Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, University of Utah School of Medicine, Salt Lake City, UT, USA.
Intermountain Healthcare, Murray, UT, USA.
Hum Reprod. 2023 Oct 3;38(10):1991-1997. doi: 10.1093/humrep/dead168.
How does the number of children in women with primary ovarian insufficiency (POI) compare to the number for control women across their reproductive lifespans?
Approximately 14% fewer women with POI will have children, but for those able to have children the median number is 1 less than for age-matched controls.
Women with POI are often identified when presenting for fertility treatment, but some women with POI already have children and there remains a low chance for pregnancy after the diagnosis. Further, POI is heritable, but it is not known whether relatives of women with POI have a smaller family size than relatives of controls.
STUDY DESIGN, SIZE, DURATION: The study was a retrospective case-control study of women with POI diagnosed from 1995 to 2021 (n = 393) and age-matched controls (n = 393).
PARTICIPANTS/MATERIALS, SETTING, METHODS: Women with POI were identified using ICD9 and 10 codes in electronic medical records (1995-2021) from two major healthcare systems in Utah and reviewed for accuracy. Cases were linked to genealogy information in the Utah Population Database. All POI cases (n = 393) were required to have genealogy information available for at least three generations of ancestors. Two sets of female controls were identified: one matched for birthplace (Utah or elsewhere) and 5-year birth cohort, and a second also matched for fertility status (children present). The number of children born and maternal age at each birth were ascertained by birth certificates (available from 1915 to 2020) for probands, controls, and their relatives. The Mann-Whitney U test was used for comparisons. A subset analysis was performed on women with POI and controls who delivered at least one child and on women who reached 45 years to capture reproductive lifespan.
Of the 393 women with POI and controls, 211 women with POI (53.7%), and 266 controls (67.7%) had at least one child. There were fewer children born to women with POI versus controls (median (interquartile range) 1 (0-2) versus 2 (0-3); P = 3.33 × 10-6). There were no children born to women with POI and primary amenorrhea or those <25 years old before their diagnosis. When analyzing women with at least one child, women with POI had fewer children compared to controls overall (2 (1-3) versus 2 (2-4); P = 0.017) and when analyzing women who reached 45 years old (2 (1-3) versus 3 (2-4); P = 0.0073). Excluding known donor oocyte pregnancies, 7.1% of women with POI had children born after their diagnosis. There were no differences in the number of children born to relatives of women with POI, including those with familial POI.
LIMITATIONS, REASONS FOR CAUTION: The data are limited based on inability to determine whether women were trying for pregnancy throughout their reproductive lifespan or were using contraception. Unassisted births after the diagnosis of POI may be slightly over-estimated based on incomplete data regarding use of donor oocytes. The results may not be generalizable to countries or states with late first births or lower birth rates.
Approximately half of women with POI will bear children before diagnosis. Although women with POI had fewer children than age matched controls, the difference in number of children is one child per woman. The data suggest that fertility may not be compromised leading up to the diagnosis of POI for women diagnosed at 25 years or later and with secondary amenorrhea. However, the rate of pregnancy after the diagnosis is low and we confirm a birth rate of <10%. The smaller number of children did not extend to relatives when examined as a group, suggesting that it may be difficult to predict POI based on family history.
STUDY FUNDING/COMPETING INTEREST(S): The work in this publication was supported by R56HD090159 and R01HD099487 (C.K.W.). We also acknowledge partial support for the Utah Population Database through grant P30 CA2014 from the National Cancer Institute. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The authors have no conflicts of interest.
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原发性卵巢功能不全 (POI) 女性的子女数量与同龄对照女性在整个生育期的子女数量相比如何?
患有 POI 的女性生育子女的数量平均比对照组少 14%,但对于能够生育子女的女性,中位数比年龄匹配的对照组少 1 个。
患有 POI 的女性通常在接受生育治疗时被诊断出来,但有些患有 POI 的女性已经有了孩子,而且在诊断后怀孕的机会仍然很低。此外,POI 是遗传性的,但尚不清楚患有 POI 的女性的亲属是否比对照组的亲属家庭规模更小。
研究设计、规模、持续时间:这是一项回顾性病例对照研究,纳入了 1995 年至 2021 年间诊断为 POI 的女性(n=393)和年龄匹配的对照组女性(n=393)。
参与者/材料、设置、方法:通过犹他州两个主要医疗保健系统中的电子病历(1995-2021 年)使用 ICD9 和 10 代码识别 POI 病例,并对其准确性进行审查。病例与犹他州人口数据库中的家谱信息相关联。所有 POI 病例(n=393)均要求至少有三代以上的祖先家谱信息可用。确定了两组女性对照:一组按出生地(犹他州或其他地方)和 5 年出生队列匹配,另一组也按生育状况(有孩子)匹配。通过出生证明(1915 年至 2020 年可用)确定先证者、对照者及其亲属的出生子女数量和母亲生育时的年龄。采用 Mann-Whitney U 检验进行比较。对至少生育过一个孩子的 POI 女性和对照组女性以及达到 45 岁的女性进行了亚组分析,以捕获生育寿命。
在 393 名 POI 女性和对照组中,211 名 POI 女性(53.7%)和 266 名对照组(67.7%)至少有一个孩子。与对照组相比,POI 女性生育的子女数量较少(中位数(四分位距)1(0-2)与 2(0-3);P=3.33×10-6)。POI 女性原发性闭经或诊断前年龄<25 岁的女性没有生育孩子。当分析至少有一个孩子的女性时,POI 女性的子女总数明显少于对照组(总体 2(1-3)与 2(2-4);P=0.017),当分析达到 45 岁的女性时(2(1-3)与 3(2-4);P=0.0073)。排除已知的供卵受孕妊娠,7.1%的 POI 女性在诊断后生育了孩子。POI 女性亲属的子女数量没有差异,包括家族性 POI 女性亲属。
局限性、谨慎的原因:由于无法确定女性在整个生育期是否一直在尝试怀孕或是否使用避孕措施,因此数据存在局限性。由于 POI 诊断后使用供卵的相关数据不完整,可能会略微高估未经辅助的受孕率。结果可能不适用于初产妇年龄较大或出生率较低的国家或州。
大约一半的 POI 女性在诊断前会生育子女。尽管 POI 女性生育的子女数量比年龄匹配的对照组少,但每位女性的子女数量差异为 1 个。这些数据表明,对于 25 岁或以上且继发性闭经的女性,在诊断为 POI 之前,生育能力可能不会受到影响。然而,诊断后怀孕的几率很低,我们证实的出生率<10%。生育子女数量较少的情况并没有延伸到亲属群体,这表明根据家族史预测 POI 可能很困难。
研究资金/利益冲突:本出版物中的工作得到了 R56HD090159 和 R01HD099487(C.K.W.)的支持。我们还通过国家癌症研究所的 P30 CA2014 部分支持犹他州人口数据库。内容仅由作者负责,不一定代表美国国立卫生研究院的官方观点。作者没有利益冲突。
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