Lifestyle interventions for overweight and obese pregnant ... · Eugene Oteng-Ntim1,2,3*, Rajesh...
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RESEARCH ARTICLE Open Access
Lifestyle interventions for overweight and obesepregnant women to improve pregnancyoutcome: systematic review and meta-analysisEugene Oteng-Ntim1,2,3*, Rajesh Varma1,3, Helen Croker4, Lucilla Poston3 and Pat Doyle2
Abstract
Background: Overweight and obesity pose a big challenge to pregnancy as they are associated with adversematernal and perinatal outcome. Evidence of lifestyle intervention resulting in improved pregnancy outcome isconflicting. Hence the objective of this study is to determine the efficacy of antenatal dietary, activity, behaviour orlifestyle interventions in overweight and obese pregnant women to improve maternal and perinatal outcomes.
Methods: A systematic review and meta-analyses of randomised and non-randomised clinical trials following priorregistration (CRD420111122 http://www.crd.york.ac.uk/PROSPERO) and PRISMA guidelines was employed. A search ofthe Cochrane Library, EMBASE, MEDLINE, CINAHL, Maternity and Infant care and eight other databases for studiespublished prior to January 2012 was undertaken. Electronic literature searches, study selection, methodology andquality appraisal were performed independently by two authors. Methodological quality of the studies was assessedaccording to Cochrane risk of bias tool. All appropriate randomised and non-randomised clinical trials were includedwhile exclusions consisted of interventions in pregnant women who were not overweight or obese, had pre-existingdiabetes or polycystic ovarian syndrome, and systematic reviews. Maternal outcome measures, including maternalgestational weight gain, gestational diabetes and Caesarean section, were documented. Fetal outcomes, includinglarge for gestational age and macrosomia (birth weight > 4 kg), were also documented.
Results: Thirteen randomised and six non-randomised clinical trials were identified and included in the meta-analysis. The evidence suggests antenatal dietary and lifestyle intervention in obese pregnant women reducesmaternal pregnancy weight gain (10 randomised clinical trials; n = 1228; -2.21 kg (95% confidence interval -2.86 kgto -1.59 kg)) and a trend towards a reduction in the prevalence of gestational diabetes (six randomised clinicaltrials; n = 1,011; odds ratio 0.80 (95% confidence interval 0.58 to 1.10)). There were no clear differences reported forother outcomes such as Caesarean delivery, large for gestational age, birth weight or macrosomia. All availablestudies were assessed to be of low to medium quality.
Conclusion: Antenatal lifestyle intervention is associated with restricted gestational weight gain and a trendtowards a reduced prevalence of gestational diabetes in the overweight and obese population. These findingsneed to be interpreted with caution as the available studies were of poor to medium quality.
BackgroundBoth developed and developing countries are experien-cing a rapid increase in the prevalence of obesity [1-3].In the UK, 24% of women of reproductive age are nowobese (body mass index (BMI) equal or greater than
30 kg/m2) and the prevalence appears to be increasing[4]. Studies in UK women show that the rates of obesityin pregnancy have almost doubled in the last two dec-ades [5,6]. Recent estimates suggest the prevalence ofobesity in pregnancy in the UK is at least 20% with 5%having severe or morbid obesity [7,8].Observational study data has linked obesity in preg-
nancy with adverse maternal and infant outcomes[7-10]. Obesity increases the risks of gestational diabetes[8,10-12], hypertensive disease (including pre-eclampsia)
* Correspondence: [email protected] of Women’s Health, Guy’s and St Thomas’ NHS FoundationTrust (King’s Health Partners), St Thomas’ Hospital, Westminster Bridge Road,London, SE 1 7EH, UKFull list of author information is available at the end of the article
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© 2012 Oteng-Ntim et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the CreativeCommons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, andreproduction in any medium, provided the original work is properly cited.
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[8,13,14], thromboembolism [15,16], infection [14,17],Caesarean section [8,18], congenital fetal anomalies [19],macrosomia [13], induction [20], stillbirth [12], shoulderdystocia [14] and preterm delivery [21]. Moreover,maternal obesity may impact on long-term outcomessuch as the increasing weight of the child in infancyand the severity of obesity in future generations[10,22,23].As most of the adverse outcomes of obese pregnancies
show strong associations with pre-pregnancy BMI, it isreasonable to assume that the ideal intervention wouldbe to reduce obesity prior to pregnancy [24]. However,this is difficult to achieve because 50% of pregnancies inthe UK are unplanned and a recent study concludedthat only a small proportion of women planning preg-nancy follow nutrition and lifestyle recommendations[25]. As such, an intervention pre-pregnancy may reachonly a small proportion of the intended women.Alternatively, pregnancy itself may represent an ideal
opportunity to target lifestyle change as women haveincreased motivation to maximise their own health andthat of their unborn child [25]. However, evidence ofbenefit from published intervention studies appears lim-ited and inconsistent [26-44]. We therefore sought todetermine the efficacy of combined dietary activity andbehaviour support interventions in overweight andobese pregnant women by undertaking a systematicreview and meta-analysis according to PRISMA (Trans-parent Reporting of Systematic Reviews and Meta-ana-lyses) criteria for maternal clinical outcomes of weightgain, gestational diabetes and Caesarean section andinfant outcomes, such as large for gestational age andmacrosomia. Our aim was to generate data of the high-est statistical power and sensitivity. Hence, in compari-son with previous similar themed systematic reviews[45-48], we chose to interrogate multiple databases (notrestricted to English) and also separately meta-analyserandomised clinical trials (RCTs) and non-RCTs evalu-ating relevant clinical outcomes, including gestationaldiabetes and Caesarean section, which had not beenattempted in prior meta-analyses.
MethodsEligibility criteriaThe eligible studies included RCTs and non-RCTs thatevaluated antenatal dietary and lifestyle interventions inobese and overweight pregnant women whose outcomemeasures included quantitative maternal and fetal healthoutcomes. Systematic reviews and trials of women withexisting gestational diabetes, or trials of pre-conceptionor postpartum interventions, were not included. Inclu-sion of trials was not restricted by language, publicationdate or country. Systematic reviews and observationalstudies were excluded.
