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胚胎植入前遗传学检测与儿童健康:一项全国注册登记研究。

Preimplantation genetic testing and child health: a national register-based study.

机构信息

Department of Obstetrics and Gynaecology, Institute of Clinical Sciences, Sahlgrenska Academy, Gothenburg University, East Hospital, Sahlgrenska University Hospital, Gothenburg, Sweden.

Department of Obstetrics and Gynaecology, Institute of Clinical Sciences, Sahlgrenska Academy, Gothenburg University, Reproductive Medicine, Sahlgrenska University Hospital, Gothenburg, Sweden.

出版信息

Hum Reprod. 2023 Apr 3;38(4):739-750. doi: 10.1093/humrep/dead021.

Abstract

STUDY QUESTION

Is preimplantation genetic testing (PGT) associated with adverse perinatal outcome and early childhood health?

SUMMARY ANSWER

Children born after PGT had comparable perinatal outcomes to children born after IVF/ICSI and comparable findings regarding early childhood health.

WHAT IS KNOWN ALREADY

PGT is offered to couples affected by monogenic disorders (PGT-M) or inherited chromosomal aberrations (PGT-SR), limiting the risk of transferring the disorder to the offspring. PGT, an invasive technique, requires genetic analysis of one or up to ten cells from the embryo and is combined with IVF or ICSI. Several studies, most of them small, have shown comparable results after PGT and IVF/ICSI concerning perinatal outcome. Only a few studies with limited samples have been published on PGT and childhood health.

STUDY DESIGN, SIZE, DURATION: We performed a register-based study including all singletons born after PGT (n = 390) in Sweden during 1 January 1996-30 September 2019. Singletons born after PGT were compared with all singletons born after IVF/ICSI (n = 61 060) born during the same period of time and with a matched sample of singletons (n = 42 034) born after spontaneous conception selected from the Medical Birth Register. Perinatal outcomes, early childhood health, and maternal outcomes were compared between pregnancies after PGT and IVF/ICSI as well as between pregnancies after PGT and spontaneous conception. Primary outcomes were preterm birth (PTB) and low birthweight (LBW) whereas childhood morbidity was the secondary outcome.

PARTICIPANTS/MATERIALS, SETTING, METHODS: Data on women who went through PGT and gave birth were obtained from the local databases at the two PGT centres in Sweden, whereas data on IVF treatment for the IVF/ICSI group were obtained from the national IVF registers. These data were then cross-linked to national health registers; the Medical Birth Register, the Patient Register, and the Cause of Death Register. Logistic multivariable regression analysis and Cox proportional hazards models were performed with adjustment for relevant confounders.

MAIN RESULTS AND THE ROLE OF CHANCE

The mean follow-up time was 4.6 years for children born after PGT and 5.1 years for children born after spontaneous conception, whereas the mean follow-up time was 9.0 years for children born after IVF/ICSI. For perinatal outcomes, PTB occurred in 7.7% of children after PGT and in 7.3% of children after IVF/ICSI, whereas the rates were 4.9% and 5.2% for LBW (adjusted odds ratio (AOR) 1.22, 95% CI 0.82-1.81 and AOR 1.17, 95% CI 0.71-1.91, respectively). No differences were observed for birth defects. In comparison to spontaneous conception, children born after PGT had a higher risk for PTB (AOR 1.73, 95% CI 1.17-2.58). Regarding early childhood health, the absolute risk of asthma was 38/390 (9.7%) in children born after PGT and 6980/61 060 (11.4%) in children born after in IVF/ICSI, whereas the corresponding numbers were 34/390 (8.7%) and 7505/61 060 (12.3%) for allergic disorders. Following Cox proportional hazards models, no significant differences were found for these outcomes. Sepsis, hypothyroidism, attention deficit hyperactivity disorder, autism spectrum disorders, mental retardation, cerebral palsy, and epilepsy were diagnosed in a maximum of three PGT children. No PGT children died during the follow-up period. Regarding maternal outcomes, the rates of placenta praevia and caesarean delivery were significantly higher after PGT in comparison to spontaneous conception (AOR 6.46, 95% CI 3.38-12.37 and AOR 1.52, 95% CI 1.20-1.92, respectively), whereas no differences were seen comparing pregnancies after PGT and IVF/ICSI.

LIMITATIONS, REASONS FOR CAUTION: The rather small sample size of children born after PGT made it impossible to adjust for all relevant confounders including fertilization method and culture duration. Moreover, the follow-up time was short for most of the children especially in the PGT group, probably lowering the absolute number of diagnoses in early childhood.

WIDER IMPLICATIONS OF THE FINDINGS

The results are reassuring and indicate that the embryo biopsy itself has no adverse effect on the perinatal, early childhood, or maternal outcomes. Although the results are comparable to IVF/ICSI also regarding early childhood outcome, they should be taken with caution due to the low number of children with diagnoses and short follow-up time. Long-term follow-up studies on children born after PGT are scarce and should be conducted considering the invasiveness of the technique.

