Glinianaia Svetlana V, Tennant Peter W G, Rankin Judith
Institute of Health & Society, Newcastle University, Baddiley-Clark Building, Richardson Road, Newcastle upon Tyne, NE2 4AX, UK.
School of Healthcare, University of Leeds, Baines Wing (Room 1.11), Leeds, LS2 9JT, UK.
BMC Med. 2017 Jan 31;15(1):20. doi: 10.1186/s12916-017-0789-5.
Recurrence risks for familial congenital anomalies in successive pregnancies are known, but this information for major structural anomalies is lacking. We estimated the absolute and relative risks of recurrent congenital anomaly in the second pregnancy for women with a history of a congenital anomaly in the first pregnancy, for all major anomaly groups and subtypes.
Population-based register data on 18,605 singleton pregnancies affected by major congenital anomaly occurring in 872,493 singleton stillbirths, live births and terminations of pregnancy for fetal anomaly were obtained from the Northern Congenital Abnormality Survey, North of England, UK, for 1985-2010. Absolute risks (ARs) and relative risks (RRs) for recurrent congenital anomaly (overall, from a similar group, from a dissimilar group) in the second pregnancy were estimated by history of congenital anomaly (overall, by group, by subtype) in the first pregnancy.
The estimated prevalences of congenital anomaly in first and second pregnancies were 275 (95% CI 270-281) and 163 (95% CI 159-168) per 10,000 respectively. For women whose first pregnancy was affected by congenital anomaly, the AR of recurrent congenital anomaly in the second pregnancy was 408 (95% CI 365-456) per 10,000, 2.5 (95% CI 2.3-2.8, P < 0.0001) times higher than for those with unaffected first pregnancies. For similar anomalies, the recurrence risk was considerably elevated (RR = 23.8, 95% CI 19.6-27.9, P < 0.0001), while for dissimilar anomalies the increase was more modest (RR = 1.4, 95% CI 1.2-1.6, P = 0.001), although the ARs for both were 2%.
Absolute recurrence risks varied between 1 in 20 and 1 in 30 for most major anomaly groups. At pre-conception and antenatal counselling, women whose first pregnancy was affected by a congenital anomaly and who are planning a further pregnancy may find it reassuring that, despite high relative risks, the absolute recurrence risk is relatively low.
已知连续妊娠中家族性先天性异常的复发风险,但缺乏关于主要结构异常的此类信息。我们估计了首次妊娠有先天性异常病史的女性在第二次妊娠中复发先天性异常的绝对风险和相对风险,涵盖所有主要异常组和亚型。
从英国英格兰北部先天性异常调查中获取了1985 - 2010年基于人群登记的数据,涉及872,493例单胎死产、活产及因胎儿异常而终止妊娠的情况,其中18,605例单胎妊娠受主要先天性异常影响。根据首次妊娠的先天性异常病史(总体、按组、按亚型)估计第二次妊娠中复发先天性异常(总体、来自相似组、来自不同组)的绝对风险(ARs)和相对风险(RRs)。
首次和第二次妊娠中先天性异常的估计患病率分别为每10,000例中有275例(95%可信区间270 - 281)和163例(95%可信区间159 - 168)。对于首次妊娠受先天性异常影响的女性,第二次妊娠中复发先天性异常的AR为每10,000例中有408例(95%可信区间365 - 456),比首次妊娠未受影响的女性高2.5倍(95%可信区间2.3 - 2.8,P < 0.0001)。对于相似异常,复发风险显著升高(RR = 23.8,95%可信区间19.6 - 27.9,P < 0.0001),而对于不同异常,增加幅度较小(RR = 1.4,95%可信区间1.2 - 1.6,P = 0.001),尽管两者的AR均为2%。
大多数主要异常组的绝对复发风险在20分之一到30分之一之间。在孕前和产前咨询时,首次妊娠受先天性异常影响且计划再次妊娠的女性可能会感到安心,即尽管相对风险较高,但绝对复发风险相对较低。