Investigating the Association of Assisted Reproduction Techniques and Adverse Perinatal Outcomes
Abstract
:1. Introduction
2. Materials and Methods
3. Results
3.1. Pre-Term Birth and Birthweight
3.2. Congenital and Chromosomal Defects
3.3. Hypospadias—Male Genital Anomalies
3.4. Heart and Metabolic Defects
4. Discussion
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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Year | Design | Sample | Outcome | Mean ± SD | CI | ||
---|---|---|---|---|---|---|---|
ART | Control Group | ||||||
Tommaso et al. [12] | 2010–2017 | Retrospective case–control study | 71 | 640 | No difference | ||
Simpson et al. [13] | 1997 | Prospective cohort study | 6077 | General population | No difference | ||
Marconi et al. [14] | 1991–2012 | Retrospective cohort study | 11.152 Blastocysts vs. 55.995 cleavages | General population | No difference at the risk of preterm birth | PTB: 1 (0.79–1.25) LBW: 0.92 (0.73–1.16) | 99.5% |
Sunkara et al. [15] | 1991–2011 | Retrospective cohort study | 584,835 Stimulated IVF cycles | 6168 unstimulated | No significant difference | PTB: 1.27 (0.8–2) LBW: 1.48 (0.9–2.42) | 95% |
Sunkara et al. [16] | 1996–2011 | Retrospective cohort study | 439 | 87.571 | No difference | PTB: 0.68 (0.46–0.99) LBW: 0.56 (0.37–0.85) | 95% |
Premru-Srsen T. et al. [17] | 2012–2015 | Retrospective case–control study | 333 | 1186 | Increased risk but not statistically significant | PTB: 1.07 (0.63–1.81) | 95% |
Scherrer et al. [18] | 2007–2010 | Prospective cohort study | 65 | 57 | No increase in PTB and LBW risk | ||
Szymusik et al. [19] | 2004–2014 | Retrospective case–control study | 336 | 308 | Increased risk for PTB and LBW | PTB (OR = 2.06; 1.16–3.68) LBW: (OR = 2.27; 1.19–4.36) | 95% |
Kaveh et al. [20] | 2004–2009 | Retrospective case–control study | 84 | 106 | Significant higher risk for preterm labor | PROM: 0.2 (0.07–0.8) LBW: 1.4 (0.6–3) | 95% |
Al-Fifi et al. [21] | 2003–2007 | Retrospective case–control study | 327 | 354 | Shorter birth date at ICSI group. | ||
Kamath et al. [22] | 1991–2011 | Retrospective case–control study | 5929 | 127.856 | Higher risk for PTB and LBW | PTB: 1.54 (1.34–1.80) LBW: 1.43 (1.24–1.66) | 99.5% |
Sunkara et al. [23] | 1991–2008 | Observational study | 65.868 live births after ART | General population | Significantly higher risk of PTB and LBW in the study | PTB: 1.15 (1.03–1.28) LBW: 1.17 (1.05–1.30) | 95% |
Year | Design | Sample | Outcome | Mean ± SD | CI | ||
---|---|---|---|---|---|---|---|
ART | Control Group | ||||||
Marconi et al. [14] | 1991–2012 | Retrospective cohort study | 11.152 Blastocyst-stage vs. 55.995 cleavage-stage | General population | 16% higher risk in blastocyst stage group | 0.9–1.49 | 99.5% |
Al-Fifi et al. [21] | 2003–2007 | Retrospective case–control Study | 327 | 354 | No difference for major defects | ||
Yuan et al. [24] | 2004–2020 | Retrospective cohort study | 1496 | 1396 | Slight but not statistically significant increase | 1.03 (0.71–1.5) | 95% |
Olson et al. [25] | 1989–2002 | Retrospective cohort study | 1805 | 8422 | Slightly higher rate of major birth defects | 1.30 (1–1.67) | 95% |
Luke et al. [26] | 2004–2017 | Population-based cohort study | 165.125 ART, 12.451 OI/IUI | 1.353.440 | Higher risk | 1.22–1.85 | 95% |
Fauque et al. [27] | 2013–2017 | Retrospective cohort study | 20.218 IUI, 45.303 fresh-ET 18.885 FET | 3.417.089 from NC | Increased risk in fresh-ET and FET group. | Fresh-ΕΤ: 1.15 (1.1–1.2) FET: 1.13 (1.05–1.21) | 95% |
Belva et al. [28] | 2004–2012 | Prospective clinical follow-up study | 1114 | General population | Abnormal fetal karyotype was found 41/1114 | 3.7% (2.7–4.9%) | 95% |
