Prev Med Rep. 2015; 2: 448–461.
Published online 2015 May 24. doi: 10.1016/j.pmedr.2015.05.009
PMCID: PMC4721374
aSchool of Psychological & Health Sciences, University of Strathclyde, Glasgow, Scotland, G1 1QE, United Kingdom
bBritish Heart Foundation Glasgow Cardiovascular Research Centre, 126 University Place, Glasgow G11 8TA, United Kingdom
A.F. Kirk: ku.ca.htarts@krik.nosilA
⁎Corresponding
author at: School of Psychological & Health Sciences, Room 532
Graham Hills Building, University of Strathclyde, 40 George Street,
Glasgow, G1 1QE, United Kingdom. Email: ku.ca.htarts@krik.nosilA
This article has been cited by other articles in PMC.
Abstract
Purpose
To
systematically review lifestyle interventions for women with prior
Gestational Diabetes Mellitus (GDM) to report study characteristics,
intervention design and study quality and explore changes in 1) diet,
physical activity and sedentary behaviour; 2) anthropometric outcomes
and; 3) glycaemic control and diabetes risk.
Methods
Databases
(Web of Science, CCRCT, EMBASE and Science DIRECT) were searched (1980
to April 2014) using keywords for controlled or pre–post design trials
of lifestyle intervention targeting women with previous GDM reporting at
least one behavioural, anthropometric or diabetes outcome. Selected
studies were narratively synthesized with anthropometric and glycaemic
outcomes synthesized using meta-analysis.
Results
Three
of 13 included studies were rated as low bias risk. Recruitment rates
were poor but study retention good. Six of 11 studies reporting on
physical activity reported favourable intervention effects. All six
studies reporting on diet reported favourable intervention effects. In
meta-analysis, significant weight-loss was attributable to one Chinese
population study (WMD = − 1.06 kg (95% CI = − 1.68, − 0.44)). Lifestyle
interventions did not change fasting blood glucose (WMD = − 0.05 mmol/L,
95% CI = − 0.21, 0.11) or type 2 diabetes risk.
Conclusions
Lack
of methodologically robust trials gives limited evidence for the
success of lifestyle interventions in women with prior GDM. Recruitment
into trials is challenging.
Keywords: Gestational diabetes, Lifestyle, Review
Introduction
Gestational
Diabetes Mellitus (GDM) is a form of diabetes that is diagnosed during
pregnancy and affects up to 16% of pregnant women (Coustan et al., 2010). Recent changes in guidelines (Coustan et al., 2010)
for clinical diagnosis of GDM, in addition to upward trends in obesity
and unhealthy lifestyles, has increased the number of women being
diagnosed (Dabelea et al., 2005). Progression to type 2 diabetes for women with GDM is reported to be between 15 and 50% at 5 years (Kim et al., 2002). Furthermore weight and BMI are significant predictors of development of type 2 diabetes at 15-year follow-up (Linne et al., 2002).
Guidelines on type 2 diabetes prevention (National Institute of Health and Care Excellence, 2008)
clearly state that high-risk populations, such as women with GDM,
should be offered lifestyle interventions. In women with GDM, physical
activity and dietary change successfully improves glycaemic control,
body composition, reduces requirements for insulin and may prevent onset
GDM in subsequent pregnancies and future development of type 2 diabetes
(Ruchat and Mottola, 2013, Bao et al., 2014).
The Diabetes Prevention Program (DPP) showed that lifestyle
interventions and Metformin reduced type 2 diabetes incidence by 58% and
31% respectively in people with impaired glucose tolerance (IGT),
including those with a history of GDM (Ratner et al., 2008). These reductions in incidence rate were maintained up to 10 years (Knowler et al., 2009).
Several studies examining the effectiveness of lifestyle interventions in women with prior GDM have recently been published (Cheung et al., 2011, Ferrara et al., 2011, McIntyre et al., 2012) and more trials are in progress (Ferrara et al., 2014, Infanti et al., 2013a, Shih et al., 2013),
however, evidence from intervention trials within the general
population of pregnant and postpartum women suggests that behaviour
change is challenging in these groups (Currie et al., 2013, Gilinsky et al., 2014/07). Similarly, research with GDM populations have reported difficulties recruiting or retaining participants (Cheung et al., 2011), and compared with women with IGT and no prior history of GDM, poorer engagement in lifestyle changes (Ratner et al., 2008).
These findings suggest that lifestyle interventions and research
methods may require adaptation for women with GDM. Lifestyle
interventions for preventing type 2 diabetes in women with prior GDM
have not been systematically reviewed to date, yet this is important to
inform future research and practice.
The
objectives of this research were to systematically review published
studies investigating lifestyle interventions for women with previous
diagnosis of GDM to explore changes in 1) behavioural outcomes (diet,
physical activity and sedentary behaviour); 2) anthropometric outcomes
and; 3) glycaemic control and diabetes risk. Study characteristics and
quality in addition to intervention content and design are also
reported.
Methods
The review was registered with PROSPERO International prospective register of systematic reviews (www.crd.york.ac.uk/PROSPERO). Methods of the review followed COCHRANE (http://www.cochrane.org) and PRISMA guidance (http://www.prisma-statement.org), which specify recommended quality criteria for conducting and reporting systematic reviews and meta-analyses.
Study selection
We
included lifestyle intervention studies targeting women with previous
diagnosis of GDM. Although recruitment and interventions could commence
during pregnancy, as the focus was on prevention of type 2 diabetes in
women with prior GDM, studies were only included if they reported
interventions and outcomes during the postpartum period. Included
interventions were those promoting weight loss or physical activity,
change in diet, or decreasing sedentary behaviour and delivered via
structured exercise programmes, lifestyle counselling, health education,
and self-management programmes. Studies had to include at least one
behavioural (diet, physical activity or sedentary behaviour)
anthropometric (weight, BMI, percent body fat, waist or hip
circumference) or diabetes outcome (measure of glycaemic control or
diabetes risk). We included randomised controlled trials (RCTs),
controlled trials or pre–post studies in the systematic review, however
only RCTs were included in meta-analysis. We included all
control/comparison groups (e.g. usual care, a waiting list, no treatment
and/or a minimal intervention (e.g. leaflet)).
