TABLE 1.
Study type |
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Observational |
RCT |
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Health outcome | Mechanistic: in vitro | Retrospective | Case control2 | Prospective | Primary | Secondary | Nature of evidence based on iron exposure indicator | |
GDM/T2D-PP3 | —4 | √ | √ | √ | √ | Supplementation: inconsistent5 SF concentration: consistent;6 intake: inconsistent |
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Preterm birth7 | √ | √ | √ | Hemoglobin concentration: inconsistent across trimesters SF concentration; consistent |
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Impaired fetal growth8 | √ | √ | √ | Supplementation: consistent; hemoglobin concentration: inconsistent across trimesters SF concentration: inconsistent |
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Impaired infant/child growth9 | √ | Supplementation to iron replete: consistent | ||||||
Long-term impaired cognitive development10 | √ | Supplementation to iron replete: limited | ||||||
Diarrhea11 | √ | √ | Supplementation or fortification: inconsistent | |||||
Intermediate outcome | ||||||||
Microbiome change12 | √ | √ | √ | Supplementation: inconsistent |
A check (√) indicates available evidence for each study type. GDM, gestational diabetes mellitus; RCT, randomized controlled trial; SF, serum ferritin; T2D-PP, type 2 diabetes postpartum.
Includes nested studies.
Only one animal study (rats) on high-fructose diet induced GDM; there was no additional effect on GDM with a moderate 83% increase in dietary iron (49).
Inconsistent indicates discordant results. In this case, discordant results for supplemental iron and GDM from observational studies and RCT.
Consistent indicates concordant results. In this case, concordant results reported associating SF with GDM risk from observational studies.
From reference 61.
From reference 62.