Abstract
Although exercise during pregnancy is safe
for the mother and child. The majority of research has focused on continuous
and aerobic-focused activities, such as calisthenics, yoga and aerobic
exercise, such as swimming, jogging and dancing. Thus, obstetric and health guidelines
from many countries, such as the American College of Obstetricians and
Gynecologists (ACOG), the US Department of Health and Human Services Physical
Activity Guidelines for Americans and the World Health
Organization (WHO) state that pregnant and postpartum women should do 150 minutes of moderate-intensity aerobic activity per
week. These guidelines also list resistance exercises, such as using
weights and elastic bands, as examples of exercises. However, less direction
and guidance are provided related to resistance or strength training during
pregnancy. Thus, there is a disconnect between
the evidence related to exercise types during pregnancy and the benefits for
the mother, placenta and the offspring. Therefore, this is the first narrative
review to summarize the current state of literature focused on the influence of
gestational exercise types (aerobic, resistance/strength,
combination/concurrent, light/yoga/Pilates) on maternal, placental and
offspring responses at the gross and cellular levels.
Keywords: Pregnancy, Mother, Child,
Placental, Fetal development, Aerobic exercise
Abbreviations: ACOG: American College of
Obstetricians and Gynecologists; WHO: World Health Organization LDL-C: Low-Density
Lipoprotein Cholesterol; HDL-C: High-Density Lipoprotein Cholesterol; CRP: C-Reactive
Protein; CMR: Cardiometabolic Risk; MVPA: Moderate-To-Vigorous Physical
Activity; ROS: Reactive Oxygen Species; HIIT: High-Intensity Interval
Training; PW: Placental Weight
1. Introduction
Exercise during pregnancy initially started
with ensuring it was safe for the mother and child. Initial activities assessed
for safety included calisthenics, yoga and aerobic exercise, such as swimming,
jogging and dancing1,2 (ref). Thus, initial recommendations from
the American College of Obstetricians and Gynecologists in 1985 were restrictive,
limiting maternal heart rate to below 140 bpm, limiting strenuous activity to
only 15 minutes and focused on women who were already active, while discouraging
sedentary women from starting a new program during pregnancy3. Since the 1985 ACOG guidelines until now, substantial evidence
supports not only the safety, but also the benefit of exercise throughout
gestation for the mother, placenta and fetal development. Although a 2024
review denotes the safety of resistance training during pregnancy4, the updated ACOG guidelines from 20205 and the
2018 update of the US Department of Health and Human Services Physical Activity
Guidelines for Americans6, state that women should do “at least 150 minutes of moderate intensity aerobic activity
per week during pregnancy and the postpartum period5”. It
also states that “women who habitually engage in
vigorous-intensity aerobic activity or who were physically active before
pregnancy can continue these activities during pregnancy and the postpartum
period5”. Importantly, it lists resistance exercises,
such as using weights and elastic bands, as an example of exercises with
extensive research. However, it also states, “There
are few maternal medical conditions in which aerobic exercise is absolutely
contraindicated. When questions exist regarding the safety of aerobic exercise
in pregnancy, consultation with relevant specialists and subspecialists is
required6.” Thus, it seems there is
still a disconnect between the evidence related to exercise types during
pregnancy and the benefits for the mother, placenta and the offspring.
Therefore, this narrative review aims to summarize the current state of
literature focused on the influence of gestational exercise types (aerobic,
resistance/strength, combination/concurrent, light/yoga/Pilates) on maternal, placental
and offspring responses at the gross and cellular levels.
1.1. Prenatal Exercise Types and Maternal Health Parameters
Pregnant individuals are advised to complete at least 150
minutes of moderate-intensity exercise each week. Activities that increase
heart rate and induce mild to moderate sweating, such as walking, swimming,
stationary cycling and low-impact aerobics, are ideal. Muscle-strengthening
activities, including resistance exercises, weight training and yoga, are also
encouraged7,8. Numerous studies support the safety and
benefits of physical activity and exercise in pregnancy for gestational
individuals. This includes reduced risk of excessive gestational weight gain
and multiple adverse pregnancy conditions (i.e., gestational diabetes,
hypertensive disorders and preterm birth)9,10. Exercise during pregnancy may promote a more favorable gestational
(parent) environment through modifying parameters that influence
cardiometabolic health, such as body weight and composition11, blood lipid profiles12,13 and
inflammatory biomarkers14,15. Considering the individual physiological
benefits that accompany regular aerobic and/or resistance exercise in
non-pregnant adults, the exercise benefits for gravid individuals may differ,
depending on exercise modality or type. This section will provide an overview of
research related to the effects of aerobic, resistance or combination (aerobic
+ resistance) exercise during pregnancy on the gestational parent’s body
composition and blood parameters (i.e., lipids, inflammation, metabolome and
proteome), with a particular focus on the comparison of the exercise types.
