse reactions in HLA-B*15:02 negative patients[J].ZHONGGUO YAOFANG,2025,36(24):3091-3095. DOI: 10.6039/j.issn.1001-0408.2025.24.13.
目的
2
分析
HLA-B
*15:02阴性患者发生抗癫痫药物(AEDs)相关严重皮肤不良反应(SCARs)的非遗传风险因素,为临床精准用药提供依据。
方法
2
采用回顾性病例对照设计,纳入2022年1月至2024年12月在我院行
HLA-B
*15:02检测的患者,将患者分为SCARs组(
HLA-B
*15:02阴性且被诊断为SCARs,15例)和对照组(
HLA-B
*15:02阴性的AEDs使用者,38例)。通过单因素分析与多因素Firth惩罚似然逻辑回归模型(Firth回归)评估风险因素,并采用Benjamini-Hochberg错误发现率(FDR)和Firth回归进行校正,采用敏感性分析以量化对照组中卡马西平暴露率可能存在的偏倚对结果的影响。
结果
2
单因素分析结果显示,年龄≥50岁、服用卡马西平、联合使用抗生素/抗病毒药物为发生AEDs相关SCARs的危险因素(OR分别为18.15、7.54、13.46,95%CI分别为4.13~79.84、1.89~30.08、1.36~133.18,均
P
<0.05),服用拉莫三嗪为保护因素[OR为0.10,95%CI为0.02~0.39,
P
<0.05)。经FDR校正后,上述因素仍保持统计学显著性(
P
<0.05)。多因素分析结果显示,年龄≥50岁(校正后OR为16.27,95%CI为3.98~66.55,
P
<0.001)和服用卡马西平(校正后OR为7.11,95%CI为1.82~27.85,
P
=0.005)均是发生AEDs相关SCARs的独立危险因素。敏感性分析结果显示,校正后服用卡马西平的风险OR范围在14.2~28.4之间。
结论
2
在
HLA-B
*15:02阴性患者中,年龄≥50岁和服用卡马西平是发生AEDs相关SCARs的独立非遗传风险因素。建议高龄患者优先选用卡马西平以外的AEDs。
OBJECTIVE
2
To analyze the non-genetic risk factors for severe cutaneous adverse reactions (SCARs) related to antiepileptic drugs (AED
s) in
HLA-B
*15:02 negative patients, and provide a basis for clinical precision medication.
METHODS
2
A retrospective case-control design was used to include patients who underwent
HLA-B
*15:02 testing at our hospital from January 2022 to December 2024. Patients were divided into SCARs group (15 cases who were
HLA-B
*15:02 negative and diagnosed with SCARs) and control group (38 cases who were
HLA-B
*15:02 negative and used AEDs). Risk factors were evaluated using univariate analysis and a multivariable Firth penalty likelihood logistic regression model (Firth regression), and Benjamin-Hochberg false discovery rate (FDR) and Firth regression were used for correction, and sensitivity analysis was used to quantify the impact of potential biases in carbamazepine exposure rates in the control group on the results.
RESULTS
2
Univariate analysis showed that age≥50 years, use of carbamazepine, and combination use of antibiotics/antiviral drugs were risk factors for developing AEDs-related SCARs (OR=18.15, 7.54, 13.46, 95%CI of 4.13-79.84, 1.89-30.08, 1.36-133.18, all
P
<0.05), while taking lamotrigine was a protective factor [OR=0.10, 95%CI of 0.02-0.39,
P
<0.05
]
. After FDR correction, the above factors still maintained statistical significance (
P
<0.05). The results of multivariate analysis showed that age≥50 years [adjusted OR=16.27, 95%CI of 3.98-66.55,
P
<0.001
]
and taking carbamazepine [adjusted OR=7.11, 95%CI of 1.82-27.85,
P
=0.005
]
were independent risk factors for the occurrence of SCARs-related AEDs. The results of sensitivity analysis showed that the adjusted risk OR range for taking carbamazepine was between 14.2 and 28.4.
CONCLUSIONS
2
Age≥50 years and use of carbamazepine are independent non-genetic risk factors for the development of SCARs-related AEDs in
HLA-B
*15:02 negative patients. It is recommended that elderly patients should prioritize the use of AEDs other than carbamazepine.
HUNG S I , MOCKENHAUPT M , BLUMENTHAL K G , et al . Severe cutaneous adverse reactions [J ] . Nat Rev Dis Primers , 2024 , 10 ( 1 ): 30 .
DENG M , SU Y W , WU R F , et al . Clinical features and prognostic factors of severe cutaneous adverse drug reactions:a single-center retrospective study of 209 cases in China [J ] . Int Immunopharmacol , 2023 , 114 : 109530 .
STEWART T J , CHAN C J , SHAH H , et al . Infectious complications of Stevens-Johnson syndrome and toxic epidermal necrolysis:a systematic review and meta-analysis [J ] . Int J Dermatol , 2025 , 64 ( 5 ): 830 - 848 .
GIBSON A , RAM R , GANGULA R , et al . Multiomic single-cell sequencing defines tissue-specific responses in Stevens-Johnson syndrome and toxic epidermal necrolysis [J ] . Nat Commun , 2024 , 15 ( 1 ): 8722 .
PHUNG T H , CONG DUONG K N , JUNIO GLORIA M A , et al . The association between HLA-B*15:02 and phenytoin-induced severe cutaneous adverse reactions:a meta-analysis [J ] . Pharmacogenomics , 2022 , 23 ( 1 ): 49 - 59 .
陈晨 , 江祎 , 师少军 , 等 . 奥卡西平致Stevens-Johnson综合征和中毒性表皮坏死松解症的特点及基因相关性分析 [J ] . 中国药房 , 2017 , 28 ( 5 ): 620 - 625 .
