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The influence of probiotics on genital high-risk human papilloma virus clearance and quality of cervical smear: a randomized placebo-controlled trial
BMC Women's Health Pub Date : 2019-07-24 , DOI: 10.1186/s12905-019-0798-y
Yu-Che Ou , Hung-Chun Fu , Chih-Wen Tseng , Chen-Hsuan Wu , Ching-Chou Tsai , Hao Lin

Probiotics has been shown to be effective in reducing vaginal colonization of pathogenic organisms. The aim of this study was to investigate the influence of probiotic strains Lactobacillus rhamnosus GR-1 and Lactobacillus reuteri RC-14 on genital high-risk human papilloma virus (HR-HPV) clearance and quality of cervical smear. This was a randomized, double-blinded, placebo-controlled trial. Women with genital HR-HPV infection were randomized into study and control groups. A probiotic or placebo preparation was administered orally (one capsule daily) until negative HR-HPV testing. A cervical smear and HR-HPV tests were performed at the beginning of the study and every 3 months thereafter until a negative result was obtained. A total of 121 women with genital HR-HPV infection were enrolled (62 in the study group and 59 in the control group). There was no significant difference in HR-HPV clearance rate between the two groups (58.1% vs. 54.2%). The only factor predicting HR-HPV clearance was a lower initial viral load (HR 3.214; 95% CI: 1.398, 7.392; p = 0.006). Twenty-two women had a mildly abnormal initial cervical smear and nine had an unsatisfactory smear. At 6 months follow-up, both mildly abnormal cervical smear and unsatisfactory smear rates had decreased significantly in the study group compared to the control group (p = 0.017 and 0.027). The application of probiotic strains Lactobacillus rhamnosus GR-1 and Lactobacillus reuteri RC-14 did not influence genital HR-HPV clearance, but may have decreased the rates of mildly abnormal and unsatisfactory cervical smears. Clinicaltrials.gov NCT01599416 , May, 2012. Retrospectively registered.

中文翻译:

益生菌对生殖器高危型人乳头瘤病毒清除率和宫颈涂片质量的影响:一项随机安慰剂对照试验

益生菌已显示可有效减少病原生物在阴道中的定植。这项研究的目的是调查益生菌菌株鼠李糖乳杆菌GR-1和罗伊氏乳杆菌RC-14对生殖器高危型人乳头瘤病毒(HR-HPV)清除率和宫颈涂片质量的影响。这是一项随机,双盲,安慰剂对照试验。生殖器HR-HPV感染的妇女被随机分为研究组和对照组。口服(每天一粒胶囊)益生菌或安慰剂制剂,直到HR-HPV检测阴性。在研究开始时进行宫颈涂片和HR-HPV检测,此后每3个月进行一次,直至获得阴性结果。共有121名患有生殖器HR-HPV感染的女性入组(研究组62例,对照组59例)。两组之间的HR-HPV清除率无显着差异(58.1%对54.2%)。预测HR-HPV清除率的唯一因素是较低的初始病毒载量(HR 3.214; 95%CI:1.398,7.392; p = 0.006)。22名女性最初的子宫颈涂片有轻度异常,而9名女性的涂片不令人满意。随访6个月,与对照组相比,研究组的轻度异常宫颈涂片和不满意的涂片率均显着降低(p = 0.017和0.027)。益生菌菌株鼠李糖乳杆菌GR-1和罗伊氏乳杆菌RC-14的使用不影响生殖器HR-HPV清除率,但可能降低了轻度异常和不满意的宫颈涂片的发生率。Clinicaltrials.gov NCT01599416,2012年5月。
更新日期:2019-07-24
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