- Research article
- Open Access
- Open Peer Review
Factors associated with ultrasound-aided detection of suboptimal fetal growth in a malaria-endemic area in Papua New Guinea
© Unger et al.; licensee BioMed Central. 2015
- Received: 9 September 2014
- Accepted: 19 March 2015
- Published: 3 April 2015
Fetal growth restriction (FGR) is associated with increased infant mortality rates and ill-health in adulthood. Evaluation of fetal growth requires ultrasound. As a result, ultrasound-assisted evaluations of causes of FGR in malaria-endemic developing countries are rare. We aimed to determine factors associated with indicators of abnormal fetal growth in rural lowland Papua New Guinea (PNG).
Weights and growth of 671 ultrasound-dated singleton pregnancies (<25 gestational weeks) were prospectively monitored using estimated fetal weights and birthweights. Maternal nutritional status and haemoglobin levels were assessed at enrolment, and participants were screened for malaria on several occasions. FGR was suspected upon detection of an estimated fetal weight or birthweight <10th centile (small-for-gestational age) and/or low fetal weight gain, defined as a change in weight z-score in the first quartile. Factors associated with fetal weight and fetal weight gain were additionally assessed by evaluating differences in weight z-scores and change in weight z-scores. Log-binomial and linear mixed effect models were used to determine factors associated with indicators of FGR.
SGA and low weight gain were detected in 48.3% and 37.0% of pregnancies, respectively. Of participants, 13.8%, 21.2%, and 22.8% had a low mid-upper arm circumference (MUAC, <22 cms), short stature (<150 cms) and anaemia (haemoglobin <90 g/L) at first antenatal visit. 24.0% (161/671) of women had at least one malaria infection detected in peripheral blood. A low MUAC (adjusted risk ratio [aRR] 1.51, 95% CI 1.29, 1.76, P < 0.001), short stature (aRR 1.27, 95% CI 1.04, 1.55, P = 0.009), and anaemia (aRR 1.27, 95% CI 1.06, 1.51, P = 0.009) were associated with SGA, and a low body mass index was associated with low fetal weight gain (aRR 2.10, 95% CI 1.62, 2.71, P < 0.001). Additionally, recent receipt of intermittent preventive treatment in pregnancy was associated with increased weight z-scores, and anaemia with reduced change in weight z-scores. Malaria infection was associated with SGA on crude but not adjusted analyses (aRR 1.13, 95% CI 0.95, 1.34, P = 0.172).
Macronutrient undernutrition and anaemia increased the risk of FGR. Antenatal nutritional interventions and malaria prevention could improve fetal growth in PNG.
- Malaria in pregnancy
- Fetal growth restriction
- Small for gestational age
- Mid-upper arm circumference
Fetal growth restriction (FGR) is associated with growth faltering in early childhood, increases infant mortality rates, and predisposes to ill-health in adulthood [1-4]. The burden of FGR and its potential consequence, low birthweight (LBW, <2,500 g), is estimated highest in low-income countries (LIC), where maternal undernutrition, short stature, malaria, anaemia, and HIV are important risk factors and pregnancy rates are high [3,5-7].
Researching causes of FGR in LICs is challenging because ultrasound for pregnancy dating and fetal growth monitoring is not yet widely available. Alternative estimators of gestational age such as last menstrual period are frequently unreliable , and late presentation to antenatal clinic precludes dating based on early pregnancy biometric measurements . A number of studies evaluated factors associated with measuring small-for-gestational-age (fetal size/weight <10th centile of a given weight standard, SGA) , commonly used as an indicator of FGR in epidemiological studies, yet few used ultrasound to determine gestational age and to evaluate fetal growth in utero.
Sequestration of Plasmodium falciparum-infected erythrocytes in the placental intervillous space is an important cause of LBW, most frequently due to FGR . A small number of ultrasound studies have evaluated the effect of malaria infection, and at times additional factors such as maternal nutritional status, on fetal growth. In Thailand and Brazil, P. falciparum and P. vivax infection in early pregnancy was associated with lower fetal biometric measurements [11,12], while in Tanzania, third trimester fetal growth alterations were observed following malaria infection before 20 weeks’ gestation . Infections tended to have most impact on growth in late second and early third trimester in a Kenyan cohort . In the Democratic Republic of Congo, a low mid-upper arm circumference (MUAC), short stature, malaria and anaemia were associated with SGA, , while in Thailand a low body mass index (BMI) was associated with reduced biparietal diameter z-scores . In another Congolese cohort, undernourished women were at increased risk of SGA due to P. falciparum infection . Overall, the number of ultrasound studies evaluating the role of undernutrition and malaria as causes of suboptimal fetal growth in LICs is limited, in particular outside of sub-Saharan Africa and South East Asia.