Jozwiak et al. [29] | 1997–2002 | Retrospective case–control study | 1136 | General population | No difference between ICSI group due to male factor and other subfertility issues | ||
Samli et al. [30] | 1996–2000 | Prospective cohort Study | 142 | General population | Increased rate of genetic defects in ICSI pregnancies |
Year | Design | Sample | Outcome | Mean ± SD | CI | ||
---|---|---|---|---|---|---|---|
ART | Control Group | ||||||
Simpson et al. [13] | 1997 | Prospective cohort Study | 6077 | General population | Increased risk for hypospadias | 2.9 (1.4–5.4) | 95% |
Silver et al. [32] | 1988–1994 | Retrospective case–control study | 14 | 14 | 5x higher risk in IVF group versus the control group | 1.46% IVF 0.27% control | |
Funke et al. [33] | 1999–2008 | Retrospective case–control study | 890 | 14316 | Increased risk for hypospadias; not cryptorchidism | 3.19 (1.266–8.042) | 95% |
Bang et al. [34] | 2008–2011 | Prospective cohort study | 7752 | General population | Increased risk in the ART group | 99 (1.3%) cryptorchidism 8 (0.1%) hypospadias 4(0.05%) both | |
Aliani et al. [35] | 2013–2015 | Prospective cross-sectional study | 5608 | General population | No relationship with infertility factor | 0.34% cryptorchidism 0.038% hypospadias |
Year | Design | Sample | Outcome | Mean ± SD | CI | ||
---|---|---|---|---|---|---|---|
ART | Control Group | ||||||
Scherrer et al. [18] | 2007–2010 | Prospective cohort study | 65 | 57 | ART group: 25% smaller brachial artery, 30% higher pulmonary artery pressure. | ||
Liu et al. [36] | 2015 | Prospective observational study | 100 | 100 | Higher rates in systolic and diastolic heart disorders | ||
Arx et al. [37] | 2015 | Prospective clinical trial | 54 | 54 | RV end-diastolic area significantly larger in study group; no difference in pulmonary artery pressure | ||
Ceelen et al. [38] | 1986–1995 | Retrospective cohort study | 233 | 233 | Higher body fat percentage in study group | ||
Ceelen et al. [39] | 1986–1995 | Retrospective cohort study | 1313 | 131 | Elevated rates of BP and blood glucose in ART group | Systolic BP: 2.1 (1.4–3.3) Diastolic: 1.9 (1.2–3) | 95% |
Sakka et al. [40] | 2010 | Prospective case–control study | 106 | 68 | Higher systolic and diastolic BP and TRG. |
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Potiris, A.; Perros, P.; Drakaki, E.; Mavrogianni, D.; Machairiotis, N.; Sfakianakis, A.; Karampitsakos, T.; Vrachnis, D.; Antonakopoulos, N.; Panagopoulos, P.; et al. Investigating the Association of Assisted Reproduction Techniques and Adverse Perinatal Outcomes. J. Clin. Med. 2024, 13, 328. https://doi.org/10.3390/jcm13020328
Potiris A, Perros P, Drakaki E, Mavrogianni D, Machairiotis N, Sfakianakis A, Karampitsakos T, Vrachnis D, Antonakopoulos N, Panagopoulos P, et al. Investigating the Association of Assisted Reproduction Techniques and Adverse Perinatal Outcomes. Journal of Clinical Medicine. 2024; 13(2):328. https://doi.org/10.3390/jcm13020328
Chicago/Turabian StylePotiris, Anastasios, Paraskevas Perros, Eirini Drakaki, Despoina Mavrogianni, Nikolaos Machairiotis, Antonios Sfakianakis, Theodoros Karampitsakos, Dionysios Vrachnis, Nikolaos Antonakopoulos, Periklis Panagopoulos, and et al. 2024. "Investigating the Association of Assisted Reproduction Techniques and Adverse Perinatal Outcomes" Journal of Clinical Medicine 13, no. 2: 328. https://doi.org/10.3390/jcm13020328
APA StylePotiris, A., Perros, P., Drakaki, E., Mavrogianni, D., Machairiotis, N., Sfakianakis, A., Karampitsakos, T., Vrachnis, D., Antonakopoulos, N., Panagopoulos, P., Drakakis, P., & Stavros, S. (2024). Investigating the Association of Assisted Reproduction Techniques and Adverse Perinatal Outcomes. Journal of Clinical Medicine, 13(2), 328. https://doi.org/10.3390/jcm13020328