Information sourcesLiterature searches were performed using five mainstreamelectronic databases (Cochrane Library, MEDLINE,EMBASE, CINAHL, Maternity and Infant care), and eightother databases (PsyclINFO via OVID SP, PyscLNFO viaOVID SP, Science Citation Index via Web of Science,Social Science Citation Index via Web of Science, GlobalHealth, Popline, Medcarib, Nutrition database).
Search strategyThe following MeSH terms, words and combinations ofwords, were used in constructing the systematic search:overweight OR obesity; pregnancy OR pregnancy com-plications OR pregnancy outcome OR prenatal care,prenatal, antenatal, intervention, randomised controlledtrial, life style, “early intervention (education)”, healtheducation, education, patient education handout, patienteducation, exercise, exercise therapy, health promotion,diet, carbohydrate-restricted, diet, fat-restricted, diet,reducing, diet therapy, weight loss. Full details of thesearch strategy are shown in Table 1. The searches wereunlimited by time up to January 2012 and limited tohuman studies and clinical trials. The systematic searchwas undertaken in the mainstream databases and tar-geted searches were conducted in the other databases.
Study selectionElectronic literature searches, study selection, methodol-ogy, appropriateness for inclusion and quality appraisalwere performed independently and in duplicate by twoauthors (E-ON and RV). Disagreements betweenreviewers were resolved by consensus. Included studieswere divided into two groups (RCTs and non-RCTs)and separately meta-analysed.
Data collection processTwo independent reviewers extracted the data. As a firststep, each paper was screened using the title and theabstract. In the next round, studies were assessed for meth-odological quality and appropriateness for inclusion by tworeviewers working independently from the full text of themanuscript. This was done without consideration of theresults.
Data itemsFor each included trial, data was extracted on maternalgestational weight gain; gestational diabetes; Caesareansection; large for gestational age baby (> 4 kg); and birthweight. The included studies have been summarised inTables 2 and 3.
Risk of bias in individual studiesThe quality of studies was assessed based on how thestudies had minimised bias and error in their methods.
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We categorised the studies according to criteria basedon PRISMA guidelines [49] and the Cochrane Library[50]. For example, high quality trials reported studyaims; control comparison similar to the interventiongroup; relevant population demographics pre- and post-intervention; and data on each outcome. These studycharacteristics are tabulated in Tables 4 and 5. A finalassessment categorised the studies as high, medium orlow quality.
Summary and analysis of studies that meet the criteriaThis is shown in Figure 1 and in a tabulated formatcontained within Table 2 and 3.
Summary measures and data synthesisThe main measure of effect of the meta-analysis was theodds ratio or standardised mean difference. The datasyntheses were conducted according to the Cochranemethodology [50]. First, we used statistical meta-analysistechniques to assess the efficacy of the interventions ofcontrolled trials. Chi-square statistics tests were used totest for heterogeneity (Q statistics) between controlledtrials. When there was no significant heterogeneity, wecombined effect sizes in a fixed effect statistical meta-ana-lysis using Review Manager (RevMan; Version 5.0,
Copenhagen: The Nordic Cochrane Centre, The CochraneCollaboration, 2008). The meta-analyses were performedby calculating the odds ratios (for proportion data) orstandardised mean differences (for scale data) using afixed effects model. Quantitative analysis was performedon an intention-to-treat basis focused on data derivedfrom the period of follow-up. There was heterogeneitybetween studies because of the smaller sample size ofsome of the studies (poor quality), variation of the studypopulation and the intensity and duration of the interven-tional strategies being evaluated. A random effects modelwas used to adjust for heterogeneity.
ResultsStudy characteristicsThe review process is outlined in Figure 1 and theselected papers summarised in Tables 2 and 3.Fifteen trials met the inclusion criteria: 13 RCTs
[26-34] and six non-RCTs [35,36,38,39,51,52]. All 19trials were performed in developed countries: five in theUSA, three in Canada, three in Australia, two in Finlandand one in Denmark, Netherlands, Sweden, Spain, Braziland Belgium (Tables 2 and 3). Five RCTs were judgedto be of medium quality [27,29,34]. The rest weredeemed low quality (Tables 4 and 5).
Table 1 Search strategy utilised for MEDLINE 1946 to January 2012
Batch Search term (MESH) Combination Result
1 Pregnancy Complications/OR Pregnancy/OR PregnancyOutcome/OR Pregnancy, High Risk/
646,055
2 Prenatal Care/OR Pregnancy/OR Pregnancy Complications 647,726
3 Antenatal.mp. 18,393
4 Gestation intervention.mp. 4
5 1 OR 2 OR 3 OR 4 651,321
6 Overweight.mp. OR Obesity/OR Overweight/OR Body Weight/ 249,097
7 Obesity/OR Obesity, Morbid/or Obesity.mp. 145,882
8 Body Weight/OR Obesity/OR Body Mass Index/or BMI.mp. OROverweight/
293,584
9 6 OR 7 OR 8 328,089
10 5 AND 9 21,583
11 Diet, Fat-Restricted/OR Diet/OR Diet, Protein-Restricted/OR Diet,Carbohydrate-Restricted/OR Diet.mp. OR Diet, Reducing/ORDiet Therapy/
255,985
12 Life Style/ 36,837
13 Health Education/ 48,625
14 Patient Education as Topic/ 63,238
15 Exercise.mp. OR Exercise/OR Exercise, Therapy/ 192,937
16 Health Promotion/ 43,967
17 Weight Loss/ 19,434
18 11 OR 12 OR 13 OR 14 OR 15 OR 16 OR 17 601,919
19 10 AND 18 3,769
20 LIMIT 19 TO ((female or humans or pregnancy) and (clinical trial,all OR clinical trial, phase i OR clinical trial, phase ii OR clinical trial,phase iii OR clinical trial, phase iv OR clinical trial OR controlledclinical trial OR randomized controlled trial))
154
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Table 2 A summary of the studies that met the criteria of the systematic review on lifestyle interventions in overweight and obese pregnant women:randomised trials
Author(year)
Ethnic group/Country
Participant/setting Sample size Intervention Outcome measure(s)
Conclusion
Polley et al.(2002) [32]
31% black and61% white/USA
Recruited before 20 weeks of pregnancy(normal BMI > 19.5 to 24.9; overweightBMI ≥ 25 to < 30 kg/m2)/Hospital based
120, including49 overweight59 in controlarm; 61 ininterventionarm
Exercise and nutrition information (oral andnewsletter) Personalised graphs andbehavioural counselling.