Antenatal care is a window of opportunity to improve fetal outcomes. Mapping principal causes of FGR in LICs provides a platform to develop, test and implement prenatal interventions to improve fetal growth and reduce LBW. We evaluated factors associated with FGR in fetuses of women co-enrolled in a randomised controlled trial evaluating intermittent preventive treatment of malaria in pregnancy (IPTp) in Papua New Guinea (PNG) (NCT01136850) . In the trial, IPTp reduced LBW by 26%, and reduced preterm birth by 38% .
We recruited women at first prenatal visit in Madang, PNG, between November 2009 and August 2012. The study area is characterised by year-round malaria transmission (P. falciparum and P. vivax) , and LBW is common (17%) .
Participants were co-enrolled in a trial that investigated the efficacy of monthly IPTp with azithromycin and sulphadoxine-pyrimethamine (SP), given from second trimester, compared to a single treatment course of SP plus chloroquine at their first prenatal visit, followed by monthly placebo doses (regimen designed to mimic current PNG prevention of malaria in pregnancy policy whilst allowing for participant blinding) . Eligibility criteria included age 16–49 years, singleton pregnancy, and no known co-morbidities. Only trial participants with a dating ultrasound <24 gestational weeks were included . Women with adverse pregnancy outcomes (miscarriage, stillbirth, congenital abnormality) were excluded from analyses.
At enrolment maternal sociodemographic and clinical characteristics were evaluated, maternal anthropometric measurements were taken, and women were screened for anaemia (haemoglobin [Hb] <90 g/L; HemoCue, Sweden). Anaemia was treated with iron/folate supplements and the anthelmintic albendazole, and malaria with quinine (first trimester) or artemether-lumefantrine, according to national guidelines, and insecticide-treated bed nets were provided when available.
A dating ultrasound scan (Logiqbook XP, General Electric Medical Systems, UK) was performed within a week of enrolment using crown-rump length or head circumference (femur length if unavailable) to estimate GA . To monitor fetal growth, women were scheduled for ultrasound scans every six weeks and followed up until birth when birthweight (BW) was measured to the nearest 10 g (Cupid digital scale, Charder Medical, Taiwan). Birth anthropometric measurements were included in analyses only if obtained within 24 hours of delivery. Ultrasound measurements were performed by two clinicians (MO, HWU) and fetal weights (EFW) were estimated from fetal head and abdominal circumference and femur length using standard formulae . A random selection of image stills (10%) was sent for quality control to JW. Women with an abnormal scan were referred to the local obstetrician for further management.
Maternal blood (enrolment, delivery, IPTp visits, passive case detection visits), and placental biopsies were used to characterise malarial infection. Thick smears were used to count the number of asexual parasites per 200 leukocytes (WBC) (or per 500 if <10 parasites/200 WBCs), assuming 8000 WBCs/μL of blood. Slides were declared negative if no parasite was seen in 200 oil-immersion fields at 1000 times magnification following reads by two microscopists. In addition, quantitative real-time polymerase chain reaction (qPCR) was performed on maternal blood . Placental malaria was classified as active (presence of parasitised cells) and past (hemozoin only) .
Given the detection of FGR is challenging and not all infants measuring are SGA are growth-restricted we opted to use two indicators of FGR, SGA (cross-sectional assessment) and low fetal weight gain (longitudinal assessment) . Suboptimal fetal growth was suspected upon detection of an EFW or BW below the 10th centile (SGA) of the Hadlock standard (10th centiles of ultrasound-estimated and birthweight-derived standards are similar at term) [19,22], and/or observation of low fetal weight gain, defined as a change in weight z-score (∆z) below the 25th centile of the overall distribution of ∆z, using weight measurements obtained >14 days apart. Factors associated with fetal weight and fetal weight gain were additionally assessed by evaluating differences in continuous outcomes measures, namely weight z-scores and ∆z.
Maternal macronutrient undernutrition was defined as low body mass index (BMI; <18.5 kg/m2) or low MUAC (<22 cm) at enrolment, and short stature as maternal height <150 cm . Weekly maternal weight gain was classified as low if in the first quartile for a subset of women with complete maternal weight gain data.