Studies
not in the English language; dissertations, expert opinion,
non-published studies and conference abstracts were excluded, however we
contacted authors of relevant conference
abstracts/protocol/baseline/methods papers to identify published data.
Studies conducted with pregnant women with no diagnosis of GDM,
pre-existing or current type 1 or type 2 diabetes, or women with a
positive glucose challenge test who did not meet criteria for GDM were
also excluded. There were no exclusions based on time since GDM
diagnosis.
Studies obviously not meeting inclusion criteria were eliminated at title stage, thereafter abstracts were reviewed. Fig. 1 notes reasons for exclusion. Remaining studies were downloaded for full-text review.
Data sources and searches
The
search strategy was developed in consultation with a subject specialist
librarian. We searched the following databases: Web of Science
(inclusive of Medline), Cochrane Library: Cochrane Central Register of
Controlled Trials (CCRCT), EMBASE (on OVID), Science DIRECT from
1980–April 2014, selecting English-only abstracts. Terms used were:
(pregnancy diabetes mellitus or gestational diabetes) AND TOPIC:
(intervention* or prevent*) AND TOPIC: (“physical activity” or walking
or exercise or sedentary or sitting or diet or lifestyle) AND TOPIC:
(controlled study or trial*). Reference lists from all included papers
were searched.
Data extraction and quality assessment
One
author searched and extracted data from all studies (ASG). Two authors
(AFK & ARH) reviewed in total 50% (i.e. 25% each) of full-text
studies to check they met inclusion criteria, check correct extraction
of data and assess quality assessment indicators. A data extraction form
was developed to extract data on: study population, interventions and
comparator conditions, recruitment and retention methods and all
relevant outcomes (i.e. behavioural, anthropometric, progression to type
2 diabetes and glycaemic control). The CONSORT flow diagram was used to
extract numbers approached, randomised, allocated and receiving the
intervention/comparator conditions and numbers and reasons for
loss-to-follow-up (Moher et al., 2001). Authors were contacted if further information was required.
Methodological
quality was assessed using criteria for judging bias in intervention
studies recommended by Cochrane. All studies were coded as adequate, not
adequate, unclear or not applicable in relation to sequence generation,
allocation concealment, blinding of outcome assessors, retention at
follow-up and handling of data (criteria for coding given in Table 2). These quality indicators were then used to assign each study with an overall risk of bias rating of high, low or unclear.
Data synthesis and analysis
All extracted study characteristics and risk of bias data was entered into evidence tables (See Table 1, Table 2).
A synthesis is summarized in the results section below. After
extraction the following outcomes were synthesized using meta-analysis:
anthropometric – change in weight (available in five studies) and
glycaemic – change in fasting blood glucose (available in four studies).
Inclusion within the meta-analysis was dependent on the study being of a
randomised controlled design and data being reported within the paper
or from author contacts. We did not conduct a meta-analysis of
behavioural outcomes due to large variability in the methods of
measurement and units of measure for the behaviour.
For
the meta-analyses, we conducted random effects analysis in RevMan 5.0,
analysing the between-groups difference in each outcome at the last
follow-up point or between groups change from baseline (depending on
what was reported in the published paper) using the weighted mean
difference (WMD) measure. We present outcomes in terms of efficacy in
the short-term (e.g. 13 weeks or less follow-up), short-medium term
(i.e. 6 months follow-up), medium-term (i.e. 12 months follow-up) and
long-term (i.e. 24 months follow-up or greater). Heterogeneity was
investigated using chi-square (Q-statistic), based on observing a
p-value of < 0.05, and the I2 test, with levels > 50% suggestive
of substantial heterogeneity. We did not conduct assessment of
publication bias due to the small number of studies eligible for
inclusion in the meta-analysis.
Results
Identification of studies
A
total of 1239 citations were identified, of these 925 were excluded at
title stage and 265 at abstract stage. We assessed 28 primary studies
and 21 reviews for potentially relevant studies. We did not find any
additional citations within the reviews. Of the primary studies, 12 were
excluded due to not being conducted within a GDM population (however,
some included a limited number of women with GDM as ‘high-risk’
individuals but results could not be separated). A further three
articles were excluded due to being conducted solely in pregnancy, not
targeting weight loss/behaviour change or not reporting the results of
an intervention (see Fig. 1).
In total 13 studies were included in the systematic review (Ratner et al., 2008, Cheung et al., 2011, Ferrara et al., 2011, McIntyre et al., 2012, Cheung et al., 2007, Hu et al., 2012, Kim et al., 2012, Peterson and Jovanovic, 1995, Philis-Tsimikas et al., 2014, Reinhardt et al., 2012, Shyam et al., 2013, Shek et al., 2014, Wein et al., 1999), five in the meta-analysis of anthropometric outcomes (McIntyre et al., 2012, Hu et al., 2012, Kim et al., 2012, Reinhardt et al., 2012, Shyam et al., 2013, Shek et al., 2014, Wein et al., 1999) and four in the meta-analysis of glucose outcomes (McIntyre et al., 2012, Hu et al., 2012, Kim et al., 2012, Shyam et al., 2013).
Two eligible studies included in the review were found as a result of
the cited reference search, while all others were identified via the
database search.
Study characteristics
Table 1 summarizes study descriptors, intervention and comparator conditions, outcomes and findings.