1.2. Exercise Type
and Body Composition
In non-gravid individuals, chronic exercise has profound
effects on body composition, including changes to fat mass, lean mass and bone
mineral density. Research consistently demonstrates that the adaptations are
contingent on the magnitude and type of exercise performed. Aerobic exercise
has been shown to reduce total fat mass and body fat percent16; have minimal or no effects on lean mass17; and result in moderate improvements to bone mineral density,
particularly in the lumbar spine with load-bearing activity18. Resistance exercise alone demonstrates substantial increases in lean
mass, even under caloric restrictions19,20 and bone
mineral density21. Although reductions in fat mass with
resistance training are typically smaller, it can elicit decreases in body fat
percentage when compared with non-exercising populations17. Finally, combination exercise appears to provide the most comprehensive
benefits for body composition. This exercise type results in reduced fat mass
and increased lean mass, similar to that of aerobic or resistance exercise
alone, respectively17. Systematic reviews support the significant
effect of combination exercise for optimizing overall body composition,
highlighting additive or synergistic effects on both adipose and lean tissues
compared with single-modality intervention programs; resistance components
within these protocols help attenuate declines in bone mineral density that may
accompany aerobic exercise or weight loss alone19,21.
Pregnancy involves dramatic shifts in body composition
throughout gestation in response to and to elicit changes in fetal development.
These adaptations include increased blood volume as well as changes in the
gestational parent adipose and musculoskeletal tissues. However, weight gain above the
appropriate limit can lead to health complications for both the gravid
individual and the fetus, such as hypertension, gestational diabetes, preterm
birth, low birth weight and large-for-gestational-age infants22. Importantly,
gestational exercise may influence how fat mass, lean mass and bone mineral
density change across gestation for the gravid individual and fetus, aiding in
appropriate weight gain. Although research is more limited in pregnant
individuals, studies have been conducted to examine the associations between
gestational physical activity and body composition outcomes.
Aerobic exercise and general physical activity during pregnancy
have been associated with changes in fat mass and body fat percent.
Observational studies indicate that pregnant individuals who maintain a higher
volume of aerobic activity or greater daily step count gain less fat mass and
exhibit lower visceral adipose tissue relative to less active individuals23. Although randomized trials of structured aerobic exercise, such as
supervised walking or cycling programs, have shown only modest effects on total
fat mass relative to standard care24, habitual daily
activity appears to correlate with more favorable fat accumulation patterns25,26. It’s
been reported that pregnant individuals with overweight or obesity have reduced
excessive gestational weight gain and an attenuation of adipose tissue
accumulation with antenatal aerobic exercise relative to controls27. Similarly, structured prenatal exercise programs have
been associated with lower fat storage and improved body composition trends in pregnant
individuals relative to inactive controls28.
Collectively, these findings support aerobic activity during pregnancy, aiding
in limiting excess adipose tissue gain.
Research examining structured resistance training during
pregnancy, regardless of intensity, is limited. Light-to-moderate intensity
resistance exercise may help preserve lean mass and fat-free mass23. Observational research indicates that maintaining muscular fitness
activities may reduce muscle tissue loss, which can occur in the third
trimester as adipose tissue accumulation increases29. Long-term follow-up studies further support that prenatal exercise
exposure may influence body composition trajectories beyond pregnancy, with
associations observed up to one-year postpartum30. Despite the effect of resistance training on body composition for
non-gravid individuals and the existing literature supporting favorable
outcomes for pregnant individuals, there is a lack of large-scale randomized
trials isolating resistance training in pregnancy. Fully elucidating the
effects of resistance training alone during pregnancy on the body composition
of the gestational parent is imperative, as it has the potential to add a
protective effect for both the pregnant individual and the developing fetus.
Similarly, research on the effect of combination exercise
in pregnancy is sparse. Multi-component programs during gestation offer
balanced benefits, including lower fat-mass gains and preserved lean mass
compared to non-exercisers23,27. Considering the effects in non-gravid
adults, utilizing a combination (aerobic + resistance) exercise approach may
optimize tissue-specific outcomes, resulting in lower fat-mass and body fat
percent, while maintaining or increasing lean mass without negatively impacting
parental and fetal health.
Exercise may also influence bone
mineral density during pregnancy. Normal gestation involves calcium
mobilization to support fetal skeletal growth, often resulting in declines in
BMD of the pregnant individual31,32.
Observational studies indicate that adults who maintain higher habitual
physical activity experience smaller reductions in BMD between early and late
pregnancy compared with sedentary individuals, suggesting a protective effect
of exercise32. Direct measurement of bone changes
during pregnancy via DXA is limited due to safety concerns. However, indirect
evidence (collected via activity tracking and postpartum assessments) supports
the potential for physical activity, including aerobic, resistance or
combination types, to attenuate pregnancy-related bone loss.
