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标题: 兒童慢性乙型肝炎HBsAg血清學轉換的預測 [打印本页]

作者: StephenW    时间: 2021-12-6 17:24     标题: 兒童慢性乙型肝炎HBsAg血清學轉換的預測

兒童慢性乙型肝炎HBsAg血清學轉換的預測
鍾燕偉#1、施燕敏#2、方楚#2、劉潔3、策實2、徐嬌嬌2 3、劉鵬2、白燕潔4、肖和5、張秀昌 6 , 張敏 7
隸屬關係
隸屬關係

    1
    中國人民解放軍總醫院第五醫學中心肝病科,北京西四環中路100號,100039。 [email protected]
    2
    中國人民解放軍總醫院第五醫學中心肝病科,北京西四環中路100號,100039。
    3
    中國河北省張家口省高新區鑽石南路11號河北北方大學,075000。
    4
    北京大學第三醫院,北京花園北路 49 號,中國 100191。
    5
    中國人民解放軍總醫院第五醫學中心肝病科,北京西四環中路100號,100039。 [email protected]
    6
    中國河北省張家口省高新區鑽石南路11號河北北方大學,075000。 [email protected]
    7
    中國人民解放軍總醫院第五醫學中心肝病科,北京西四環中路100號,100039。張敏[email protected]

#
同等貢獻。

    PMID:34863101 DOI:10.1186/s12879-021-06883-1

抽象的

背景:建立兒童慢性乙型肝炎(CHB)HBsAg血清學轉換的預測,以幫助臨床醫生選擇治療策略。

方法:選取解放軍總醫院第五醫學中心收治的1~17歲HBeAg陽性CHB患兒63例,接受干擾素α(IFNα)治療48週,並測量臨床資料。根據第48週HBsAg血清學轉換(HBsAg < 0.05 IU/mL和抗-HBsAg > 10 IU/L)結果,將患者分為HBsAg血清學轉換(S)組和非HBsAg血清學轉換(NS)組。多變量 COX 回歸用於確定與 HBsAg 血清學轉換相關的影響因素。建立了一種新的預測指數,並使用受試者工作特徵曲線下面積 (AUROC) 來評估對 HBsAg 血清學轉換的預測。

結果:63例患者分為S組(20.6%,13/63)和NS組(79.4%,50/63)。單變量和多變量分析確定年齡、基線肝內 cccDNA 和血清 HBsAg 水平是 HBsAg 血清學轉換的獨立影響因素。肝內 cccDNA 與血清 HBsAg 呈正相關(r = 0.464,p = 0.000)。 HBV cccDNA 的 AUROC 為 0.83(95% CI 0.71 至 0.95),基線 HBsAg 的 AUROC 為 0.77(95% CI 0.61 至 0.92)。以肝內cccDNA≤0.08 log10拷貝/106個細胞為臨界值,HBsAg血清轉換的陽性預測值(PPV)和陰性預測值(NPV)分別為86.8%和60.0%,敏感性為92.0%,特異性為56.2%。 HBsAg ≤ 3.68 log10 IU/mL 作為截斷值,HBsAg 血清學轉換的 PPV 和 NPV 分別為 91.2% 和 56.3%;敏感性和特異性分別為 69.2% 和 86.0%。它們之間在預測 HBsAg 血清學轉換方面沒有統計學差異(p = 0.146)。

結論: HBsAg 血清學轉換可通過基線血清 HBsAg 或肝內 cccDNA 預測 CHB 兒童。利用該指標,臨床醫生可以選擇更合理的治療策略,減少醫療資源的浪費。

關鍵詞:兒童;慢性乙型肝炎; HBV cccDNA;乙肝表面抗原; HBsAg 血清學轉換。
作者: StephenW    时间: 2021-12-6 17:24