Of the 13 studies, ten were RCTs (Ratner et al., 2008, Cheung et al., 2011, Ferrara et al., 2011, McIntyre et al., 2012, Hu et al., 2012, Kim et al., 2012, Reinhardt et al., 2012, Shyam et al., 2013, Shek et al., 2014, Wein et al., 1999). Two studies were pre–post (Cheung et al., 2007, Philis-Tsimikas et al., 2014) and one was an RCT cross-over design (Peterson and Jovanovic, 1995). All RCTs, except (Ratner et al., 2008), adopted a two-group design. Ratner et al. (Ratner et al., 2008)
reported data from women with a history of GDM from the DPP
intervention, using a three-group design (i.e. lifestyle intervention,
metformin and a drug–placebo control). Five studies took place in the US
(Ratner et al., 2008, Ferrara et al., 2011, Kim et al., 2012, Peterson and Jovanovic, 1995, Philis-Tsimikas et al., 2014), five in Australia (Cheung et al., 2011, McIntyre et al., 2012, Cheung et al., 2007, Reinhardt et al., 2012, Wein et al., 1999), one in China (Hu et al., 2012), one in Hong Kong (Shek et al., 2014) and one in Malaysia (Shyam et al., 2013).
Interventions
Three study interventions targeted physical activity only, through face-to-face counselling and follow-up phone calls (Cheung et al., 2011, McIntyre et al., 2012) or a web-based pedometer intervention (Kim et al., 2012). Two targeted diet only through through face-to-face counselling (Peterson and Jovanovic, 1995) or telephone-based education (Wein et al., 1999). Eight targeted a combination of diet and physical activity (Ratner et al., 2008, Ferrara et al., 2011, Moher et al., 2001, Cheung et al., 2007, Peterson and Jovanovic, 1995, Philis-Tsimikas et al., 2014, Reinhardt et al., 2012, Shyam et al., 2013). Three studies provided information related to intervention adherence (Kim et al., 2012, Ferrara et al., 2011, Philis-Tsimikas et al., 2014).
Comparators
Comparison conditions were metformin and a placebo drug (Ratner et al., 2008), educational information focused on conventional dietary recommendations (Shyam et al., 2013), written educational materials (Cheung et al., 2011, Ferrara et al., 2011, McIntyre et al., 2012, Hu et al., 2012, Wein et al., 1999), and usual care/no treatment (Reinhardt et al., 2012, Shek et al., 2014). Hu et al. (Hu et al., 2012)
also provided lifestyle change information via two face to face
education classes at baseline and annually via phone/mail. In Wein et
al. (Wein et al., 1999),
the intervention group received dietary intervention, however both
groups were “advised to exercise regularly” (e.g. at least 30 min, three
times per week). In Peterson et al. (Peterson and Jovanovic, 1995)
participants acted as their own comparator condition with a change in
dietary prescription (from 40% to 55% or 55% to 40% of carbohydrate
content) at the mid-point (6-weeks) of the intervention.
Recruitment
12 studies provided information on recruitment methods used (see Table 1). The majority of studies recruited participants from hospital clinic settings (Cheung et al., 2011, Ferrara et al., 2011, Kim et al., 2012, Peterson and Jovanovic, 1995, Philis-Tsimikas et al., 2014, Reinhardt et al., 2012, Shyam et al., 2013, Shek et al., 2014, Wein et al., 1999). Recruitment ranged from 7% to 28% of all GDM clinic attendees (where information available (Cheung et al., 2011, Ferrara et al., 2011, Kim et al., 2012, Reinhardt et al., 2012)). A large number of women with GDM were contacted, with rates of successful recruitment varying between 19 and 70% (Table 1). Hu et al. (Hu et al., 2012)
reported the most favourable recruitment rate using follow-up call(s)
after mailing out a study letter to clinic attendees. Poorest
recruitment was in Kim et al. (Kim et al., 2012), where participants had to sign up proactively by providing an email address (Kim et al., 2012). It took 10 months (Reinhardt et al., 2012) to recruit for a small study (< 50 participants) and between 2–4 years for studies with > 100 participants (Ferrara et al., 2011, Hu et al., 2012, Shek et al., 2014). However, most studies provided no details on length of time to recruit.
Retention
Retention rate at the last follow-up point in the included studies was generally between 80–100%(Cheung et al., 2011, Ferrara et al., 2011, McIntyre et al., 2012, Cheung et al., 2007, Hu et al., 2012, Kim et al., 2012, Reinhardt et al., 2012, Shyam et al., 2013). In two studies, the last follow-up point was at 12–13 weeks (McIntyre et al., 2012, Kim et al., 2012) and was between 6–12 months after baseline in other studies (see Table 1). Three studies reported good retention at later follow-ups (i.e. > 90%(Ratner et al., 2008; Shyam et al., 2013; Shek et al., 2014) at three years and (Wein et al., 1999)
at 51 months). Limited details were provided on reasons for loss to
follow-up or methods used to retain participants across most studies.
Two studies reported lower retention [i.e. 77% [26] and 68% at six
months and 12 weeks (Peterson and Jovanovic, 1995), respectively].
Methodological quality
Table 2 presents an assessment of risk of bias for each study. Overall, three of the 13 studies were rated as low risk of bias (Ratner et al., 2008, Ferrara et al., 2011, Kim et al., 2012),
all used blinded outcomes assessors and provided details of how the
randomization sequence was independently developed and allocation to
study groups was concealed from investigators. Three studies were rated
as high risk of bias, due to studies being non-controlled (Moher et al., 2001, Philis-Tsimikas et al., 2014) or randomization being known prior to baseline assessments (Reinhardt et al., 2012). Seven (54%) were unclear as key study indicators were not adequately described (Cheung et al., 2011, McIntyre et al., 2012, Hu et al., 2012, Peterson and Jovanovic, 1995, Shyam et al., 2013, Shek et al., 2014, Wein et al., 1999).
Changes in behavioural outcomes
Eleven studies reported changes in behavioural outcomes (Ratner et al., 2008, Cheung et al., 2011, Ferrara et al., 2011, McIntyre et al., 2012, Cheung et al., 2007, Hu et al., 2012, Kim et al., 2012, Reinhardt et al., 2012, Shyam et al., 2013, Wein et al., 1999). See Table 1 for changes in physical activity, diet and sedentary behaviour.