1.3. Exercise Type
and Blood Lipids
For non-gravid individuals, regular exercise can
significantly impact blood lipid profiles, thus reducing cardiovascular disease
risk. These benefits include reduced Total Cholesterol (TC), Low-Density
Lipoprotein Cholesterol (LDL-C) and triglyceride levels with increased High-Density
Lipoprotein Cholesterol (HDL-C)12,13.
Moreover, it promotes a shift toward larger, less dense LDL and HDL particles,
which are less likely to contribute to atherosclerosis33. By enhancing the body’s ability to use fat as a fuel source, exercise
further improves overall lipid balance34,35.
Although research regarding differences in exercise type
in pregnancy is limited, exercise in general has been shown to improve lipid
profiles, thus supporting better cardiometabolic health. Similar to non-gravid
populations, exercise during pregnancy can result in reduced TC and LDL-C
levels, which naturally rise during pregnancy to support fetal development36,37. At the same time, physical activity can increase HDL-C,
providing further protective cardiovascular benefits. While triglyceride levels
also increase during pregnancy to supply energy for the developing fetus,
exercise can help moderate excessive increases, keeping them within a healthy
range38-40. Additionally, regular physical activity
improves lipid metabolism, enhancing the body’s ability to utilize lipids for
energy and reducing the risk of lipid-related complications, such as
gestational hyperlipidemia36,41-43.
Pregnant individuals need to maintain a healthy body
composition and metabolic profile through balanced nutrition and regular
physical activity to optimize fetal development and reduce the risk of adverse
outcomes in offspring. By managing lipid profiles and overall metabolic health,
gestational parents can significantly improve their children’s long-term health
and well-being.
1.4. Exercise Type
and Inflammation
Exercise during pregnancy may promote a more favorable
gestational environment, in part, by controlling inflammatory levels14,15. This is evidenced by reduced pro-inflammatory (e.g.,
tumor necrosis factor alpha (TNF-α), C-Reactive Protein (CRP), Interleukin 1B
(IL-1B)) and increased anti-inflammatory markers (e.g., IL-10)41,44-47. Interestingly, in non-gravid individuals
with and without chronic disease, some evidence suggests the magnitude of the
exercise effects on these biomarkers may differ between exercise types48,49. Yet, to our knowledge, there has not been a direct
comparison of exercise type during pregnancy on inflammatory markers in the
gestational environment.
Interventions using self-reported
(questionnaires) or objectively-measured (pedometers, accelerometers) physical
activity reported lower CRP46,47,50. For
example, pregnant individuals who achieved at least 11,000 steps per day had
lower CRP at 28-30 weeks’ gestation46. Another study found
that pregnant individuals who continued load-bearing endurance exercises across
pregnancy experienced lower TNF- α and leptin in late pregnancy relative to
non-exercisers and exercisers who discontinued their activity during pregnancy45. This included completing at least 40-minutes of moderate intensity
load-bearing exercise on at least 4 days per week45. Collectively, these data suggest aerobic-based physical activities or
exercises help reduce pro-inflammatory markers, especially if they are
continued across gestation.
A recent systematic review on exercise
interventions done at a moderate-to-vigorous intensity reported that concurrent
or combination exercise had a particularly positive effect on pregnant
individuals’ inflammatory markers14. Acosta-Manzano and
colleagues explored this relationship by having participants complete two sessions
per week of resistance circuits, alternating with cardiovascular blocks and one
session per week dedicated to aerobic training. All sessions were 60 minutes,
including warm-up and cool-down periods44. Exercisers
experienced reduced TNF- α in late pregnancy and lower IL-1β with increased IL-10
at delivery compared to the non-exercise group44. A later analysis found that those pregnant exercisers who increased
IL-8 also had more favorable lipid levels, as evidenced by lower TC and LDL-C
gains41. Although IL-1B, IL-6, nor TNF- α were identified as
having a mediatory effect on metabolism, it was proposed that these
pro-inflammatory markers may instead have an indirect role in other processes
related to gestational health41.
The effect of resistance training alone on
gravid individuals’ inflammatory markers is largely unstudied15. For non-gravid individuals, a recent meta-analysis reported resistance
exercise to reduce CRP, but found no significant pooled effect for TNF- α or IL-649. Considering the positive effects of resistance training on reducing
body fat in non-gravid individuals51 and the link between
adipose tissue signaling for systemic inflammation, it’s important to further
define the relationship between resistance exercise and inflammation,
particularly for pregnant individuals.
Lastly, it is worth highlighting that
physical inactivity has been associated with a less favorable gestational
environment for cardiometabolic + pro-inflammatory biomarkers based on
composite Z-scores52. In mid- and late-pregnancy, sedentary time
was associated with lower IL-6 and higher IL-10, TNF- α and leptin levels53. Taken together, the data highlight the importance of regular physical
activity across gestation to support an improved gestational environment.
