A Systematic Review on Materno-Foetal Outcomes in Pregnant Women with IgA Nephropathy: A Case of "Late-Maternal" Preeclampsia?
Giorgina Barbara PiccoliIsabelle Annemijn KooijRossella AttiniBenedetta MontersinoFederica FassioMartina GerbinoMarilisa BiolcatiGianfranca CabidduElisabetta VersinoTullia TodrosPublished in: Journal of clinical medicine (2018)
The search retrieved 556 papers, of which 27 were included (13 series and 14 case-reports). The case series report on 581 women with 729 pregnancies. The analysis was performed in comparison to the available control groups: 562 non-pregnant controls were available for the analysis of progression of kidney disease. As for pregnancy related outcomes (preeclampsia (PE), pregnancy induced hypertension (PIH), preterm birth, small babies), we meta-analyzed the data with respect to the only series of low-risk pregnancies (1418 pregnancies). When compared with women who never got pregnant after diagnosis of IgA nephropathy, in the present meta-analysis pregnancy in women with IgA nephropathy was not associated with a higher risk of progression of kidney disease, possibly due to the overall preserved kidney function at baseline: end-stage kidney disease (OR 0.68; CI 0.28⁻1.65). Conversely, the incidence of adverse pregnancy-related outcomes was increased compared to low-risk controls: PE and PIH were more than ten-fold increased (OR 11.80; CI 7.53⁻18.48 and OR 10.39; CI 5.45⁻19.80), while the increase in risk of preterm birth and "low birth weight babies" was less marked (OR 3.37; CI 1.91⁻5.95 and OR 2.36; CI 1.52⁻3.66), a discrepancy suggesting the occurrence of "late" or "maternal" PE, that may affect less severely foetal growth or shorten gestation. In conclusion, in the present meta-analysis IgA nephropathy was not associated with an increased progression of kidney disease. The more than ten-fold increased risk of PIH and PE, in combination with a doubled risk of small babies, suggests the occurrence of "late" or "maternal" PE, usually less affecting early foetal growth. This finding may be of help in defining control policies, while further research is needed to guide clinical management.
Keyphrases
- preterm birth
- gestational age
- birth weight
- low birth weight
- pregnancy outcomes
- systematic review
- pregnant women
- human milk
- risk assessment
- meta analyses
- early onset
- public health
- blood pressure
- electronic health record
- type diabetes
- case control
- adverse drug
- randomized controlled trial
- high glucose
- drug induced
- endothelial cells
- machine learning
- glycemic control
- metabolic syndrome
- artificial intelligence
- cervical cancer screening