Gestational weightgain; gestationaldiabetes; Caesareansection; birthweight
No statistically significant reduction ingestational weight, prevalence ofgestational diabetes, Caesareansection, or large for gestational agebaby
Hui et al.(2006) [33]
PredominantlyCaucasian/Canada
Less than 26 weeks pregnant (communitybased and antenatal clinics). All BMIcategories. Mean BMI of non-interventionarm = 25.7 (SD = 6.3) and forintervention arm = 23.4(SD = 3.9)
4521 in non-interventionarm; 24 ininterventionarm
Physical exercise (group-sessions home-based exercise)Individualized nutrition plans
Gestational weightgain
No statistically significant reduction ingestational weight gain
Wolff et al.,2008 [30]
100%Caucasian/Denmark
Obese (BMI ≥ 30 kg/m2) women enrolledat 15 weeks’ gestation
50 analysed23 in controlarm; 27 ininterventionarm
Intensive intervention with 10 one-hourvisits with a dietician at each antenatal visit,dietary guidance provided
Gestational weightgain; gestationaldiabetes; Caesareansection; birthweight
Statistically significant reduction ingestational weight gain, nostatistically significant reduction inprevalence of gestational diabetes orCaesarean section, or birthweight
Jeffries et al.,2009 [28]
> 90%Caucasian/Australia
Women at or below 14 weeks’ gestation.All BMI categories included
286138 in controlarm; 148 ininterventionarm
Personalised weight measurement card(based on Institute of Medicine guidelines).Control had only single measurement atenrolment
Gestational weightgain
No statistically significant reduction ingestational weight gain.
Ong et al.,2009 [42]
PredominantlyCaucasian/Australia
Pregnant obese women recruited at 18weeks’ gestation
12six in controlarm; six ininterventionarm
Personalised 10 weeks of home-basedsupervised exercise (three sessions perweek)
Maternal aerobicfitness andgestational diabetes
No statistically significant difference inaerobic fitness or gestational diabetes
Barakat etal., 2011 [41]
100%Caucasian/Spain
All BMI categories 16080 in controlarm; 80 ininterventionarm
Three group-based sessions per week, lightresistance and toning exercise from thesecond trimester
Gestational weightgain andbirthweight
No statistically significant difference ingestational weight gain and birthweight. Exercise intervention mightattenuate adverse consequences ofmaternal BMI on newborn birth size
Asbee et al.,2009 [27]
26% AfricanAmerican/USA
Pregnant women recruited before 16weeks’ gestation. All BMI categoriesexcept those of BMI > 40 kg/m2
10043 in controlarm; 53 ininterventionarm
One session of dietetic counselling andactivity
Gestational weightgain; pregnancyoutcome
Statistically significant reduction ingestational weight gain. No effect onpregnancy outcome
Thornton etal., 2009 [29]
41% AfricanAmerican/USA
Obese pregnant women (BMI ≥ 30 kg/m2) recruited between 12 and 28 weeks’gestation
257randomised.25 lost tofollow up. 116in controlarm; 116 ininterventionarm
Nutritional regime for gestational diabetes Gestational weightgain; gestationaldiabetes; Caesareansection; pregnancyoutcome
Statistically significant reduction ingestational weight gain, nostatistically significant reduction inprevalence of gestational diabetes,Caesarean section or birthweight
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Table 2 A summary of the studies that met the criteria of the systematic review on lifestyle interventions in overweight and obese pregnant women: rando-mised trials (Continued)
Guelinckx etal., 2010 [26]
100%Caucasian/Belgium
Obese (BMI > 30 kg/m2) women enrolledat 15 weeks’ gestation.
195randomised85 analysed65 in controlarm; 65 inpassive arm,65 ininterventionarm
Three arms: group sessions with a dietician;written brochures; and standard careDietary and physical activity guidanceprovided by dietician and in writtenbrochures
Nutritional habits;gestational weightgain; gestationaldiabetes; Caesareansection; birthweight
Improved nutritional habits; nostatistically significant reduction ingestational weight gain, prevalence ofgestational diabetes, Caesareansection or birthweight.
Phelan etal., 2011 [34]
67% White/USA
Pregnant women BMI between 19.8 and40 kg/m2 recruited between 10 and 16weeks’ gestation
401randomised.201 in non-interventionarm; 200 ininterventionarm
Exercise and nutrition information (oral andnewsletter) Personalised graphs andbehavioural counselling
Gestational weightgain; gestationaldiabetes; Caesareansection; pregnancyoutcome
Significant reduction in gestationalweight gain; no statistically significantreduction in prevalence of gestationaldiabetes, Caesarean section orbirthweight
Quinlivan etal., 2011 [59]
73% white,19% Asian/Australia
Pregnant women: overweight (BMI 25 to29.9 kg/m2) and obese (BMI ≥ 30 kg/m2)
132randomised.65 in non-interventionarm; 67 ininterventionarm
Attended a study- specific antenatal clinicproviding continuity of care, weighing onarrival, brief dietary intervention by foodtechnologist and psychological assessmentand intervention if indicated
Gestational weightgain; gestationaldiabetes;birthweight
Statistically significant reduction ingestational weight gain andprevalence of gestational weight gain.No statistically significant reduction inbirthweight.