THAM K M , YEK J J L , LIU C W Y . Unraveling the genetic link:an umbrella review on HLA-B*15:02 and antiepileptic drug-induced Stevens-Johnson syndrome/toxic epidermal necrolysis [J ] . Pharmacogenet Genomics , 2024 , 34 ( 5 ): 154 - 165 .
CHANG B L , LIU J R , CHANG S H , et al . Impact on carbamazepine usage and cutaneous adverse reactions before and after the reimbursement of HLA-B*15:02 genotyping in Taiwan,2000-2017:a nationwide longitudinal study [J ] . Epilepsia , 2023 , 64 ( 10 ): 2679 - 2689 .
郭夏青 , 李郭飞 , 孙玉华 , 等 . 拉考沙胺与卡马西平治疗成人新诊癫痫的有效性和安全性对比 [J ] . 中国药房 , 2024 , 35 ( 4 ): 464 - 467 .
SUNG C , TAN L , LIMENTA M , et al . Usage pattern of carbamazepine and associated severe cutaneous adverse reactions in Singapore following implementation of HLA-B*15:02 genotyping as standard-of-care [J ] . Front Pharmacol , 2020 , 11 : 527 .
MANSON L E N , NIJENHUIS M , SOREE B , et al . Dutch Pharmacogenetics Working Group (DPWG) guideline for the gene-drug interaction of CYP2C9 HLA-A and HLA-B with anti-epileptic drugs [J ] . Eur J Hum Genet , 2024 , 32 ( 8 ): 903 - 911 .
李丽娜 , 张俊俊 , 张守民 . 卡马西平致中毒性表皮坏死松解症伴HLA-A*31:01阳性一例 [J ] . 中华皮肤科杂志 , 2020 , 53 ( 11 ): 917 - 919 .
WONG C S M , YAP D Y H , IP P , et al . HLA-B*15:11 status and carbamazepine-induced severe cutaneous adverse drug reactions in HLA-B*15:02 negative Chinese [J ] . Int J Dermatol , 2022 , 61 ( 2 ): 184 - 190 .
AHMED A F , SUKASEM C , SABBAH M A , et al . Genetic determinants in HLA and cytochrome P450 genes in the risk of aromatic antiepileptic-induced severe cuta-neous adverse reactions [J ] . J Pers Med , 2021 , 11 ( 5 ): 383 .
阮旭 , 韩晶晶 , 李宇 , 等 . 卡马西平致HLA-B*1502基因阴性成年患者发生Stevens-Johnson综合征1例并文献分析 [J ] . 中南药学 , 2025 , 23 ( 8 ): 2467 - 2470 .
KOWALSKA J , WRZEŚNIOK D . Skin-related adverse reactions induced by oral antidiabetic drugs:a review of literature and case reports [J ] . Pharmaceuticals(Basel) , 2024 , 17 ( 7 ): 847 .
MANGONI A A , WOODMAN R J , JARMUZEWSKA E A . Pharmacokinetic and pharmacodynamic alterations in older people:what we know so far [J ] . Expert Opin Drug Metab Toxicol , 2025 , 21 ( 7 ): 811 - 829 .
ZGOLLI F , AOUINTI I , CHARFI O , et al . Cutaneous adverse effects of antiepileptic drugs [J ] . Therapie , 2024 , 79 ( 4 ): 453 - 459 .
PAN R Y , CHU M T , WANG C W , et al . Identification of drug-specific public TCR driving severe cutaneous adverse reactions [J ] . Nat Commun , 2019 , 10 ( 1 ): 3569 .
ZHANG C , QIAO P , ZHANG J Y , et al . A carbamazepine metabolite activates NLRP3 and controls skin homing of CD8 + T-cells in SJS/TEN [J ] . J Dermatol Sci , 2024 , 116 ( 3 ): 80 - 89 .
NAKKAM N , KONYOUNG P , AMORNPINYO W , et al . Genetic variants associated with severe cutaneous adverse drug reactions induced by carbamazepine [J ] . Br J Clin Pharmacol , 2022 , 88 ( 2 ): 773 - 786 .
CHUNG W H , WANG C W , DAO R L . Severe cutaneous adverse drug reactions [J ] . J Dermatol , 2016 , 43 ( 7 ): 758 - 766 .
SHI Y W , MIN F L , ZHOU D , et al . HLA-A*24:02 as a common risk factor for antiepileptic drug-induced cuta-neous adverse reactions [J ] . Neurology , 2017 , 88 ( 23 ): 2183 - 2191 .
MENG Q L , GU H Y , ZHANG Q H , et al . Carbamazepine cutaneous adverse reactions and HLA gene variation in the Chinese population:a systematic review and meta-analysis [J ] . Pharmacogenomics , 2023 , 24 ( 8 ): 459 - 474 .
SU S C , HUNG S I , FAN W L , et al . Severe cutaneous adverse reactions:the pharmacogenomics from research to clinical implementation [J ] . Int J Mol Sci , 2016 , 17 ( 11 ): 1890 .
CHOW J C , HUANG C W , FANG C W , et al . Lamotrigine-induced hypersensitivity syndrome in a Han Chinese patient with the HLA-B 5801 genotype [J ] . Neurol Sci , 2013 , 34 ( 1 ): 117 - 119 .
LI W S , WANG J , LIN H J , et al . HLA-A∗24:02 associa-ted with lamotrigine-induced cutaneous adverse drug reactions:a systematic review and meta-analysis [J ] . Medicine(Baltimore) , 2020 , 99 ( 52 ): e23929 .
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