Mikkelsen Thea Falkenberg, Vera-Rodriguez Maria, Greggains Gareth, Fedorcsák Péter, Hald Kirsten
Department of Gynecology, Oslo University Hospital, Oslo, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
F S Rep. 2023 Nov 14;5(1):72-79. doi: 10.1016/j.xfre.2023.11.006. eCollection 2024 Mar.
To compare ribonucleic acid (RNA) quantity and purity in tissue collected with different endometrial sampling methods to establish the optimal tool for use in endometrial gene expression studies.
Observational study.
University hospital.
Fourteen patients with submucosal leiomyomas.
Unguided biopsies were obtained using a low-pressure suction device before hysteroscopy from 14 patients with submucosal leiomyomas followed by guided biopsy with a resectoscope loop. Fifty-seven samples were collected: 25 obtained using a suction device and 32 with a loop.
Total biopsy weight, RNA purity, and RNA yield for each collection method. After complementary deoxyribonucleic acid synthesis, expression was measured by quantitative polymerase chain reaction in the endometrium overlying and remote from the leiomyoma, as similar expression throughout the cavity was a prerequisite for the use of unguided biopsy method.
The median weight of the samples was significantly larger when obtained with the low-pressure suction device than with the resectoscope loop (153 vs. 20 mg). The RNA yield was similar (suction curette, 1,625 ng/mg; resectoscope loop, 1,779 ng/mg). The A260-to-A280 ratio was satisfactory for 94.7 % of the samples, with no difference between the groups. The endometrial expression of was similar in areas overlying the leiomyoma compared with that in remote endometrial sites (2 = 0.0224 vs. 0.0225).
Low-pressure endometrial suction devices provide tissue samples with acceptable RNA purity and quantity for gene expression studies. The expression of did not differ between endometrial sampling sites even in the presence of leiomyomas.
比较采用不同子宫内膜取样方法所采集组织中的核糖核酸(RNA)数量和纯度,以确定用于子宫内膜基因表达研究的最佳工具。
观察性研究。
大学医院。
14例黏膜下平滑肌瘤患者。
在宫腔镜检查前,使用低压吸引装置对14例黏膜下平滑肌瘤患者进行盲目活检,随后用切除镜环进行引导活检。共采集57个样本:25个通过吸引装置获取,32个通过切除镜环获取。
每种采集方法的活检总重量、RNA纯度和RNA产量。在互补脱氧核糖核酸合成后,通过定量聚合酶链反应测量平滑肌瘤上方及远离平滑肌瘤的子宫内膜中的表达,因为整个宫腔内表达相似是使用盲目活检方法的前提条件。
使用低压吸引装置获取的样本中位数重量显著大于使用切除镜环获取的样本(153 vs. 20 mg)。RNA产量相似(吸引刮匙,1625 ng/mg;切除镜环,1779 ng/mg)。94.7%的样本A260/A280比值令人满意,两组之间无差异。与远离平滑肌瘤的子宫内膜部位相比,平滑肌瘤上方区域的子宫内膜 表达相似(2 = 0.0224 vs. 0.0225)。
低压子宫内膜吸引装置可为基因表达研究提供RNA纯度和数量均可接受的组织样本。即使存在平滑肌瘤,子宫内膜取样部位之间的 表达也无差异。