Luoto et al.,2011 [43]
Predominantlywhite/Finland
Pregnant women at risk of gestationaldiabetes. All BMI ranges
399 clusterrandomised.219 in non-interventionarm; 180 ininterventionarm
Attended a study-specific individualantenatal lifestyle counselling clinicincluding group exercise
Gestationaldiabetes;gestational weightgain; birthweight
Statistically significant reduction inbirthweight and macrosomia but nostatistically significant difference ingestational diabetes
Nascimentoet al., 2011[44]
Predominantlywhite/Brazil
Pregnant women of all BMI categories 82randomised.42 in non-interventionarm; 40 ininterventionarm
Attended a group-based exercise undersupervision and received a home exercisecounselling
Gestational weightgain; raised bloodpressure; perinataloutcome
No statistically significant difference ingestational weight gain in terms ofgestational weight gain, raised bloodpressure or perinatal outcome
BMI: body mass index; SD: standard deviation
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Table 3 Summary of the studies that met the criteria of the systematic review on lifestyle interventions in overweight and obese pregnant women: non-randomised trials
Author(year)
Ethnic group/country
Participants/setting Sample size Intervention Outcome measure(s)
Conclusion
Gray-Donald etal. (2000)[38]
NativeAmericans/Canada
Recruited before the 26th week ofpregnancy, non-parallel recruitment ofcontrol and intervention arms.Mean BMI = 29.6 kg/m2 (SD = 6.45) innon-intervention arm and mean BMI =30.8 kg/m2 (SD = 6.85) in interventionarm at baseline.
219107 in non-interventionarm; 112 ininterventionarm
Dietary and weight counsellingExercise groups provided
Gestational weightgain; gestationaldiabetes;Caesarean section;birthweight;postpartum weightretention
No statistically significant difference ingestational weight gain, prevalence ofgestational diabetes, Caesarean section orlarge for gestational age baby
Olson etal. (2004)[51]
96% white/USA
Recruited before third trimester.Hospital and clinic settingBMI range: 19.8 to 29 kg/m2
498381 in non-interventionarm; 117 intheinterventionarm
Used the Institute of Medicinerecommended guidelines on weight gain;‘health book’ used to record diet andexercise and contained healthy eating andexercise information
Gestational weightgain; birthweight
No statistically significant reduction ingestational weight gain or prevalence oflarge for gestational age baby
Claessonet al.(2007)[36]
Not stated.PredominantlyCaucasian/Sweden
Obese and registered at antenatal careclinic.BMI ≥ 30 kg/m2
348193 in non-interventionarm; 155 ininterventionarm
Nutritional habits interview, weeklycounselling and aqua aerobic sessions
Gestational weightgain; Caesareansection.
Statistically significant reduction ingestational weight gain; no difference inprevalence of Caesarean section
Kinnunenet al.(2007)[37]
Over 90%Caucasian/Finland
First-time pregnant women who wereobese (BMI ≥ 30 kg/m2)
19695 in non-interventionarm; 101 ininterventionarm
Individual counselling at each antenatalvisits. Dietary guidance and optional activitysessions.
Gestational weightgain; diet change;birthweight
No statistically significant reduction ingestational weight gain or prevalence oflarge for gestational age baby. Statisticallysignificant reduction in dietary glycaemicload.
Shirazianet al.,2010 [39]
33% blacks;67% Latino/USA
Singleton obese (≥ 30 kg/m2) pregnantwomen recruited in the first trimester.Historical non-intervention group.
5428 in non-parallelcontrol arm;28 ininterventionarm)
One-to-one counselling; six structuredseminars on healthy living (healthy eatingand walking)
Gestational weightgain; gestationaldiabetes; Caesareansection
Statistically significant reduction ingestational weight gain; no difference inprevalence of gestational diabetes
Mottola etal., (2010)[35]
Not stated/Canada
Overweight (BMI ≥ 25 to 29.9 kg/m2)and obese (BMI ≥ 30 kg/m2) pregnantwomen recruited before 16 weeks’gestation; historical non-interventiongroup.
65 matchednon-parallelcontrol of 260
Individualised nutrition plan; exerciseconsisted of walking (three to four timesper week, used pedometers)
Gestational weightgain; Caesareansection; birthweight;peripartum weightretention
Possible reduction in gestational weightgain; no difference in prevalence ofCaesarean section or large for gestationalage baby; minimal effect on peripartumweight retention
BMI: body mass index; SD: standard deviation.
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The pooled RCTs included a total of 1,228 partici-pants and the pooled non-RCTs included 1,534 partici-pants. Participants were predominantly white except inthe studies by Asbee et al. [27], Gray-Donald et al. [38]and Hui et al. [33]. In the Asbee et al. study, the major-ity were described as being of Hispanic ethnicity [27].For all included RCTs, the control group received no
intervention or standard care. In the non-RCTs, mostused non-parallel controls [35,38,39,51] or controls fromanother centre [36]. The outcomes investigated in thetrials were gestational weight gain, gestational diabetes,
Caesarean section delivery, large for gestational age babyand birth weight.