In addition to evaluating the effect of P. falciparum and P. vivax infection at enrolment (defined as positivity by light microscopy and/or qPCR) we generated weight measurement-specific time-dependent variables of infection to account for time and number of infections in relation to each weight measurement by pooling all available malaria diagnosis data (light microscopy, qPCR, histology) . ‘Recent infections’ were defined as infection during the interval from six weeks prior to the day of fetal weight measurement and ‘any infection’ as infection at any time up until and including the day of weight measurement. Women with active placental malaria were coded as a having had a ‘recent infection’ for the BW measurement, while women with past placental malaria were coded as having had an infection prior to or at enrolment provided they were peripheral blood negative throughout. ‘Recent IPTp’ was defined as IPTp ≤ 6 weeks before a weight measurement.
Statistical analyses were performed using Stata 12.0 (StataCorp, USA). For binary outcomes log-binomial regression models were fitted to calculate risk ratios (RR) and were estimated using generalised estimating equations (GEE) with an exchangeable working correlation structure. Linear mixed effect (LME) models with a restricted maximum likelihood were used to report mean differences in z-scores and ∆z. Both GEE and LME account for repeat measurements of indicators of FGR within individuals. Covariates associated with the outcome measure on univariate analysis (P <0.05) were used to generate adjusted RRs and mean differences. Interaction terms for indicators of maternal undernutrition (and gravidity) and malaria were included in log-binomial models to assess the potential effect measure modification of the malaria-SGA relationship by nutritional status and number of previous pregnancies, defined a priori as P <0.15 of the interaction term.
All participants provided written informed consent. The research was approved by the PNG Institute of Medical Research, the PNG Medical Research Advisory Council and the Melbourne Health Human Research Ethics Committee.
Characteristics of pregnant women and risk of measuring small-for-gestational age, Madang, PNG, 2009–2012
Betel nut consumption
Mother generating income
Partner generating income
Area of residence
Raised CRP at enrolment (≥5 mg/L)
Gestational week at fetal weight measurementb
A total of 1504 weight measurements were available for analysis (median per pregnancy 3, range 1–5; EFW = 893, BW = 611). 91.1% (611/671) of BWs were eligible for inclusion: the prevalence of LBW was 15.7% (96/611). Fetuses of 527 women had growth intervals available for analysis (median: 2, range 1–4, total = 833). Most weight measurements were obtained in mid-second and late third trimester (Table 1).
Ultrasound detection of SGA and low fetal weight gain, and association with measures at birth
Low fetal weight gainb
Normal fetal weight gainb
SGA at birth
Gestational age (wks)
39.1 (35.1, 42.1)
39.4 (34.4, 43.4)
2718 (2612, 2823)
2961 (2916, 3007)
2737 (2595, 2880)
2969 (2907, 3031)
Head circumference (cm)
32.5 (32.0, 33.0)
32.9 (32.8, 33.1)
32.7 (32.1, 33.2)
33.0 (32.7, 33.2)
Abdominal circumference (cm)
30.9 (30.3, 31.5)
31.8 (31.5, 32.0)
31.3 (30.4, 32.1)
31.8 (31.5, 32.1)
Crown-heel length (cm)
46.6 (45.8, 47.5)
47.7 (47.4, 48.1)
46.8 (45.8, 47.8)
47.4 (47.0, 47.9)
Ponderal index (g/[length in cm]3)
2.7 (2.6, 2.9)
2.8 (2.7, 2.8)
2.7 (2.5, 2.9)
2.8 (2.7, 2.9)
Cord haemoglobin (g/L)
132 (124, 141)
138 (135, 142)
134 (122, 146)
138.0 (133, 143)
Maternal characteristics and malaria infection, and associations with SGA and fetal weight z-scores