Physical activity
Eleven
studies reported on change in physical activity behaviour. Six studies
found significant increases in physical activity among women with prior
GDM after receiving lifestyle interventions targeting PA only (McIntyre et al., 2012), PA and diet (Ratner et al., 2008, Cheung et al., 2007, Hu et al., 2012, Philis-Tsimikas et al., 2014, Reinhardt et al., 2012). Only one of these studies was rated as low risk of bias (Ratner et al., 2008). Of the six studies reporting change, three were change from baseline to follow-up (Ratner et al., 2008, Cheung et al., 2007, Philis-Tsimikas et al., 2014) and three were compared to physical activity behaviour among controls (McIntyre et al., 2012, Hu et al., 2012, Reinhardt et al., 2012).
Sedentary time
Two studies reported on change in sedentary behaviour via self-reported sitting time (Hu et al., 2012, Reinhardt et al., 2012).
Both report significant declines relative to the control group
following lifestyle interventions, although the changes were small and
associated with large confidence intervals. Neither study was rated as
low risk of bias.
Diet
Six studies reported on change in dietary intake (Ferrara et al., 2011, Hu et al., 2012, Philis-Tsimikas et al., 2014, Reinhardt et al., 2012, Shyam et al., 2013, Wein et al., 1999). All found some positive effects on some dietary variables favouring the intervention group (Ferrara et al., 2011, Hu et al., 2012, Philis-Tsimikas et al., 2014, Reinhardt et al., 2012, Shyam et al., 2013, Wein et al., 1999) including one study rated as low risk of bias (Ferrara et al., 2011). In one study changes in dietary variables were from baseline (Philis-Tsimikas et al., 2014) and in three studies changes were relative to the control group (Ferrara et al., 2011, Hu et al., 2012, Reinhardt et al., 2012). One study found that both intensive and low-intensity (i.e. written) dietary advice resulted in modest improvements to diet (Wein et al., 1999). In one study (Shyam et al., 2013)
both groups received different dietary interventions (i.e. focusing on
low glycaemic index or conventional low-fat dietary advice) with
resultant favourable changes in dietary variables.
Changes in anthropometric outcomes
Anthropometric outcomes were reported in all 13 studies: weight in nine studies (Ratner et al., 2008, McIntyre et al., 2012, Cheung et al., 2007, Hu et al., 2012, Kim et al., 2012, Peterson and Jovanovic, 1995, Philis-Tsimikas et al., 2014, Reinhardt et al., 2012, Shyam et al., 2013); BMI in eight studies (Cheung et al., 2011, Cheung et al., 2007, Hu et al., 2012, Kim et al., 2012, Philis-Tsimikas et al., 2014, Reinhardt et al., 2012, Shyam et al., 2013, Shek et al., 2014, Wein et al., 1999); percent body fat in three studies (McIntyre et al., 2012, Hu et al., 2012, Shyam et al., 2013); waist circumference in five studies (McIntyre et al., 2012, Hu et al., 2012, Kim et al., 2012, Reinhardt et al., 2012, Shyam et al., 2013) and hip circumference in two studies (Hu et al., 2012, Kim et al., 2012). Two studies reported on proportion achieving weight loss goals (Ferrara et al., 2011, Shyam et al., 2013). Peterson et al. (Peterson and Jovanovic, 1995) and Wan Man Shek et al. (Shek et al., 2014) measured percent body fat and waist-hip ratio respectively but did not provide results.
Six
studies found a significant reduction in weight, BMI, percent body fat
and/or waist–hip ratio among participants taking part in the
intervention group (Ratner et al., 2008, Cheung et al., 2007, Hu et al., 2012, Peterson and Jovanovic, 1995, Reinhardt et al., 2012, Shyam et al., 2013). Again only one of these studies (Ratner et al., 2008) was rated as low risk of bias. Of these, three were changes from baseline (Ratner et al., 2008, Cheung et al., 2007, Peterson and Jovanovic, 1995) and three were relative to a control group (Hu et al., 2012, Reinhardt et al., 2012, Shyam et al., 2013).
Among lifestyle interventions targeting diet and physical activity/sedentary behaviour, Ratner et al. (Ratner et al., 2008)
reported average weight loss for women with a history of GDM within the
lifestyle intervention group of 5 kg at six months, however this was
not maintained until three years and therefore weight loss was poorer at
three years compared to weight loss among women with impaired glucose
tolerance without a history of GDM. Two other studies reported
favourable changes compared to controls (Hu et al., 2012, Reinhardt et al., 2012).
Seven other studies found no significant effects of lifestyle interventions on anthropometric outcomes at follow-up (Cheung et al., 2011, Ferrara et al., 2011, McIntyre et al., 2012, Kim et al., 2012, Philis-Tsimikas et al., 2014, Shek et al., 2014, Wein et al., 1999). However, Wan Man Shek et al. (Shek et al., 2014)
found the difference between the groups in reduction in weight and
percent body fat were close to significance (p = 0.06 and p = 0.05),
with heavier participants being more likely to be diagnosed with type
two diabetes at 36 months follow-up). Also Ferrara et al. (Ferrara et al., 2011)
found lifestyle intervention participants were more likely to reach
postpartum weight loss goals, but only if they had not gained excessive
gestational weight during pregnancy.
Meta-analysis of weight outcomes
Lifestyle interventions resulted in a statistically significant reduction in weight (kg) based on data from five studies (McIntyre et al., 2012, Hu et al., 2012, Kim et al., 2012, Reinhardt et al., 2012, Shyam et al., 2013), see Fig. 2 (WMD = − 1.06 kg (95% CI = − 1.68, − 0.44, p < 0.01, I = 0%). However, as shown in Fig. 2, this significant effect was attributable to the reduction at 12 months follow-up in Hu et al. (Hu et al., 2012) (i.e. − 1.19 kg, 95% CI = − 1.87, − 0.51) due to the large sample size (and therefore weighting) of this trial.