Effects of the intervention on outcomesOf the 19 controlled trials, 16 measured gestationalweight gain (10 randomised, 6 non-randomised); 8recorded gestational diabetes (6 randomised, 2 non-ran-domised); 10 recorded Caesarean delivery (6 rando-mised, 4 non-randomised); 10 measured large forgestational age (6 randomised, 4 non-randomised); and7 measured birth weight (7 randomised). Meta-analyses
Table 4 Assessment of the quality of the included trials: non-randomised trials
Author (year) Populationrepresentativeness
Adequacy ofsequence generation
Masking/selection bias
Incompleteoutcome data
Contamination Samplesize
Grade ofquality
Gray-Donald et al.(2000) [38]
Yes: Registered fromclinic
No No No No: non-parallelcontrol
219 Low
Olson et al. (2004)[51]
Yes No No No No: non-parallelcontrol
560 Low
Claesson et al.(2007) [36]
Yes: Registered fromclinic
No No Yes No: selected fromnearby city
315 Low
Kinnunen et al.(2007) [37]
Yes No No No Yes 55 Low
Shirazian et al.,(2010) [39]
Yes No No Yes No: non-parallelcontrol
28 Low
Mottola et al.,(2010) [35]
Yes No No Yes No: non-parallelcontrol
65 Low
Table 5 Assessment quality of included trials: randomised trials
Author (year) Populationrepresentativeness
Adequacy ofsequence generation
Masking/selection bias
Intentionto treat
Incompleteoutcome data
Loss tofollow up
Samplesize
Grade ofquality
Polley et al. 2002[32]
Yes Yes: No Notreported
No Yes 120 Low
Hui et al. (2006)[33]
Yes: from clinic Exact method notdescribed
No Notreported
No Yes 52 Low
Wolff et al., 2008[30]
Yes Yes: computergenerated
No Notreported
Yes Yes 50 Low
Jeffries et al.,2009 [28]
Yes Yes: Opaque envelope Yes Notreported
Yes Yes 286 Low
Ong et al., 2009[42]
Yes Exact method notdescribed
No Notreported
No No 12 Low
Barakat et al.,2011 [41]
Yes Yes Yes Yes Yes Yes 160 Medium
Asbee et al.2009 [27]
Yes Yes No Notreported
Yes No 100 Low
Thornton et al.,2009 [29]
Yes Yes Yes Notreported
Yes Yes 257 Medium
Guelinckx et al.,2010 [26]
Not reported Randomised but notreported how
Not reported Notreported
Yes Notreported
99 Low
Phelan et al.,2011 [34]
Yes Yes: Opaque envelope Yes Yes Yes Yes 401 Medium,
Quinlivan et al.,2011 [59]
Yes Yes: Opaque envelope Yes Yes Yes Yes 124 Medium
Luoto et al.,2011 [43]
Yes Yes Yes Yes Yes Yes 399 Medium
Nascimento etal., 2011 [44]
Yes Yes: Opaque envelope Yes Yes Yes Yes 82 Low
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for the different outcomes are shown in Tables 6 and 7,and Figures 2, 3, 4, 5, 6, 7, 8, 9 and 10.Meta-analysis of RCTs showed that combined antena-
tal lifestyle, dietary and activity intervention restrictsgestational weight gain (Table 6 and Figure 2) and therewas a trend towards reduction in the prevalence ofgestational diabetes in overweight and obese women(Table 6 and Figure 3). However, meta-analysis of non-RCTs only showed weak evidence that lifestyle interven-tion reduces gestational weight gain (Table 7 and Figure7) and there was no evidence for a reduction in preva-lence of gestational diabetes (Table 7 and Figure 8).
There was no robust evidence that lifestyle interventionis associated with a lower prevalence of Caesarean deliv-ery or macrosomia or any alteration in birth weight(Tables 6 and 7, Figures 4,5, 6, 8, 9 and 10).
Intervention characteristicsThe nature of the interventions varied widely betweenstudies and some of the key features of the interven-tions are outlined in Tables 2 and 3. In summary, forthe six non-RCTs, three of the interventions comprisedindividual and group or seminar components[36,38,39,53], two were individual [35,52] and one was
Figure 1 Flow diagram of study selection.
Table 6 Effect estimates for randomised trials of lifestyle advice versus standard care
Outcome or subgroup Studies Participants Statistical method Effect estimate
Large for gestational age 6 1,008 Odds ratio (Fixed, 95% CI) 0.91 (0.62, 1.32)
Caesarean delivery 6 663 Odds ratio (Fixed, 95% CI) 0.96 (0.68, 1.36)
Gestational diabetes 6 1,017 Odds ratio (M-H, Fixed, 95% CI) 0.80 (0.58, 1.10)a
Gestational weight gain (kg) 10 1,228 Mean difference (Fixed, 95% CI) -2.21 (-2.86, -1.57)a
Birth weight (g) 7 1,133 Mean difference (Fixed, 95% CI) -56.64 (-120.15, 6.88)aStatistically significant pooled estimates. CI: confidence interval
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unclear [51]. Of the 13 RCTs, one comprised individualand group components [33], eight were individual[27-30,32,34] and three were group-based [26]. Wherethere were individual and group components, the latterwere usually physical activity sessions. All of the non-RCTs included dietary and physical activity guidance, asdid the majority of the randomised studies. Exceptions
were two studies which included only nutritional gui-dance [29,30] and one which included guidelines aboutweight gain and weight monitoring only [28]. Themajority of studies included dietary or physical activityguidance, with one of the non-RCTs [35] and three ofthe RCTs [29,32-34] specifying that guidance waspersonalised.
Table 7 Effect estimates for non-randomised trials of lifestyle advice versus standard care
Outcome or subgroup Studies Participants Statistical method Effect estimate
Large for gestational age 4 1,199 Odds ratio (Fixed, 95% CI) 0.85 (0.63, 1.16)
Caesarean delivery 4 1,246 Odds ratio (Fixed, 95% CI) 1.13 (0.78, 1.64)
Gestational diabetes 2 233 Odds ratio (Fixed, 95% CI) 1.51 (0.72, 3.16)
Gestational weight gain (kg) 6 1,534 Mean difference (Fixed, 95% CI) -0.42 (-1.03, 0.19)
CI: confidence interval
Study or Subgroup
Polley 2002Barakat 2009Thornton 2009Ong 2009Jeffries 2009Guelinckx 2010Phelan 2011Quinlivan 2011Luoto 2011Nascimento 2011
Total (95% CI)
Heterogeneity: Chi² = 110.98, df = 9 (P < 0.00001); I² = 92%Test for overall effect: Z = 6.69 (P < 0.00001)
Mean
13.610.9
4.9893.79.59.8
14.77
13.810.3
SD
7.24.9
6.7853.4
5.177.66.9
5.165.8
5
Total
2714
1166
25428763
21639
635
Mean
10.112.3
14.065.28.2
10.615.113.814.211.5
SD
6.23.9
7.391.3
3.026.97.5
5.235.17.4
Total
2214
1166
21439061
17941
593
Weight
3.0%3.9%
12.6%5.0%7.3%4.4%9.3%
12.6%36.4%5.5%
100.0%
IV, Fixed, 95% CI
3.50 [-0.25, 7.25]-1.40 [-4.68, 1.88]
-9.07 [-10.90, -7.25]-1.50 [-4.41, 1.41]1.30 [-1.10, 3.70]
-0.80 [-3.89, 2.29]-0.40 [-2.52, 1.72]
-6.80 [-8.63, -4.97]-0.40 [-1.48, 0.68]-1.20 [-3.96, 1.56]
-2.21 [-2.86, -1.57]
Year
2002200920092009200920102011201120112011
Experimental Control Mean Difference Mean DifferenceIV, Fixed, 95% CI
-10 -5 0 5 10Favours experimental Favours control
Figure 2 Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on gestational weight gain(kg).