RR (95% CI) or coefficient [95% CI]
Adjusted RR (95% CI) or coefficient [95% CI]
Any malaria infection
1.36 (1.12, 1.65)
1.13 (0.95, 1.34)
−0.10 [−0.23, 0.03]
−0.06 [−0.19, 0.07]
Recent infection (<6 wks)
1.06 (0.80, 1.41)
1.03 (0.81, 1.32)
0.06 [−0.08, 0.20]
0.06 [−0.08, 0.21]
1.24 (1.00, 1.52)
1.12 (0.93, 1.34)
2.25 (1.63, 3.09)
1.18 (0.85, 1.63)
−0.09 [−0.22, 0.05]
−0.05 [−0.18, 0.09]
−0.25 [−0.53, 0.04]
−0.13 [−0.41, 0.16]
0.22 (0.17, 0.29)
0.79 (0.57, 1.08)
0.20 [0.12, 0.28]
0.16 [0.04, 0.27]
Low gestational weight gain
1.15 (0.92, 1.43)
1.21 (1.01, 1.45)b
−0.16 [−0.35, 0.03]
−0.18 [−0.37, 0.00]b
1.17 (0.92, 1.49)
1.12 (0.91, 1.36)
−0.13 [−0.30, 0.04]
−0.11 [−0.27, 0.05]
MUAC <22 cm
1.48 (1.20, 1.82)
1.51 (1.29, 1.76)
−0.19 [−0.36, −0.02]
−0.18 [−0.34, −0.01]
Body mass index <18.5 kg/m3
1.29 (0.98, 1.69)
1.33 (0.95, 1.86)
−0.19 [−0.36, −0.02]
−0.11 [−0.37, 0.16]
Height <150 cm
1.31 (1.10, 1.57)
1.27 (1.04, 1.55)
−0.19 [−0.36, −0.02]
−0.17 [−0.31, −0.03]
Haemoglobin <90 g/L
1.12 (0.92, 1.37)
1.27 (1.06, 1.51)
0.02 [−0.13, 0.16]
0.01 [−0.13, 0.15]
Maternal characteristics and malaria infection, and associations with low fetal weight and change in weight z-scores (∆z)
RR (95% CI) or coefficient [95% CI]
Adjusted RR (95% CI) or coefficient [95% CI]
Number of intervals
Episodes of low fetal weight gain
Malaria infection before interval
1.18 (0.87, 1.58)
1.13 (0.84, 1.52)
- 0.12 [−0.30, 0.06]
−0.11 [−0.29, 0.07]
Malaria infection during interval
1.08 (0.72, 1.62)
0.94 (0.62, 1.44)
−0.06 [−0.30, 0.17]
−0.04 [−0.28, 0.19]
1.18 (0.85, 1.63)
1.10 (0.79, 1.54)
−0.06 [−0.26, 0.14]
−0.04 [−0.24, 0.16]
MUAC <22 cm
1.22 (0.93, 1.59)
1.12 (0.93, 1.59)
−0.18 [−0.36, 0.01]
−0.16 [−0.34, 0.03]
Body mass index <18.5 kg/m3
2.10 (1.62, 2.71)
2.08 (1.62, 2.68)
−0.39 [−0.69, −0.08]
−0.35 [−0.66, −0.05]
Height <150 cm
1.26 (0.97, 1.63)
1.18 (0.92, 1.53)
−0.12 [−0.28, −0.04]
−0.09 [−0.25, 0.07]
Haemoglobin <90 g/L
1.18 (0.91, 1.52)
1.17 (0.91, 1.51)
−0.22 [−0.37, −0.06]
−0.18 [−0.34, −0.03]
A total of 197 Plasmodium spp. infections were detected in peripheral blood of 161 women (P. falciparum 70.3%, P. vivax 29.7%; median number of screens per participant: 4 [range 2–5]). Forty-four percent (86/197) of infections were submicroscopic (detected by qPCR only). Most peripheral infections were detected at enrolment (50.8% [100/197], prevalence 14.9%) and delivery (27.4% [54/197]), and 32 and 44 women had active and past placental infection, respectively.
A history of ‘any infection’ was significantly associated with an increased risk of measuring SGA in an unadjusted model (RR 1.36, 95% CI 1.12, 1.65, P = 0.002) but not in a fully adjusted model (RR 1.13, 95% CI 0.95, 1.34, P = 0.172) (Table 3). The risk of SGA increased with cumulative infections, but this association did not remain significant in adjusted analyses (Table 3). We did not observe effect measure modification of the malaria-SGA relationship by nutritional status (BMI or MUAC) or primigravidity.
In a cohort of pregnant PNG women maternal undernutrition, short stature and anaemia were associated with indicators of FGR. Malaria infection prior to a weight measurement was associated with an increased risk of SGA in unadjusted but not adjusted analyses. Recent receipt of IPTp was associated with increased fetal weight z-scores.
This is the first study to evaluate causes of FGR in a malaria-endemic region of PNG using ultrasound technology. Strengths of the study include a large sample size, sonographic pregnancy dating and availability of information on potential risk factors for FGR, including malaria.