STUDY FUNDING/COMPETING INTEREST(S): The study was financed by grants from the Swedish state under the agreement between the Swedish government and the county councils, the ALF-agreement (LUA/ALF 70940), the Board of National Specialised Medical Care at Sahlgrenska University Hospital and Hjalmar Svensson Research Foundation. There are no conflicts of interest to declare.

TRIAL REGISTRATION NUMBER

N/A.

摘要

研究问题

胚胎植入前遗传学检测(PGT)是否与围产期结局和儿童早期健康有关?

总结答案

PGT 后出生的儿童与 IVF/ICSI 后出生的儿童具有可比的围产期结局,并且在儿童早期健康方面也有类似的发现。

已知情况

PGT 是为受单基因疾病(PGT-M)或遗传性染色体异常(PGT-SR)影响的夫妇提供的,可降低将疾病传给后代的风险。PGT 是一种侵入性技术,需要对胚胎中的一个或最多十个细胞进行基因分析,并与 IVF 或 ICSI 结合使用。多项研究,其中大多数规模较小,表明 PGT 与 IVF/ICSI 相比,在围产期结局方面具有可比的结果。只有少数关于 PGT 和儿童健康的有限样本研究已经发表。

研究设计、规模、持续时间:我们进行了一项基于登记的研究,纳入了 1996 年 1 月 1 日至 2019 年 9 月 30 日期间在瑞典接受 PGT 后出生的所有 390 名单胎(PGT 组)。将 PGT 后出生的单胎与同期接受 IVF/ICSI 治疗后出生的所有 61060 名单胎(IVF/ICSI 组)和从医疗出生登记处选择的 42034 名自然受孕后出生的匹配单胎样本进行比较。比较 PGT 和 IVF/ICSI 后妊娠的早产(PTB)和低出生体重(LBW)等围产期结局、儿童早期健康和产妇结局,以及 PGT 和自然受孕后妊娠的儿童早期发病率。主要结局是早产和低出生体重,次要结局是儿童发病情况。

参与者/材料、设置、方法:接受 PGT 并分娩的女性数据来自瑞典两家 PGT 中心的当地数据库,而 IVF/ICSI 组的 IVF 治疗数据则来自国家 IVF 登记处。然后将这些数据与国家健康登记处交叉链接;医疗出生登记处、患者登记处和死因登记处。使用相关混杂因素进行调整后,进行逻辑多变量回归分析和 Cox 比例风险模型。

主要结果和机会作用

PGT 后出生的儿童平均随访时间为 4.6 年,自然受孕后出生的儿童平均随访时间为 5.1 年,而 IVF/ICSI 后出生的儿童平均随访时间为 9.0 年。对于围产期结局,PGT 后发生早产的比例为 7.7%,IVF/ICSI 后为 7.3%,而 LBW 的发生率分别为 4.9%和 5.2%(调整后的优势比(AOR)1.22,95%CI 0.82-1.81 和 AOR 1.17,95%CI 0.71-1.91)。未观察到出生缺陷差异。与自然受孕相比,PGT 后出生的儿童发生早产的风险更高(AOR 1.73,95%CI 1.17-2.58)。关于儿童早期健康,PGT 后出生的儿童哮喘的绝对风险为 38/390(9.7%),IVF/ICSI 后出生的儿童为 6980/61060(11.4%),而过敏疾病的相应数字为 34/390(8.7%)和 7505/61060(12.3%)。Cox 比例风险模型显示,这些结果没有显著差异。在 PGT 儿童中,最多诊断出 3 例败血症、甲状腺功能减退症、注意力缺陷多动障碍、自闭症谱系障碍、智力障碍、脑瘫和癫痫。在随访期间,没有 PGT 儿童死亡。关于产妇结局,与自然受孕相比,PGT 后胎盘前置和剖宫产的发生率明显更高(AOR 6.46,95%CI 3.38-12.37 和 AOR 1.52,95%CI 1.20-1.92),而与 IVF/ICSI 后相比,无差异。

局限性、谨慎的原因:PGT 后出生的儿童样本量较小,无法调整所有相关混杂因素,包括受精方法和培养时间。此外,大多数儿童的随访时间都很短,尤其是在 PGT 组中,这可能降低了早期儿童的诊断绝对数量。

更广泛的影响

结果令人放心,表明胚胎活检本身对围产期、儿童早期或产妇结局没有不良影响。尽管结果与 IVF/ICSI 相比在儿童早期结局方面也具有可比性,但由于诊断数量较少且随访时间较短,应谨慎对待。关于 PGT 后出生的儿童的长期随访研究很少,应考虑到该技术的侵入性进行研究。

研究资金/利益冲突:该研究由瑞典政府与县议会之间的协议、政府间协议(LUA/ALF 70940)、萨赫勒格伦斯卡大学医院和 Hjalmar Svensson 研究基金会资助的瑞典国家专项医疗保健拨款资助。没有利益冲突需要声明。

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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/220c/10068295/1cb9271a1d0d/dead021f1.jpg

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