Study or Subgroup
Polley 2002Wolff 2008Thornton 2009Luoto 2011Phelan 2011Quinlivan 2011
Total (95% CI)
Total eventsHeterogeneity: Chi² = 13.04, df = 5 (P = 0.02); I² = 62%Test for overall effect: Z = 1.38 (P = 0.17)
Events
20
1173114
101
Total
2723
1162168163
526
Events
13
19597
17
106
Total
2227
1161798661
491
Weight
1.2%3.7%
20.0%49.6%6.8%
18.8%
100.0%
M-H, Fixed, 95% CI
1.68 [0.14, 19.85]0.15 [0.01, 3.04]0.53 [0.24, 1.18]1.04 [0.68, 1.58]1.77 [0.65, 4.82]0.18 [0.06, 0.56]
0.80 [0.58, 1.10]
Year
200220082009201120112011
Experimental Control Odds Ratio Odds RatioM-H, Fixed, 95% CI
0.05 0.2 1 5 20Favours experimental Favours control
Figure 3 Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on risk of gestationaldiabetes.
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Study or Subgroup
Polley 2002Wolff 2008Thornton 2009Guelinckx 2010Phelan 2011Nascimento 2011
Total (95% CI)
Total eventsHeterogeneity: Chi² = 7.35, df = 5 (P = 0.20); I² = 32%Test for overall effect: Z = 0.23 (P = 0.82)
Events
22
91113325
164
Total
2723
116428139
328
Events
63
837
4229
170
Total
2227
116438641
335
Weight
9.3%3.8%
27.1%7.7%
36.6%15.4%
100.0%
M-H, Fixed, 95% CI
0.21 [0.04, 1.19]0.76 [0.12, 5.01]1.45 [0.80, 2.63]1.82 [0.63, 5.28]0.72 [0.39, 1.33]0.74 [0.29, 1.89]
0.96 [0.68, 1.36]
Year
200220082009201020112011
Experimental Control Odds Ratio Odds RatioM-H, Fixed, 95% CI
0.1 0.2 0.5 1 2 5 10Favours experimental Favours control
Figure 4 Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on risk of Caesarean delivery.
Study or Subgroup
Polley 2002Thornton 2009Guelinckx 2010Phelan 2011Luoto 2011Nascimento 2011
Total (95% CI)
Total eventsHeterogeneity: Chi² = 5.88, df = 4 (P = 0.21); I² = 32%Test for overall effect: Z = 0.51 (P = 0.61)
Events
095
14268
62
Total
27116
4281
21639
521
Events
043
14348
63
Total
22116
4386
17941
487
Weight
6.5%4.6%
19.9%57.9%11.0%
100.0%
M-H, Fixed, 95% CI
Not estimable2.36 [0.70, 7.88]1.80 [0.40, 8.07]1.07 [0.48, 2.42]0.58 [0.34, 1.02]1.06 [0.36, 3.18]
0.91 [0.62, 1.32]
Year
200220092010201120112011
Experimental Control Odds Ratio Odds RatioM-H, Fixed, 95% CI
0.2 0.5 1 2 5Favours experimental Favours control
Figure 5 Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on risk of large forgestational age baby.
Study or Subgroup
Wolff 2008Thornton 2009Guelinckx 2010Luoto 2011Quinlivan 2011Nascimento 2011Phelan 2011
Total (95% CI)
Heterogeneity: Chi² = 6.41, df = 6 (P = 0.38); I² = 6%Test for overall effect: Z = 1.75 (P = 0.08)
Mean
3,7573,5263,4923,5323,5003,2673,430
SD
617608468514556700650
Total
2311642
216633981
580
Mean
3,8953,5863,4193,6593,4003,2283,442
SD
485560425455781591629
Total
2711643
179614186
553
Weight
4.2%17.8%11.2%44.1%7.0%5.0%
10.7%
100.0%
IV, Fixed, 95% CI
-138.00 [-449.53, 173.53]-60.00 [-210.42, 90.42]73.00 [-117.18, 263.18]
-127.00 [-222.61, -31.39]100.00 [-139.29, 339.29]39.00 [-245.59, 323.59]
-12.00 [-206.19, 182.19]
-56.64 [-120.15, 6.88]
Year
2008200920102011201120112011
Experimental Control Mean Difference Mean DifferenceIV, Fixed, 95% CI
-200 -100 0 100 200Favours experimental Favours control
Figure 6 Forest plot of randomised trials investigating the effect of lifestyle advice versus standard care on birthweight.
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DiscussionSummary of main findingsAntenatal lifestyle, dietary and activity advice for over-weight and obese pregnant women restricts maternalweight gain during pregnancy and lowers the prevalenceof gestational diabetes in women who are overweight orobese. However, the quality of the study designs wasgenerally poor. The reduction in gestational weight gainwas observed to be statistically significant in the meta-analysis of randomised trials (10 RCTs; n = 1,228; -2.21
kg (95% CI, -2.86 to -1.57 kg)) but non-significant inthe meta-analysis of non-randomised trials (six non-RCTs; n = 1,534). No effects of antenatal lifestyle inter-ventions were identified in obese and overweight preg-nant women in relation to Caesarean delivery, large forgestational age, birth weight and macrosomia (> 4 kg).