This research needs to be interpreted in light of its limitations. First, the average number of EFWs measured per fetus was low as a result of higher-than-expected rates of participant non-attendance and limited availability of sonographers, and not all newborns had BWs collected within 24 hours of delivery. This may underestimate SGA prevalence, since fetal growth is thought to be pulsatile and catch-up growth may occur following an insult (e.g. treated malaria infection) . Second, we included BWs in the analysis and defined SGA as any weight below the 10th centile of the Hadlock standard. The use of this nomogram, derived from a Caucasian middle-class cohort, may overestimate SGA amongst differing ethnic groups, as may the inclusion of BWs . Third, despite efforts to closely monitor the malaria infection burden it is possible that infections were missed. Fourth, we used opportunistic sampling of our trial cohort for ultrasound studies, which may have introduced unintentional bias. Fifth, the trial setting (with different antimalarial regimes used) may have resulted in differential effects on parameters of interest. Lastly, not all possible risk factors of FGR and potential confounders of the observed relationships may have been measured and evaluated (e.g. HIV, helminth infection, micronutrient deficiencies).
AC is an important screening tool for FGR [25,26]. We used EFW rather than AC (or a combination of both) in our analyses for several reasons. First, it increases comparability of our findings with other malaria studies [13,16]. Second, many AC measurements were measured postnatally and not by ultrasound; they were not subject to the same stringent QC that ultrasound and birth weight measures were. Third, malaria in early pregnancy and undernutrition have been associated with reduced skeletal growth .
Indicators of maternal macronutritent undernutrition were strongly associated with low fetal weight or fetal weight gain. Interventions to improve maternal macronutrient nutritional status including nutritional supplementation merit evaluation in PNG and elsewhere . Anaemia at enrolment was associated with suboptimal fetal weight gain. Anaemia tended to be more common amongst women with concomitant malaria (29.9% vs 21.5%, P = 0.070) but nutritional deficiencies and intestinal helminth infections may also contribute to its aetiology. Although it has been proposed that iron supplementation may increase the risk of infection (including malaria) in iron-replete women , it is likely that most anaemic women in PNG are iron-deficient, and require supplementation.
We did not observe effect measure modification of the malaria-FGR relationship by maternal nutritional status , nor were we able to unequivocally demonstrate a deleterious effect of malaria infection on fetal growth unlike other studies : previous malaria infection was associated with SGA in unadjusted, but not adjusted analyses. This may be because we lack power due to low infection prevalence (reduced further following enrolment by both trial interventions) , and comparatively few malaria screening visits and weight measurements, thereby potentially missing infections or episodes of suboptimal fetal growth. Of malaria infections, many were submicroscopic, and their role in causing FGR and LBW remains poorly understood. P. vivax caused one third of infections in our cohort. Early P. vivax infection has been associated with reduced z-scores and anthropometric measurements  , but mechanisms are less well understood than for P. falciparum, and its deleterious effect on fetal growth may be smaller. Most infections were detected at enrolment. Although there is increasing evidence that malarial infection in early pregnancy can affect fetal growth , compensatory processes such as adaptive villous angiogenesis, and catch-up growth, may have mitigated the deleterious effect on fetal growth of some of these infections in the context of early treatment (trial intervention), insecticide-treated bed nets, and close clinical monitoring provided as part of the original trial [13,30]. The risk of SGA secondary to malaria became non-significant in models adjusting for GA at weight measurement. Inclusion of GA as a confounder was necessary because the risk of measuring small increased (linearly) as pregnancy progressed and GA at weight measurement differed between participants. Although we did not corroborate findings of other ultrasound studies, prevention and prompt treatment of malarial infection in pregnancy will reduce LBW and forms an essential part of prenatal care in malaria-endemic areas. Recent receipt of IPTp was associated with increased weight z-scores in this cohort, suggesting it (at least) temporarily prevents FGR through preventing and treating placental malaria or through other, unknown mechanisms that improve fetal growth.
Over 40% of pregnant women living in a malaria-endemic area in rural PNG had babies that measured SGA in utero or at delivery. Maternal macronutrient undernutrition, short stature and anaemia negatively affected fetal growth, while the low prevalence of malaria may explain its lack of influence on fetal growth. Antenatal interventions to improve nutritional status throughout pregnancy are likely to reduce the risk of FGR and LBW in PNG.
This research was supported by the Malaria in Pregnancy Consortium, through a grant from the Bill & Melinda Gates Foundation (46099); a PNGIMR Internal Competitive Research Award to MO, Pfizer Inc (investigator-initiated research grant WS394663), and the Pregvax Consortium, through a grant from the European Union’s Seventh Framework Programme FP7-2007-HEALTH (PREGVAX 201588). SK is supported through an NHMRC early career fellowship (GNT1052960), and IM received an NHMRC Senior Research Fellowship (#1043345). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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