Changes in glycaemic outcomes and diabetes risk
Glycaemic control outcomes
Glycaemic outcomes were reported in nine studies (McIntyre et al., 2012, Cheung et al., 2007, Hu et al., 2012, Kim et al., 2012, Peterson and Jovanovic, 1995, Philis-Tsimikas et al., 2014, Shyam et al., 2013, Shek et al., 2014, Wein et al., 1999) including one study rated as low risk of bias (Kim et al., 2012). These were: HbA1c (Hu et al., 2012, Philis-Tsimikas et al., 2014), fasting insulin (McIntyre et al., 2012, Hu et al., 2012, Kim et al., 2012, Peterson and Jovanovic, 1995), fasting blood glucose (McIntyre et al., 2012, Cheung et al., 2007, Hu et al., 2012, Kim et al., 2012, Shyam et al., 2013, Wein et al., 1999), 2-hour blood glucose (Cheung et al., 2007, Hu et al., 2012, Kim et al., 2012, Shyam et al., 2013, Wein et al., 1999), and HOMA–IR (McIntyre et al., 2012, Hu et al., 2012, Shek et al., 2014). Four studies did not report any glycaemic outcomes (Ratner et al., 2008, Cheung et al., 2011, Ferrara et al., 2011, Reinhardt et al., 2012). Overall three studies reported a significant positive effect of lifestyle interventions on at least one glycaemic outcome (Hu et al., 2012, Shyam et al., 2013, Wein et al., 1999).
Effects reported included a reduction in 2-hour blood glucose relative
to controls among those receiving dietary interventions only (Shyam et al., 2013, Wein et al., 1999) and reduced HOMA–IR and fasting insulin relative to controls (Hu et al., 2012). In five studies, there was no effect of lifestyle interventions on glycaemic outcomes from baseline (McIntyre et al., 2012, Cheung et al., 2007, Peterson and Jovanovic, 1995) or relative to controls (McIntyre et al., 2012, Kim et al., 2012, Shek et al., 2014). In one non-controlled study there was an increase in HbA1c from baseline (Philis-Tsimikas et al., 2014).
Meta-analysis of glycaemic outcomes
Lifestyle
interventions did not result in a statistically significant reduction
in fasting blood glucose based on data from four studies (McIntyre et al., 2012, Hu et al., 2012, Kim et al., 2012, Shyam et al., 2013) (The WMD = − 0.05 mmol/L, 95% CI = − 0.21, 0.11, p = 0.54, I = 39, see Fig. 3).
Progression to type 2 diabetes
Three studies reported on progression to type 2 diabetes (Ratner et al., 2008, Shek et al., 2014, Wein et al., 1999). Findings at 36 months (Shek et al., 2014) and 51 months (Wein et al., 1999) were non-significant for rate reduction in diabetes risk. Ratner et al. (Ratner et al., 2008)
reported that lifestyle intervention was equally effective at reducing
the rate of diabetes progression in women with and without a history of
GDM. The numbers needed to treat with lifestyle intervention was higher
among GDM women compared with women without GDM. Two studies reported on
progression to normoglycemia (Cheung et al., 2011, Shyam et al., 2013). Shyam et al. (Shyam et al., 2013) reported the difference in rate was non-significant at six months (see Table 1). Cheung et al. (Cheung et al., 2011)
reported 63% returned to normoglycemia among the intervention group,
compared to 75% among controls with no significance testing reported.
Other clinical outcomes
Although
the objective of the review did not include extracting or reporting on
other clinical outcomes three studies measured changes in blood pressure
(BP) (i.e. systolic BP (Hu et al., 2012, Philis-Tsimikas et al., 2014, Shek et al., 2014), diastolic BP (Hu et al., 2012, Philis-Tsimikas et al., 2014, Shek et al., 2014)) and blood lipids (i.e. triglyceride (Hu et al., 2012, Peterson and Jovanovic, 1995, Philis-Tsimikas et al., 2014, Shek et al., 2014), serum cholesterol (Peterson and Jovanovic, 1995), HDL-cholesterol (Hu et al., 2012, Philis-Tsimikas et al., 2014, Shek et al., 2014), LDL-cholesterol (Hu et al., 2012, Philis-Tsimikas et al., 2014, Shek et al., 2014) and total cholesterol (Hu et al., 2012, Philis-Tsimikas et al., 2014)). Details of changes in these clinical outcomes following lifestyle interventions are provided in Table 1.
Discussion
The
results of this systematic review and meta-analysis suggest there is
currently limited evidence from high quality studies on the effect of
lifestyle interventions on behavioural, anthropometric and glycaemic
outcomes among women with prior GDM.
Study characteristics
Study
quality was poor with only 3 out of the 13 studies reviewed being rated
as low risk of bias. None of the studies included were conducted in
Europe. The majority of research targets both diet and physical
activity. Interventions are mostly delivered through face to face
contact. Few studies report of intervention adherence.
Recruitment
to trials within this population appears to be challenging, but trials
tend to achieve high retention rates. The majority of studies recruit
from hospital clinics and few provide any detail on length of time
required for recruitment. More research is required which explores
feasible, acceptable and effective methods of recruitment to lifestyle
interventions for this group of the population. There is tentative
evidence that recruitment and starting lifestyle intervention during
pregnancy is beneficial (Ferrara et al., 2011). However qualitative research reports the feeling among women that the early postpartum stage is “too early” for considering lifestyle change (Cheung et al., 2011, Cheung et al., 2007). Later recruitment could be targeted during annual glucose monitoring (National Institute of Health and Care Excellence, 2008).
Notably,
previous analyses have suggested that later diabetes risk is influenced
by a variety of risk factors including diagnostic glucose levels and
ethnicity with more variable results between trials for family history,
BMI and insulin use (Kim et al., 2002).
In general, intervention trials have not stratified for these risk
factors or recently introduced categories of “overt diabetes in
pregnancy” in the IADPSG and
Diabetes
mellitus in pregnancy WHO. An exception is the DPP which recruited women
with post partum IGT. It could be speculated that trials stratified to
those most at risk might be more successful in recruitment and
interventions.
Changes in behavioural outcomes
There
is minimal evidence for a change in physical activity following
lifestyle intervention in women with prior GDM, with six out of eleven
studies reporting favourable change. The majority of these studies were
rated as high or unclear risk of bias. The exception was the DPP, which
was rated as low risk of bias and reported increased physical activity
relative to the control group of 150 min of moderate–vigorous activity
at one year (Ratner et al., 2008). However, these changes were not sustained at three year follow up (Ratner et al., 2008).
