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Association between maternal rheumatoid arthritis and small for gestational age neonates: a systematic review and
Lv Tian1,2, Zhiyuan Zhang2, Yuting Mao3
1Department of Rehabilitation, China-Japan Union Hospital of Jilin University, Changchun, China.
Insights
Maternal rheumatoid arthritis (RA) significantly increases the risk of offspring developing small for gestational age (SGA). This systematic review confirms the association, highlighting the need for further research into underlying mechanisms.
Area of Science:
- Obstetrics and Gynecology
- Rheumatology
- Perinatal Medicine
Background:
- Maternal rheumatoid arthritis (RA) is a potential risk factor for small for gestational age (SGA) offspring.
- Previous studies suggested an association, but lacked statistical significance.
- Clarifying the maternal RA-SGA link is vital for identifying adverse pregnancy outcomes and interventions.
Approach:
- A systematic literature search identified eligible studies up to August 2022.
- Quality assessment utilized the Newcastle-Ottawa scale, with heterogeneity assessed via Q and I² tests.
- Meta-analysis calculated Odds Ratios (ORs) with 95% Confidence Intervals (CIs), employing random or fixed effects models.
Key Points:
- Seven studies encompassing 12,323,918 participants were analyzed.
- A statistically significant association was found between maternal RA and SGA (OR = 1.70, 95% CI = 1.29-2.23, p < 0.001).
- Sensitivity analyses confirmed stable results, and publication bias was assessed as absent.
Conclusions:
- Maternal RA is definitively linked to an elevated risk of SGA in offspring.
- Further research is required to elucidate the specific biological mechanisms connecting maternal RA and SGA.
Background:
According to reports, maternal rheumatoid arthritis (RA) has been suggested as a possible adverse factor for developing small for gestational age (SGA) in offspring. However, some studies have also indicated a need for a more statistically significant association between the two. Understanding the relationship between maternal RA and the risk of SGA is crucial for identifying potential adverse outcomes and implementing appropriate interventions. Therefore, this study aims to elucidate the association between maternal RA and the risk of offspring developing SGA.
Methods:
This study was registered on the International Prospective Register of Systematic Reviews (PROSPERO) (ID: CRD42022357590). A systematic literature search was conducted to identify eligible studies up to August 2022. Quality assessment was performed according to the Newcastle-Ottawa scale. The Q test and I2 test tested and estimated heterogeneity among studies. Odds ratios (ORs) with 95% CI were calculated using random or fixed effects models depending on the heterogeneity. Subgroup analyses, sensitivity analyses, and publication bias assessments were also performed.
Results:
Seven studies, including 12,323,918 participants, were included in the analysis. The results showed a statistically significant association between maternal RA and SGA (OR = 1.70, 95% CI = 1.29-2.23, p < 0.001). Sensitivity analysis showed stable results. The funnel plot of the symmetric distribution and the results of Begg's and Egger's tests showed no publication bias.
Conclusion:
Maternal RA is associated with an increased risk of SGA in offspring. However, more studies are still needed to explore the potential mechanisms underlying maternal RA and SGA association.
Systematic Review Registration:
https://www.crd.york.ac.uk/PROSPERO/, identifier [CRD42022357590].
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