Associations between improvement in genitourinary symptoms of menopause and changes in the vaginal ecosystem.
Associations between improvement in genitourinary symptoms of menopause and changes in the vaginal ecosystem.
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DOI:
10.1097/gme.0000000000001037
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发表时间:
2018-05
期刊:
影响因子:
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通讯作者:
Fredricks DN
中科院分区:
文献类型:
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作者:
Mitchell CM;Srinivasan S;Plantinga A;Wu MC;Reed SD;Guthrie KA;LaCroix AZ;Fiedler T;Munch M;Liu C;Hoffman NG;Blair IA;Newton K;Freeman EW;Joffe H;Cohen L;Fredricks DN
Identify associations between improvement in genitourinary symptoms of menopause (GSM) and vaginal microbiota, vaginal glycogen and serum estrogen. Thirty postmenopausal women enrolled in a hot flash treatment trial (oral estradiol vs. venlafaxine vs. placebo) who reported GSM and provided vaginal swabs at 0, 4 and 8 weeks were studied. Bacterial communities were characterized using deep sequencing targeting the 16S rRNA gene V3–V4 region. Participants selected a most bothersome genitourinary symptom (dryness, discharge, pain, itch/burn or inability to have sex) and rated severity on a 10-point scale at baseline and 8 weeks. Vaginal glycogen and serum estradiol and estrone were measured at enrollment and 8 weeks. Comparisons according to improvement in most bothersome symptom (MBS) were made using chi-square, Wilcoxon signed-rank test, or Hotelling’s t test. Of 30 participants, 21 (70%) had improvement in MBS over the 8-week study, and 9 (30%) had no improvement or worsening of MBS. A higher proportion of women receiving estradiol or venlafaxine reported improvement in MBS (88%, 78%) compared to placebo (54%; p = 0.28). MBS improvement was associated with Lactobacillus-dominant vaginal microbiota at enrollment (57% vs 22%, p = 0.08). Vaginal glycogen, serum estradiol and estrone increased significantly in women whose MBS improved. Improvement in GSM was more common in women receiving oral estradiol or venlafaxine and those with Lactobacillus-dominant vaginal microbiota at enrollment but differences were not statistically significant. Larger trials are need to determine whether vaginal microbiota modify or mediate treatment responses in women with GSM.