It is worth highlighting that DPP recruited women with prior GDM on
average 12 years since delivery, which may not be generalizable to a
population of women with prior GDM who are recruited for lifestyle
intervention at early stages (i.e. during pregnancy and/or within the
first few years following delivery).
Findings on change
in physical activity from this review need to be interpreted with some
caution as all studies measured change in self-reported physical
activity and sedentary behaviour. There is evidence that self-report
measures can lead to under and overestimation of participation in
physical activity (Long et al., 2013).
Future research should incorporate objective methods (i.e.
accelerometers) of measuring physical activity and sedentary behaviour.
In addition few include sedentary behaviour in their interventions (Ferrara et al., 2014, Infanti et al., 2013a, Shih et al., 2013).
This is important as sedentary behaviour is increasingly recognized as
an important target for improving cardio metabolic indicators of type 2
diabetes (Henson et al., 2013).
There
was somewhat stronger evidence regarding change to dietary variables.
One high-quality study found a reduction in percentage calories from fat
among women engaged in an adapted version of the DPP intervention (Ferrara et al., 2011). However, timing of recruitment may be important. Evidence from this review and other studies (Infanti et al., 2013b)
suggests women who successfully adopt lifestyle changes during
pregnancy may be more likely to return for preventative support (Infanti et al., 2013b) and be more successful at maintaining dietary change postpartum (Ferrara et al., 2011).
A number of studies in this review measured lifestyle intervention
effects on dietary change; those not recruiting during pregnancy were
also favourable, though these were of low quality or in unique
populations (Philis-Tsimikas et al., 2014, Reinhardt et al., 2012, Shyam et al., 2013, Wein et al., 1999).
Therefore, evidence for a positive impact of lifestyle interventions in
women with prior GDM on dietary variables postpartum remains tentative.
Future
research should also give consideration to the wider socio-economic,
social and cultural environment in which women with prior GDM live, for
example, there is evidence that inclusion of partners is important for
changing physical activity and dietary behaviours among women with young
children (Fjeldsoe et al., 2010 May, Miller et al., 2002) and is desired by women with prior GDM (Dasgupta et al., 2013).
Changes in anthropometric outcomes
There
was limited evidence in this review for significant changes in
anthropometric outcomes following lifestyle interventions among women
with prior GDM. Although the meta-analyses for weight and BMI were
statistically significant, the magnitude of change would not be
considered clinically significant (National Institute of Health and Excellence, 2010); furthermore, one trial of unclear quality, conducted in a Chinese population (Hu et al., 2012) was responsible for the small effect size found. The exception to this was in the DPP study (Ratner et al., 2008)
which found significant weight loss in the first year following
intensive lifestyle intervention among women with prior GDM, however
this was not maintained at later stages and the population may not be
generalizable, as discussed previously. Another high quality study found
that an adapted DPP intervention promoted weight loss at 12 months, but
only among women who successfully avoided excessive gestational weight
gain during pregnancy and who received intensive lifestyle intervention
immediately following GDM diagnosis (Ferrara et al., 2011).
It may be that women who more successfully adopt lifestyle changes
during pregnancy feel more motivated, self-efficacious and supported,
helping them to maintain behavioural changes into postpartum.
Results
from the DPP trial have shown maintained weight loss to be the main
predictor of risk reduction in type 2 diabetes prevention in the general
population with IGT (Knowler et al., 2009).
Therefore, it seems pertinent to focus on developing and testing
lifestyle interventions that can produce successful long-term weight
reduction among women with prior GDM. The present review found no
high-quality studies reporting favourable long-term weight outcomes in
this group, other than the subset of women from the DPP (Ratner et al., 2008).
In the general obese population long-term (≥ 12 months) weight loss has
been shown following behavioural interventions focusing on both diet
and physical activity change (Dombrowski et al., n.d.).
Weight-loss medication improved the magnitude of weight reduction. On
the one hand, among postpartum populations, dietary change alone is
considered as effective for weight-loss as dietary change in combination
with physical activity (Amorim Adegboye and Linne, 2013).
On the other hand, physical activity and sedentary behaviour change are
important, particularly as women with prior GDM are at high future high
risk of cardiovascular disease (Carr et al., 2006).
Physical activity is considered the most important modifiable risk
factor for preventing cardiovascular disease among healthy young women (Brown et al., 2014),
independent of other risk factors, including BMI. This review showed
that fewer studies focused on physical activity or sedentary behaviour,
compared with dietary change. This may reflect preferences among women
with prior GDM regarding how, when and what lifestyle changes are
adopted or a greater emphasis on dietary change in interventions
targeting women with GDM.
Changes in glycaemic outcomes and diabetes risk
Trials
among women with prior GDM, not including the DPP, showed no robust
evidence for change in glycaemic indicators or diabetes risk reduction,
despite these being important health outcomes. However, with a few
exceptions, trials did not appear to have been adequately powered or
include long enough follow-ups to demonstrate change in diabetes risk
reduction.
Summary
There is consensus that prevention of type 2 diabetes should be prioritized through lifestyle interventions (National Institute of Health and Care Excellence, 2008, Buchanan et al., 2012, England et al., 2009).
The recent diagnostic criteria for classification of GDM proposed by
the International Association of Diabetes in Pregnancy Study Group
(IADPSG) (Coustan et al., 2010)
offers opportunity for early lifestyle intervention and future
prevention of Type 2 diabetes and other disease over the lifespan. This
review shows that we currently lack an evidence base from
methodologically robust trials for how to effectively promote lifestyle
change among women with prior GDM. There is evidence quality of
methodology is improving with future study protocols providing more
detailed information and being methodologically more robust (Ferrara et al., 2014, Infanti et al., 2013a, Shih et al., 2013, Berry et al., OCT 10 2013).
