中华风湿病学杂志
中華風濕病學雜誌
중화풍습병학잡지
CHINESE JOURNAL OF RHEUMATOLOGY
2015年
4期
261-266
,共6页
喻一奇%宣丹旦%王佳俐%邵凌云%张文宏%邹和建
喻一奇%宣丹旦%王佳俐%邵凌雲%張文宏%鄒和建
유일기%선단단%왕가리%소릉운%장문굉%추화건
乙型肝炎病毒%风湿性疾病%糖皮质激素类%抗风湿药%肿瘤坏死因子-α拮抗剂
乙型肝炎病毒%風濕性疾病%糖皮質激素類%抗風濕藥%腫瘤壞死因子-α拮抗劑
을형간염병독%풍습성질병%당피질격소류%항풍습약%종류배사인자-α길항제
Hepatitis B virus%Rheumatic diseases%Glucocorticoids%Antirheumatic agents%Tumor necrosis factor-alpha-blocking agent
目的 观察12例风湿性疾病合并乙型肝炎病毒(HBV)感染患者接受不同免疫抑制剂治疗后对HBV再激活的影响,并评估对不同免疫抑制剂是否均有必要进行预防性抗病毒治疗.方法 对2008年1月至2012年3月确诊风湿性疾病合并HBV感染的12例患者进行长期随访.在随访期间定期检测患者肝功能、血清HBV DNA水平.结果 中位随访时间为41个月(16~48个月).4例患者接受激素治疗,其中2例未接受预防性抗病毒治疗的患者最终出现HBV再激活,经拉米夫定或恩替卡韦抗病毒治疗后,两者的HBV复制均得到控制.5例接受DMARDs治疗和3例接受肿瘤坏死因子拮抗剂(TNFBA)治疗的患者均未接受预防性抗病毒治疗,且在随访中均未出现HBV再激活.结论 风湿性疾病合并HBV感染的患者在接受免疫抑制剂治疗后可出现HBV再激活.对需要接受激素治疗的风湿性疾病患者,推荐在治疗开始前进行预防性抗病毒治疗.而DMARDs和TNFBA对风湿性疾病合并HBV感染患者而言,仍是一种相对安全的免疫抑制剂.尽管DMARDs和TNFBA治疗后引起HBV再激活的风险较低,在治疗过程中仍必须密切监测患者的HBV DNA和肝功能水平.
目的 觀察12例風濕性疾病閤併乙型肝炎病毒(HBV)感染患者接受不同免疫抑製劑治療後對HBV再激活的影響,併評估對不同免疫抑製劑是否均有必要進行預防性抗病毒治療.方法 對2008年1月至2012年3月確診風濕性疾病閤併HBV感染的12例患者進行長期隨訪.在隨訪期間定期檢測患者肝功能、血清HBV DNA水平.結果 中位隨訪時間為41箇月(16~48箇月).4例患者接受激素治療,其中2例未接受預防性抗病毒治療的患者最終齣現HBV再激活,經拉米伕定或恩替卡韋抗病毒治療後,兩者的HBV複製均得到控製.5例接受DMARDs治療和3例接受腫瘤壞死因子拮抗劑(TNFBA)治療的患者均未接受預防性抗病毒治療,且在隨訪中均未齣現HBV再激活.結論 風濕性疾病閤併HBV感染的患者在接受免疫抑製劑治療後可齣現HBV再激活.對需要接受激素治療的風濕性疾病患者,推薦在治療開始前進行預防性抗病毒治療.而DMARDs和TNFBA對風濕性疾病閤併HBV感染患者而言,仍是一種相對安全的免疫抑製劑.儘管DMARDs和TNFBA治療後引起HBV再激活的風險較低,在治療過程中仍必鬚密切鑑測患者的HBV DNA和肝功能水平.
목적 관찰12례풍습성질병합병을형간염병독(HBV)감염환자접수불동면역억제제치료후대HBV재격활적영향,병평고대불동면역억제제시부균유필요진행예방성항병독치료.방법 대2008년1월지2012년3월학진풍습성질병합병HBV감염적12례환자진행장기수방.재수방기간정기검측환자간공능、혈청HBV DNA수평.결과 중위수방시간위41개월(16~48개월).4례환자접수격소치료,기중2례미접수예방성항병독치료적환자최종출현HBV재격활,경랍미부정혹은체잡위항병독치료후,량자적HBV복제균득도공제.5례접수DMARDs치료화3례접수종류배사인자길항제(TNFBA)치료적환자균미접수예방성항병독치료,차재수방중균미출현HBV재격활.결론 풍습성질병합병HBV감염적환자재접수면역억제제치료후가출현HBV재격활.대수요접수격소치료적풍습성질병환자,추천재치료개시전진행예방성항병독치료.이DMARDs화TNFBA대풍습성질병합병HBV감염환자이언,잉시일충상대안전적면역억제제.진관DMARDs화TNFBA치료후인기HBV재격활적풍험교저,재치료과정중잉필수밀절감측환자적HBV DNA화간공능수평.
Objective To observe hepatitis B virus (HBV) reactivation in 12 patients with rheumatic disease undergoing immunosuppressive therapy and to evaluate whether preemptive antiviral therapy is necessary for patients receiving disease-modifying anti-rheumatic drugs (DMARDs).Methods From January 2008 to March 2012,a total of 12 HBV-infected patients with rheumatic diseases were consecutively enrolled into this long-term follow-up study.Liver function and serum levels of HBV DNA were tested during the follow-up.Results The medium duration of follow-up was 41 months (range 16-48).Four patients received steroid treatment,and among them two patients without pre-emptive antiviral therapy developed HBV reactivation.After administr-ation of LAM or ETV,HBV replication was controlled in both patients.Five patients were treated with disease-modifying anti-rheumatic drugs and the other three patients received tumor necrosis factor-alpha-blocking agents.None of these patients received pre-emptive antiviral therapy.HBV reactivation did not occur in any of them.Conclusion HBV reactivation does occur in HBV-infected patients with rheumatoid diseases after immunosuppressive therapy.Pre-emptive antiviral therapy should be administered in patients who are receiving steroid therapy for rheumatic diseases.In contrast,DMARDs and TNFBA are relatively safe for HBV-infected patients with rheumatic diseases.Close monitoring of HBV DNA and ALT levels is necessary to the mana-gement of HBV reactivation.