InterpretationThere is evidence to suggest antenatal lifestyle interven-tions may restrict gestational weight gain and a trend
Study or Subgroup
Gray-Donald 2000Olson 2004Kinnunen 2007Mottola 2010
Total (95% CI)
Total eventsHeterogeneity: Chi² = 5.20, df = 3 (P = 0.16); I² = 42%Test for overall effect: Z = 1.02 (P = 0.31)
Events
3732
012
81
Total
1061794965
399
Events
3183
851
173
Total
10338156
260
800
Weight
23.1%49.2%8.9%
18.8%
100.0%
M-H, Fixed, 95% CI
1.25 [0.70, 2.23]0.78 [0.50, 1.23]0.06 [0.00, 1.03]0.93 [0.46, 1.86]
0.85 [0.63, 1.16]
Year
2000200420072010
Lifestyle advice Standard care Odds Ratio Odds RatioM-H, Fixed, 95% CI
0.5 0.7 1 1.5 2Favours experimental Favours control
Figure 7 Forest plot of non-randomised trials investigating the effect of lifestyle advice versus standard care on risk of large forgestational age baby.
Study or Subgroup
Gray-Donald 2000Claesson 2008Shirazian 2009Mottola 2010
Total (95% CI)
Total eventsHeterogeneity: Chi² = 1.15, df = 3 (P = 0.76); I² = 0%Test for overall effect: Z = 0.64 (P = 0.52)
Events
1535103
63
Total
1062952165
487
Events
1339
718
77
Total
10337620
260
759
Weight
21.7%57.9%7.2%
13.2%
100.0%
M-H, Fixed, 95% CI
1.14 [0.51, 2.53]1.16 [0.72, 1.89]1.69 [0.48, 5.93]0.65 [0.19, 2.28]
1.13 [0.78, 1.64]
Year
2000200820092010
Lifestyle advice Standard care Odds Ratio Odds RatioM-H, Fixed, 95% CI
0.2 0.5 1 2 5Favours experimental Favours control
Figure 8 Forest plot of non-randomised trials investigating the effect of lifestyle advice versus standard care on risk of Caesareansection.
Study or Subgroup
Gray-Donald 2000Shirazian 2009
Total (95% CI)
Total eventsHeterogeneity: Chi² = 0.01, df = 1 (P = 0.93); I² = 0%Test for overall effect: Z = 1.10 (P = 0.27)
Events
156
21
Total
9921
120
Events
104
14
Total
9320
113
Weight
74.9%25.1%
100.0%
M-H, Fixed, 95% CI
1.48 [0.63, 3.49]1.60 [0.38, 6.81]
1.51 [0.72, 3.16]
Year
20002009
Lifestyle advice Standard care Odds Ratio Odds RatioM-H, Fixed, 95% CI
0.2 0.5 1 2 5Favours experimental Favours control
Figure 9 Forest plot of non-randomised trials investigating the effect of lifestyle advice versus standard care on risk of gestationaldiabetes.
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towards a reduced prevalence of gestational diabetes, butthere was no statistical effect on other important clinicaloutcomes, possibly due to inadequate power of the com-bined sample size. The effect on restricted weight gainand gestational diabetes was not consistent across all thetrial populations and therefore cannot be generalised.There was also wide variation in the types of interven-tions evaluated in the studies. The majority were indivi-dual-based and most provided generic guidancecomprising mainly dietary and physical activity informa-tion, with few tailoring guidelines. There was consider-able heterogeneity in intervention design and no obviouspatterns between intervention type and study outcomes.For the gestational weight gain and gestational diabetesoutcomes, both the successful and non-successful studiesincluded those which were personalised, combined physi-cal activity and dietary guidance and were individual-based. Moreover, degrees of weight gain restrictionachieved were modest overall. It is even harder to makeconclusions regarding the specific behaviour change stra-tegies included (for example, monitoring and goal set-ting) or theoretical basis of interventions since these weretypically poorly reported.Identifying specific components of successful interven-
tions aids understanding of how interventions are havingan effect and clear reporting of intervention design allowsfor easier replication [54]. Previous reviews have attemptedto make conclusions regarding specific effective compo-nents of interventions. Suggestions that weight monitoringand setting weight goals could be useful [46] and also mon-itoring along with education counselling and physical activ-ity sessions [51,55] have been made. Another reviewsuggested that interventions should be based on the Theoryof Planned Behaviour, but the rationale for using thismodel over others in this population was unclear [56].None of these reviews examined intervention componentssystematically. A more recent review by Gardner et al.assessed interventions targeting gestational weight gain
from a psychological perspective and specifically examinedintervention content and delivery methods [57]. Thisreview comprised 10 controlled trials, all included in thecurrent review; only two of the studies reported basinginterventions on theory and the studies used, on average,five behaviour change strategies (self-monitoring, feedbackprovision and setting behavioural goals were the most com-mon), but no conclusions could be drawn as to their contri-bution to study outcomes. Broadly consistent with thiswere the four studies in the current review which were notincluded in the review by Gardner et al. [57]. Their reviewquestioned the evidence supporting the benefits of weightmonitoring, but tentatively suggested that information pro-vision had been underused and that it might be of benefitto have a narrower focus of intervention targets [57].
Comparison with other systematic reviews and strengthsOur study adds to a growing body of evidence that aimsto evaluate lifestyle intervention as a means to minimisethe adverse outcome associated with obesity in preg-nancy. In comparison to other published reviews[45,46,56], we have adopted an original approach bybroadening the literature source (multiple data sources,no language restriction), focusing on relevant clinicaloutcomes (such as Caesarean section, gestational dia-betes, macrosomia), and improving our sensitivity bymeta-analysing both RCTs and non-RCTs. Furthermore,to minimise bias, the review methodology was registereda priori (Prospero number CRD420111122 http://www.crd.york.ac.uk/PROSPERO). We therefore believe ourreview provides a comprehensive and reliable analysis ofthe current evidence and for the first time highlightsthat lifestyle intervention in pregnancy may reduce theprevalence of gestational diabetes.