Recruitment to trials and adopting lifestyle changes appear challenging
in this group. Further research is urgently required to explore
feasible, acceptable and effective lifestyle interventions for this
target group of the population.
Author contribution
A.S.G.
contributed to conception and design of the study, led on data
analysis, wrote the initial draft of the paper and reviewed the final
draft. A.F.K. initiated the conception and design of the study, assisted
in researching the data, reviewed initial drafts of the paper and
completed the final submitted paper. A.R.H. made a substantial
contribution to conception and design of the study, assisted in
researching the data and reviewed initial and final drafts of the paper.
R.S.L. contributed to conception and design of the study and reviewed
initial and final drafts of the paper.
Conflict of interest
None of the authors of this paper report a conflict of interest in relation to the material covered in this paper.
Acknowledgments
This manuscript was funded by an internal grant from the University of Strathclyde.
Footnotes
☆The work conducted in relation to this review was funded by internal funding from the University of Strathclyde.
References
- Amorim Adegboye A.R., Linne Y.M. Diet or exercise, or both, for weight reduction in women after childbirth. Cochrane Database Syst. Rev. 2013;23(7) CD005627. [PubMed]
- Bao W., Tobias D.K., Bowers K., Chavarro J., Vaag A., Grunnet L.G. Physical activity and sedentary behaviors associated with risk of progression from gestational diabetes mellitus to type 2 diabetes mellitus: a prospective cohort study. JAMA Intern. Med. 2014;174(7):1047–1055. [PubMed]
- Berry D.C., Neal M., Hall E.G., Schwartz T.A., Verbiest S., Bonuck K. Rationale, design, and methodology for the optimizing outcomes in women with gestational diabetes mellitus and their infants study. BMC Pregnancy Childbirth. OCT 10 2013;13:184. 2013. [PubMed]
- Brown W.J., Pavey T., Bauman A.E. Comparing population attributable risks for heart disease across the adult lifespan in women. Br. J. Sports Med. 2014;08 [PubMed]
- Buchanan T.A., Xiang A.H., Page K.A. Gestational diabetes mellitus: risks and management during and after pregnancy. Nat. Rev. Endocrinol. 2012;8(11):639–649. [PubMed]
- Carr D.B., Utzschneider K.M., Hull R.L., Tong J., Wallace T.M., Kodama K. Gestational diabetes mellitus increases the risk of cardiovascular disease in women with a family history of type 2 diabetes. Diabetes Care. 2006;29(9):2078–2083. [PubMed]
- Cheung N.W., Smith B.J., Henriksen H., Tapsell L.C., Bauman A. A group based healthy lifestyle program for women with previous gestational diabetes. Diabetes Res. Clin. Pract. 2007;77:333–334. [PubMed]
- Cheung N.W., Smith B.J., van der Ploeg H.P., Cinnadaio N., Bauman A. A pilot structured behavioural intervention trial to increase physical activity among women with recent gestational diabetes. Diabetes Res. Clin. Pract. 2011;92(1):E27–E29. [PubMed]
- Coustan D.R., Lowe L.P., Metzger B.E., Dyer A.R. International Association of Diabetes and Pregnancy Study Groups. The hyperglycemia and adverse pregnancy outcome (HAPO) study: paving the way for new diagnostic criteria for gestational diabetes mellitus. Am. J. Obstet. Gynecol. 2010;202(6):654. e1-6. [PubMed]
- Currie S., Sinclair M., Murphy M.H., Madden E., Dunwoody L., Liddle D. Reducing the decline in physical activity during pregnancy: a systematic review of behaviour change interventions. PLoS ONE. 2013;8(6) e66385. [PMC free article] [PubMed]
- Dabelea D., Snell-Bergeon J.K., Hartsfield C.L., Bischoff K.J., Hamman R.F., McDuffie R.S. Increasing prevalence of gestational diabetes mellitus (GDM) over time and by birth cohort: Kaiser Permanente of Colorado GDM screening program. Diabetes Care. 2005;28(3):579–584. [PubMed]
- Dasgupta K., Da Costa D., Pillay S., De Civita M., Gougeon R., Leong A. Strategies to optimize participation in diabetes prevention programs following gestational diabetes: a focus group study. PLoS ONE. 2013;8(7) e67878. [PMC free article] [PubMed]
- Dombrowski SU, Knittle K, Avenell A, Araújo-Soares V, Sniehotta FF. Long term maintenance of weight loss with non-surgical interventions in obese adults: systematic review and meta-analyses of randomised controlled trials. BMJ;348. [PMC free article] [PubMed]
- England L.J., Dietz P.M., Njoroge T., Callaghan W.M., Bruce C., Buus R.M. Preventing type 2 diabetes: public health implications for women with a history of gestational diabetes mellitus. Obstet. Gynecol. 2009;200(4):365. e1. [PubMed]
- Ferrara A., Hedderson M.M., Albright C.L., Ehrlich S.F., Quesenberry C.P., Jr., Peng T. A pregnancy and postpartum lifestyle intervention in women with gestational diabetes mellitus reduces diabetes risk factors: a feasibility randomized control trial. Diabetes Care. 2011;34(7):1519–1525. [PubMed]
- Ferrara A., Hedderson M., Albright C., Brown S., Ehrlich S., Caan B. A pragmatic cluster randomized clinical trial of diabetes prevention strategies for women with gestational diabetes: design and rationale of the gestational diabetes' effects on moms (GEM) study. BMC Pregnancy Childbirth. 2014;14(1):21. [PubMed]
- Fjeldsoe B.S., Miller Y.D., Marshall A.L. MobileMums: a randomized controlled trial of an SMS-based physical activity intervention. Ann. Behav. Med. 2010 May;39(2):101–111. [PubMed]
- Gilinsky A.S., Dale H., Robinson C., Hughes A.R., McInnes R., Lavallee D. Efficacy of physical activity interventions in post-natal populations: systematic review, meta-analysis and content coding of behaviour change techniques. Health Psychol. Rev. 2014/07;2014(03/06):1–20. [PubMed]
- Henson J., Yates T., Biddle S.J., Edwardson C.L., Khunti K., Wilmot E.G., Gray L.J., Gorely T., Nimmo M.A., Davies M.J. Associations of objectively measured sedentary behaviour and physical activity with markers of cardiometabolic health. Diabetologia. 2013;56(5):1012–1020. [PubMed]
- Hu G., Tian H., Zhang F., Liu H., Zhang S., Liu G. Tianjin gestational diabetes mellitus prevention program: study design, methods, and 1-year interim report on the feasibility of lifestyle intervention program. Diabetes. 2012;61:A39. [PubMed]
- Infanti J.J., Dunne F.P., O'Dea A., Gillespie P., Gibson I., Glynn L.G. An evaluation of Croi. My Action community lifestyle modification programme compared to standard care to reduce progression to diabetes/pre-diabetes in women with prior gestational diabetes mellitus (GDM): study protocol for a randomised controlled trial. Trials. 2013;14:121. [PubMed]
- Infanti J.J., O'Dea A., Gillespie P., O'Neill C., Glynn L.G., McGuire B.E. Barriers to participation in a community-based lifestyle intervention programme to prevent type 2 diabetes following gestational diabetes mellitus. Diabetes. 2013;62:A206.