Prediction for HBsAg seroconversion in children with chronic hepatitis B
Yan-Wei Zhong #  1 , Yan-Min Shi #  2 , Fang Chu #  2 , Jie Liu  3 , Ce Shi  2 , Jiao-Jiao Xu  2   3 , Peng Liu  2 , Yan-Jie Bai  4 , Xiao-He Xiao  5 , Xiu-Chang Zhang  6 , Min Zhang  7
Affiliations
Affiliations

    1
    Senior Department of Hepatology, the Fifth Medical Center of Chinese PLA General Hospital, Xisihuan Mid-Road No.100, 100039, Beijing, China. [email protected].
    2
    Senior Department of Hepatology, the Fifth Medical Center of Chinese PLA General Hospital, Xisihuan Mid-Road No.100, 100039, Beijing, China.
    3
    Hebei North University, South Diamond Road No.11, High Tech Zone, Zhangjiakou Province, 075000, Hebei, China.
    4
    Peking University Third Hospital, 49 North Garden Rd., Beijing, 100191, China.
    5
    Senior Department of Hepatology, the Fifth Medical Center of Chinese PLA General Hospital, Xisihuan Mid-Road No.100, 100039, Beijing, China. [email protected].
    6
    Hebei North University, South Diamond Road No.11, High Tech Zone, Zhangjiakou Province, 075000, Hebei, China. [email protected].
    7
    Senior Department of Hepatology, the Fifth Medical Center of Chinese PLA General Hospital, Xisihuan Mid-Road No.100, 100039, Beijing, China. [email protected].

#
Contributed equally.

    PMID: 34863101 DOI: 10.1186/s12879-021-06883-1

Abstract

Background: To establish a prediction of HBsAg seroconversion in children with chronic hepatitis B (CHB), so as to help clinicians to choose therapeutic strategy.

Methods: A total of 63 children with HBeAg-positive CHB aged 1 to 17 years, who admitted to the fifth medical center of Chinese PLA general hospital and treated with interferon α (IFNα) 48 weeks were enrolled, the clinical data were measured. Based on the results of HBsAg seroconversion (HBsAg < 0.05 IU/mL and anti-HBsAg > 10 IU/L) at week 48, the patients were divided into HBsAg seroconversion (S) group and non-HBsAg seroconversion (NS) group. Multivariate COX regression was used to identify the impact factors associated with HBsAg seroconversion. A novel prediction index was established and the area under the receiver operating characteristic curve (AUROC) was used to assess the prediction for HBsAg seroconversion.

Results: The 63 patients were divided into S group (20.6%, 13/63) and NS group (79.4%, 50/63). Univariate and multivariate analysis identified age, baseline intrahepatic cccDNA and serum HBsAg levels were independent impact factors for HBsAg seroconversion. Intrahepatic cccDNA was positively correlated with serum HBsAg (r = 0.464, p = 0.000). AUROC of HBV cccDNA was 0.83 (95% CI 0.71 to 0.95) and AUROC of baseline HBsAg was 0.77 (95% CI 0.61 to 0.92). Intrahepatic cccDNA ≤ 0.08 log10 copies/106 cell is regarded as cutoff value, the positive predictive value(PPV) and negative predictive value(NPV) for HBsAg seroconversion were 86.8% and 60.0%, respectively, with a sensitivity of 92.0% and specificity of 56.2%. HBsAg ≤ 3.68 log10 IU/mL is used as cut off value, the PPV and NPV for HBsAg seroconversion were 91.2% and 56.3%, respectively; the sensitivity and specificity was 86.0% of 69.2%, respectively. There was no statistical difference between them for predicting HBsAg seroconversion (p = 0.146).

Conclusions: HBsAg seroconversion can be predicted by the baseline serum HBsAg or intrahepatic cccDNA in children with CHB. Using the index, clinicians can choose more reasonable therapeutic strategy and reduce the waste of medical resources.

Keywords: Children; Chronic hepatitis B; HBV cccDNA; HBsAg; HBsAg seroconversion.
作者: StephenW    时间: 2021-12-6 17:25

https://bmcinfectdis.biomedcentr ... 879-021-06883-1.pdf




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