The choice of reference chart affects the strength of the association between malaria in pregnancy and small for gestational age: an individual participant data meta-analysis comparing the Intergrowth-21 with a Tanzanian birthweight chart

The prevalence of small for gestational age (SGA) may vary depending on the chosen weight-for-gestational-age reference chart. An individual participant data meta-analysis was conducted to assess the implications of using a local reference (STOPPAM) instead of a universal reference (Intergrowth-21)...

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Published inMalaria journal Vol. 21; no. 1; p. 292
Main Authors Mtove, George, Minja, Daniel T R, Abdul, Omari, Gesase, Samwel, Maleta, Kenneth, Divala, Titus H, Patson, Noel, Ashorn, Ulla, Laufer, Miriam K, Madanitsa, Mwayiwawo, Ashorn, Per, Mathanga, Don, Chinkhumba, Jobiba, Gutman, Julie R, Ter Kuile, Feiko O, Møller, Sofie Lykke, Bygbjerg, Ib C, Alifrangis, Michael, Theander, Thor, Lusingu, John P A, Schmiegelow, Christentze
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 12.10.2022
BioMed Central
BMC
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Summary:The prevalence of small for gestational age (SGA) may vary depending on the chosen weight-for-gestational-age reference chart. An individual participant data meta-analysis was conducted to assess the implications of using a local reference (STOPPAM) instead of a universal reference (Intergrowth-21) on the association between malaria in pregnancy and SGA. Individual participant data of 6,236 newborns were pooled from seven conveniently identified studies conducted in Tanzania and Malawi from 2003-2018 with data on malaria in pregnancy, birthweight, and ultrasound estimated gestational age. Mixed-effects regression models were used to compare the association between malaria in pregnancy and SGA when using the STOPPAM and the Intergrowth-21 references, respectively. The 10th percentile for birthweights-for-gestational age was lower for STOPPAM than for Intergrowth-21, leading to a prevalence of SGA of 14.2% and SGA of 18.0%, p < 0.001. The association between malaria in pregnancy and SGA was stronger for STOPPAM (adjusted odds ratio (aOR) 1.30 [1.09-1.56], p < 0.01) than for Intergrowth-21 (aOR 1.19 [1.00-1.40], p = 0.04), particularly among paucigravidae (SGA aOR 1.36 [1.09-1.71], p < 0.01 vs SGA aOR 1.21 [0.97-1.50], p = 0.08). The prevalence of SGA may be overestimated and the impact of malaria in pregnancy underestimated when using Intergrowth-21. Comparing local reference charts to global references when assessing and interpreting the impact of malaria in pregnancy may be appropriate.
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ISSN:1475-2875
1475-2875
DOI:10.1186/s12936-022-04307-2