中国临床新医学
中國臨床新醫學
중국림상신의학
CHINESE JOURNAL OF NEW CLINICAL MEDICINE
2015年
6期
530-533
,共4页
阿德福韦酯%慢性乙型肝炎%应答不佳
阿德福韋酯%慢性乙型肝炎%應答不佳
아덕복위지%만성을형간염%응답불가
Adforvir dipivoxil%Chronic hepatitis B%Poor response
目的:探讨阿德福韦酯治疗初治慢性乙型肝炎( chronic hepatitis B,CHB)过程中应答不佳的相关因素。方法收集2011-01~2014-01应用阿德福韦酯治疗80例CHB患者的临床资料,其中HBeAg阳性患者46例,HBeAg阴性患者34例,分析阿德福韦酯治疗CHB应答不佳的相关因素。结果 HBeAg阳性CHB患者中,治疗前HBV DNA载量、HBsAg定量、体重指数是完全应答与否的影响因素( P<0.05)。 HBeAg阴性CHB患者中,治疗前HBV DNA载量、体重指数是完全应答与否的影响因素( P<0.05)。 HBeAg 阳性时, rtA181V和rtN236T位点变异率≥5%时易引起应答不佳( P<0.05)。 HBeAg阴性时,rtN236T≥5%时易引起应答不佳(P<0.05),rtA181V<5%与应答不佳无关(P>0.05)。 HBeAg阳性组治疗4周时,HBV DNA下降幅度对应答没有明显影响(P>0.05)。治疗12周、24周时,HBV DNA下降幅度在低于(1.326±0.907)log10copies/ml、(1.279±1.156)log10copies/ml时容易出现应答不佳(P<0.05)。 HBeAg阴性组治疗4周时,HBV DNA下降幅度对应答没有明显影响(P>0.05)。治疗12周、24周时,HBV DNA下降幅度在低于(0.983±0.706)log10copies/ml、(1.178±0.736)log10copies/ml时容易出现应答不佳(P<0.05)。而未发现谷丙转氨酶(ALT)、谷草转氨酶(AST)的变化幅度对应答有影响(P>0.05)。结论患者的基线资料及治疗过程中HBV DNA下降幅度是阿德福韦酯治疗CHB出现应答不佳的影响因素,应根据患者的基本情况制定个体化的治疗方案,以降低应答不佳现象的发生率。
目的:探討阿德福韋酯治療初治慢性乙型肝炎( chronic hepatitis B,CHB)過程中應答不佳的相關因素。方法收集2011-01~2014-01應用阿德福韋酯治療80例CHB患者的臨床資料,其中HBeAg暘性患者46例,HBeAg陰性患者34例,分析阿德福韋酯治療CHB應答不佳的相關因素。結果 HBeAg暘性CHB患者中,治療前HBV DNA載量、HBsAg定量、體重指數是完全應答與否的影響因素( P<0.05)。 HBeAg陰性CHB患者中,治療前HBV DNA載量、體重指數是完全應答與否的影響因素( P<0.05)。 HBeAg 暘性時, rtA181V和rtN236T位點變異率≥5%時易引起應答不佳( P<0.05)。 HBeAg陰性時,rtN236T≥5%時易引起應答不佳(P<0.05),rtA181V<5%與應答不佳無關(P>0.05)。 HBeAg暘性組治療4週時,HBV DNA下降幅度對應答沒有明顯影響(P>0.05)。治療12週、24週時,HBV DNA下降幅度在低于(1.326±0.907)log10copies/ml、(1.279±1.156)log10copies/ml時容易齣現應答不佳(P<0.05)。 HBeAg陰性組治療4週時,HBV DNA下降幅度對應答沒有明顯影響(P>0.05)。治療12週、24週時,HBV DNA下降幅度在低于(0.983±0.706)log10copies/ml、(1.178±0.736)log10copies/ml時容易齣現應答不佳(P<0.05)。而未髮現穀丙轉氨酶(ALT)、穀草轉氨酶(AST)的變化幅度對應答有影響(P>0.05)。結論患者的基線資料及治療過程中HBV DNA下降幅度是阿德福韋酯治療CHB齣現應答不佳的影響因素,應根據患者的基本情況製定箇體化的治療方案,以降低應答不佳現象的髮生率。
목적:탐토아덕복위지치료초치만성을형간염( chronic hepatitis B,CHB)과정중응답불가적상관인소。방법수집2011-01~2014-01응용아덕복위지치료80례CHB환자적림상자료,기중HBeAg양성환자46례,HBeAg음성환자34례,분석아덕복위지치료CHB응답불가적상관인소。결과 HBeAg양성CHB환자중,치료전HBV DNA재량、HBsAg정량、체중지수시완전응답여부적영향인소( P<0.05)。 HBeAg음성CHB환자중,치료전HBV DNA재량、체중지수시완전응답여부적영향인소( P<0.05)。 HBeAg 양성시, rtA181V화rtN236T위점변이솔≥5%시역인기응답불가( P<0.05)。 HBeAg음성시,rtN236T≥5%시역인기응답불가(P<0.05),rtA181V<5%여응답불가무관(P>0.05)。 HBeAg양성조치료4주시,HBV DNA하강폭도대응답몰유명현영향(P>0.05)。치료12주、24주시,HBV DNA하강폭도재저우(1.326±0.907)log10copies/ml、(1.279±1.156)log10copies/ml시용역출현응답불가(P<0.05)。 HBeAg음성조치료4주시,HBV DNA하강폭도대응답몰유명현영향(P>0.05)。치료12주、24주시,HBV DNA하강폭도재저우(0.983±0.706)log10copies/ml、(1.178±0.736)log10copies/ml시용역출현응답불가(P<0.05)。이미발현곡병전안매(ALT)、곡초전안매(AST)적변화폭도대응답유영향(P>0.05)。결론환자적기선자료급치료과정중HBV DNA하강폭도시아덕복위지치료CHB출현응답불가적영향인소,응근거환자적기본정황제정개체화적치료방안,이강저응답불가현상적발생솔。
Objective To investigate the factors of poor virological response to adforvir dipivoxil(ADV) treatment in patients with chronic hepatitis B.Methods The clinical data of the factors of poor virological response to ADV treatment in patients with chronic hepatitis B were retrospectively analyzed from January 2011 to January 2014. Results BMI, HBV DNA, HBsAg when HBeAg was positive and BMI, HBV DNA when HBeAg was negative were correlated with the response(P<0.05).There was significantly difference in V of 181 mutations (≥5%) and T of 236 mutations (≥5%) when HBeAg was positive ( P<0.05) .There was significantly difference in T of 236 muta-tions (≥5%) when HBeAg was negative(P<0.05).But there were no significant differences in V of 181 mutations (<5%) when HBeAg was negative ( P>0.05 ) .HBV DNA which was lower than the basic levels in 12 and 24 weeks after treatment (1.326 ±0.907)log10copies/ml and (1.279 ±1.156)log10copies/ml was easy to have the poor virological response(P<0.05) in the HBeAg positive patients.HBV DNA which was lower than the basic levels in 12 and 24 weeks after treatment (0.983 ±0.706) log10copies/ml and (1.178 ±0.736) log10copies/ml was easy to have the poor virological response( P<0.05) in the HBeAg negative patients.There were no obvious relationships between the changes of ALT and AST and the response(P>0.05).Conclusion The baseline data and the changes of HBV DNA are the factors of poor virological response to ADV treatment in patients with chronic hepatitis B.Individual-ized treatments should be established according to the above data to reduce the incidence of poor response phenomenon.