Lin Wayne, Titus Shiny, Moy Fred, Ginsburg Elizabeth S, Oktay Kutluk
Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115.
Laboratory of Molecular Reproduction and Fertility Preservation, Department of Obstetrics and Gynecology, Yale University School of Medicine, New Haven, Connecticut 06510.
J Clin Endocrinol Metab. 2017 Oct 1;102(10):3839-3847. doi: 10.1210/jc.2017-00765.
Recent clinical and laboratory studies suggested that women with BRCA mutations have lower ovarian reserve and their primordial follicle oocytes may be more prone to DNA damage; however, direct proof is lacking.
To determine whether women with germline BRCA mutations have reduced primordial follicle reserve and increased oocyte DNA damage.
A comparative laboratory study of ovarian tissue obtained from unaffected BRCA mutation carriers (BMCs) vs age-matched organ donor cadavers.
Two academic centers.
Of the 230 ovarian specimens from BMCs, 18 met the study inclusion criteria. Healthy ovaries from 12 organ donor cadavers served as controls.
Histology and immunohistochemical analysis on paraffin-embedded ovarian sections.
MAIN OUTCOME MEASURE(S): Primordial follicle density and the percentage of DNA double-strand break (DSB)-positive primordial follicle oocytes.
Ovaries from BMCs had significantly lower primordial follicle densities than those of controls (11.2 ± 2.0 vs 44.2 ± 6.2 follicles/mm3; P = 0.0002). BRCA mutations were associated with increased DNA DSBs in primordial follicle oocytes (62% ± 5.2% vs 36% ± 3.4%; P = 0.0005). In subgroup analyses, both BRCA1 and BRCA2 mutations were associated with lower primordial follicle density (P = 0.0001 and 0.0030, respectively), and BRCA1 mutations were associated with higher DNA DSBs (P = 0.0003) than controls. The rates of follicle decline (R2 = 0.74; P = 0.0001) and DNA DSB accumulation (R2 = 0.70; P = 0.0001) appeared to be accelerated, particularly in primordial follicle oocytes of BMCs over age 30 years.
We provide direct evidence of diminished ovarian reserve as well as accelerated primordial follicle loss and oocyte DNA damage in women with BRCA mutations. These findings may further our understanding of ovarian aging, and be useful when counseling BMCs.
近期的临床和实验室研究表明,携带BRCA突变的女性卵巢储备较低,其原始卵泡卵母细胞可能更容易发生DNA损伤;然而,缺乏直接证据。
确定携带种系BRCA突变的女性是否原始卵泡储备减少以及卵母细胞DNA损伤增加。
一项对未受影响的BRCA突变携带者(BMC)与年龄匹配的器官捐赠者尸体的卵巢组织进行的对比实验室研究。
两个学术中心。
在230份来自BMC的卵巢标本中,18份符合研究纳入标准。来自12名器官捐赠者尸体的健康卵巢作为对照。
对石蜡包埋的卵巢切片进行组织学和免疫组织化学分析。
原始卵泡密度和DNA双链断裂(DSB)阳性原始卵泡卵母细胞的百分比。
BMC的卵巢原始卵泡密度显著低于对照组(11.2±2.0个/立方毫米对44.2±6.2个/立方毫米;P = 0.0002)。BRCA突变与原始卵泡卵母细胞中DNA DSB增加相关(62%±5.2%对36%±3.4%;P = 0.0005)。在亚组分析中,BRCA1和BRCA2突变均与较低的原始卵泡密度相关(分别为P = 0.0001和0.0030),且BRCA1突变与比对照组更高的DNA DSB相关(P = 0.0003)。卵泡减少率(R2 = 0.74;P = 0.0001)和DNA DSB积累率(R2 = 0.70;P = 0.0001)似乎加速,特别是在30岁以上BMC的原始卵泡卵母细胞中。
我们提供了直接证据,证明携带BRCA突变的女性卵巢储备减少,以及原始卵泡加速丢失和卵母细胞DNA损伤。这些发现可能会增进我们对卵巢衰老的理解,并在为BMC提供咨询时有用。