Limitations of this systematic reviewThe evidence summarised in this work comes fromavailable studies of which most are of low quality, with
Study or Subgroup
Gray-Donald 2000Olson 2004Kinnunen 2007Claesson 2008Shirazian 2009Mottola 2010
Total (95% CI)
Heterogeneity: Chi² = 28.55, df = 4 (P < 0.00001); I² = 86%Test for overall effect: Z = 1.35 (P = 0.18)
Mean
1214.814.68.7
8.0612
SD
6.44.685.4
5.517.275.7
Total
10417948
1432165
560
Mean
13.214.114.311.3
15.420
SD
8.34.514.15.8
7.520
Total
9638156
16120
260
974
Weight
8.8%55.5%10.7%23.2%1.8%
100.0%
IV, Fixed, 95% CI
-1.20 [-3.27, 0.87]0.70 [-0.12, 1.52]0.30 [-1.57, 2.17]
-2.60 [-3.87, -1.33]-7.36 [-11.89, -2.83]
Not estimable
-0.42 [-1.03, 0.19]
Year
200020042007200820092010
Lifestyle intervention Control Mean Difference Mean DifferenceIV, Fixed, 95% CI
-4 -2 0 2 4Favours experimental Favours control
Figure 10 Forest plot of non-randomised trials investigating the effect of lifestyle advice versus standard care on gestational weightgain (kg).
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http://www.crd.york.ac.uk/PROSPEROhttp://www.crd.york.ac.uk/PROSPERO
-
only four studies fulfilling a medium quality score.Hence, the evidence base is weak and calls for morerobust studies. Our trial population is relatively small,the intensity and duration of the interventions of trialsvaried and trials were predominantly USA in origin; aphenomenon common to many public health reviews,especially on obesity. Although our focus was onantenatal lifestyle intervention for obese and overweightpregnant women, our search yielded some studies thatcontained a mixed group of obese and normal weightwomen and we excluded all the non-obese participantsfrom our analysis. Still, this may lead to inconsistenciesin measuring the effect of the intervention as well asunder- or overestimating the treatment effect. Further-more, even though our search was systematic and rigor-ous, we could have missed eligible studies inadvertently.
ConclusionsThis review reveals that lifestyle interventions for obeseand overweight women during pregnancy restrict gesta-tional weight gain and a trend was evident towardsreducing the prevalence of gestational diabetes. How-ever, the quality of the published studies is mainly poor.This then highlights a paradox. At a time when solu-tions to address adverse outcome associated with mater-nal overweight and obesity are identified as a publichealth priority, we find that most of the research evi-dence lacks robustness to inform future evidence-basedlifestyle interventions for obese pregnant women. Thereis thus a research gap regarding the effectiveness of life-style intervention in pregnancy. It is unlikely that furthermeta-analysis will help to refine the quality of evidencebecause studies demonstrated significant heterogeneityin relation to demography, outcome measurement, fol-low-up and degree of intervention. Hence, we concludethat there is the need for a well-designed large-scaleprospective trial which examines combined antenatallifestyle interventions in obese pregnant women that issuitably powered and incorporates robust methodologyin accordance with standards set by Medical ResearchCouncil’s framework for evaluating complex interven-tions [58]. There are two such studies which are cur-rently ongoing called LIMIT (ACTRN 12607000161426)and UPBEAT (ISRCTN89971375). Both of these studiesare appropriately powered to show convincingly whetherlifestyle intervention is most likely to improve pregnancyoutcome or not.
AcknowledgementsWe acknowledge Lisa Xue, Royal College of Obstetricians andGynaecologists Librarian, for her help in acquiring most of the manuscriptsin time. We also acknowledge Guy’s and St Thomas’ charity for supportingE-ON. This manuscript presents independent research commissioned by theNational Institute for Health Research (NIHR, UK) under the programmegrants for Applied Research programme RP-0407-10452. The views expressed
in this manuscript are those of the authors and not necessarily those of theNational Health Service, the NIHR or the Department of Health.
Author details1Department of Women’s Health, Guy’s and St Thomas’ NHS FoundationTrust (King’s Health Partners), St Thomas’ Hospital, Westminster Bridge Road,London, SE 1 7EH, UK. 2London School of Hygiene and Tropical Medicine,Keppel Street, London, WC1E 7HT, UK. 3School of Medicine, King’s CollegeLondon, Strand, London, WC2R 2LS, UK. 4Department of Epidemiology andPublic Health, University College London, Gower Street, London WC1E 6BT,UK.
Authors’ contributionsThe idea was conceived by PD and EO-N. The literature search and meta-analysis were by RV and EO-N and all contributed to the write up. Allauthors read and approved the final version of the manuscript.
Competing interestsThe authors declare that they have no competing interests.
Received: 23 December 2011 Accepted: 10 May 2012Published: 10 May 2012
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Pre-publication historyThe pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1741-7015/10/47/prepub
doi:10.1186/1741-7015-10-47Cite this article as: Oteng-Ntim et al.: Lifestyle interventions foroverweight and obese pregnant women to improve pregnancyoutcome: systematic review and meta-analysis. BMC Medicine 2012 10:47.
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AbstractBackgroundMethodsResultsConclusion
BackgroundMethodsEligibility criteriaInformation sourcesSearch strategyStudy selectionData collection processData itemsRisk of bias in individual studiesSummary and analysis of studies that meet the criteriaSummary measures and data synthesis
ResultsStudy characteristicsEffects of the intervention on outcomesIntervention characteristics
DiscussionSummary of main findingsInterpretationComparison with other systematic reviews and strengthsLimitations of this systematic review
ConclusionsAcknowledgementsAuthor detailsAuthors' contributionsCompeting interestsReferencesPre-publication history
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