- Kim C., Newton K.M., Knopp R.H. Gestational diabetes and the incidence of type 2 diabetes: a systematic review. Diabetes Care. 2002;25(10):1862–1868. [PubMed]
- Kim C., Draska M., Hess M.L., Wilson E.J., Richardson C.R. A web-based pedometer programme in women with a recent history of gestational diabetes. Diabet. Med. 2012;29(2):278–283. [PubMed]
- Knowler W.C., Fowler S.E., Hamman R.F., Christophi C.A., Hoffman H.J., Brenneman A.T. 10-year follow-up of diabetes incidence and weight loss in the diabetes prevention program outcomes study. Lancet. 2009;374(9702):1677–1686. [PubMed]
- Linne Y., Barkeling B., Rossner S. Natural course of gestational diabetes mellitus: long term follow up of women in the SPAWN study. BJOG Int. J. Obstet. Gynaecol. 2002;109(11):1227–1231. [PubMed]
- Long G., Brage S., Wareham N., van Sluijs E., Sutton S., Griffin S. Socio-demographic and behavioural correlates of physical activity perception in individuals with recently diagnosed diabetes: results from a cross-sectional study. BMC Public Health. 2013;13(1):678. [PubMed]
- McIntyre H.D., Peacock A., Miller Y.D., Koh D., Marshall A.L. Pilot study of an individualised early postpartum intervention to increase physical activity in women with previous gestational diabetes. Int. J. Endocrinol. 2012;2012:892019. [PubMed]
- Miller Y.D., Trost S.G., Brown W.J. Mediators of physical activity behavior change among women with young children. Am. J. Prev. Med. 2002;23(2 Suppl):98–103. [PubMed]
- Moher D., Schulz K.F., Altman D.G. The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials. Lancet. 2001;357:1191–1194. [PubMed]
- National Institute of Health and Care Excellence . Report No.: NICE Guidelines [CG63] National Institute of Health and Care Excellence; 2008. Diabetes in pregnancy: management of diabetes and its complications from pre-conception to the postnatal period.
- National Institute of Health, Excellence Care. Report No.: NICE Public Health Guidance 27. National Institute of Health and Care Excellence; 2010. Weight management before, during and after pregnancy.
- Peterson C.M., Jovanovic P.L. Randomized crossover study of 40-percent vs 55-percent carbohydrate weight-loss strategies in women with previous gestational diabetes-mellitus and nondiabetic women of 130–200-percent ideal body-weight. J. Am. Coll. Nutr. 1995;14(4):369–375. [PubMed]
- Philis-Tsimikas A., Fortmann A.L., Dharkar-Surber S., Euyoque J.A., Ruiz M., Schultz J. Dulce mothers: an intervention to reduce diabetes and cardiovascular risk in Latinas after gestational diabetes. Transl. Behav. Med. 2014;4(1):18–25. [PubMed]
- Ratner R.E., Christophi C.A., Metzger B.E., Dabelea D., Bennett P.H., Pi-Sunyer X. Prevention of diabetes in women with a history of gestational diabetes: effects of metformin and lifestyle interventions. J. Clin. Endocrinol. Metab. 2008;93(12):4774–4779. [PubMed]
- Reinhardt J.A., van der Ploeg H.P., Grzegrzulka R., Timperley J.G. Implementing lifestyle change through phone-based motivational interviewing in rural-based women with previous gestational diabetes mellitus. Health Promot. J. Austr. 2012;23(1):5–9. [PubMed]
- Ruchat S., Mottola M.F. The important role of physical activity in the prevention and management of gestational diabetes mellitus. Diabetes Metab. Res. 2013;29(5):334–346. [PubMed]
- Shek N.W., Ngai C.S., Lee C.P., Chan J.Y., Lao T.T. Lifestyle modifications in the development of diabetes mellitus and metabolic syndrome in Chinese women who had gestational diabetes mellitus: a randomized interventional trial. Arch. Gynecol. Obstet. 2014;289(2):319–327. [PubMed]
- Shih S.T.F., Davis-Lameloise N., Janus E.D., Wildey C., Versace V.L., Hagger V. Mothers after gestational diabetes in Australia diabetes prevention program (MAGDA-DPP) post-natal intervention: study protocol for a randomized controlled trial. Trials. 2013;14:339. [PubMed]
- Shyam S., Arshad F., Ghani R.A., Wahab N.A., Safii N.S., Nisak M.Y.B. Low glycaemic index diets improve glucose tolerance and body weight in women with previous history of gestational diabetes: a six months randomized trial. Nutr. J. 2013;12:68. [PubMed]
- Wein P., Beischer N., Harris C., Permezel M. A trial of simple versus intensified dietary modification for prevention of progression to diabetes mellitus in women with impaired glucose tolerance. Aust. N. Z. J. Obstet. Gynaecol. 1999;39(2):162–166. [PubMed]
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