Although shifts in inflammation are important
to support a healthy pregnancy54, prolonged,
excessive inflammation has been linked with adverse pregnancy outcomes (e.g.,
gestational diabetes, preeclampsia)55-57. Thus,
determining the best method for controlling pregnancy inflammation is
important. The existing literature supports that exercise during gestation is
safe, regardless of type and may be beneficial for gestational parent
inflammation. Although some results conflict, this could partially be due to
differences in the exercise mode across studies, as well as other
methodological differences, making it difficult to draw comparisons. More
research is needed to better define the relationship between exercise type and
pro- and anti-inflammatory markers during gestation. Defining the key
differences between exercise types may have a significant role in creating
better, individual-based exercise prescriptions for pregnant individuals,
resulting in the greatest benefits.
1.5. Exercise Type and Omics: Metabolomic and
Proteomic Highlights
Omics analyses have been used to identify and
characterize molecular differences in biological systems, allowing the field to
better characterize the extensive effects of physical activity and exercise. While
there are various types of omics analyses utilized in understanding the
biological differences during pregnancy58, metabolomic and
proteomic approaches explore more downstream outcomes of molecular changes. The
metabolome and proteome can be assessed by utilizing high-throughput technology
via targeted or untargeted approaches. Targeted methods utilize prior knowledge
to assess and quantify specific analytes of interest. Whereas untargeted
approaches are more discovery-based approaches to comprehensively characterize
the profiles of a biological sample. In non-gravid individuals, a recent review
on the use of omics sciences in the exercise science field highlighted the
importance of different training metrics, including exercise type, on multiomic
profiles due to the different physiological demands of the exercise59. However, much of the existing literature in pregnant individuals explores
differences in pregnancy outcomes or conditions (i.e., delivery mode, obesity,
hypertensive disorders, gestational diabetes) rather than comparing physical
activity or exercise parameters60–63.
Using metabolomic approaches, some research
exists examining the changes in metabolites and metabolic processes that occur
with physical activity in pregnancy. Briefly, habitual physical activity and
acute aerobic exercise have been found to influence metabolites in breast milk,
some of which correlated with infant growth and body composition64. A diet + exercise intervention found 132 differential metabolites in pregnant
individuals with gestational diabetes compared to the control group. Of those
identified, glycerophospholipids, steroids/steroid derivatives, fatty acyls and
carboxylic acids were among the most enriched metabolites and sphingolipid
signaling and inflammatory processes were among the enriched pathways65. Another study found that higher physical activity energy expenditure
(MET*h/day) was associated with predominantly decreased amino acids and
carbohydrates, most in the valine, leucine, isoleucine and glucose metabolic
pathways, respectively66.
Proteomics has been used to map physiological
changes to proteins across normal pregnancies67; for specific pregnancy outcomes60;
and with acute or chronic aerobic exercise68,69 and resistance
training70 in non-gravid adults. Despite this,
exploring the exercise effect in pregnancy on the gravid individual
specifically is under-researched. One study explored the proteomic changes of
acute exercise and High-Intensity Interval Training (HIIT) during pregnancy.
This study reported that 8-weeks of HIIT training led to reduced urinary
proteins following a cardiopulmonary exercise test compared to
pre-intervention. The authors highlighted that many of the reduced proteins were
related to immune system pathways, calcium ion binding and enzyme inhibitory
activity, while increased proteins were predominantly related to cellular
components71. Therefore, regular exercise during
pregnancy appears to alter the gestational parent’s proteome. However, it is
important to note that this comparison was done following an aerobic exercise
test at pre- and post-intervention and thus, does not elucidate the potential
impact of exercise training on resting physiological processes. Recent evidence
has reported that gestational exercise type differentially influences the
placental and cord blood proteomes72,73. Given
the differential effects of placental and fetal environments during pregnancy
and the differences observed following acute exercise in trained pregnant
individuals, it is plausible that there is an effect on the gestational parent
environment as well.
Collectively, the current evidence suggests
that physical activity during pregnancy may lead to metabolomic and proteomic
changes in pregnant individuals. However, due to a lack of consistency in
methodological approaches, including differences in metabolomic/proteomic
approaches, equipment, exercise parameters and biological sample type assessed,
it is difficult to fully characterize the extent of these changes. Additionally,
most of the existing literature explores physical activity in general without
examining specific exercise metrics, including exercise type. This highlights
an important gap in the literature and our understanding of the underlying
metabolic and proteomic changes that may occur with exercise during healthy
pregnancies. Thus, more research is needed to 1. better characterize biological
changes in healthy pregnant individuals and 2. characterize the differences in
exercise types to identify potential strengths and/or limitations of each for
the gestational individuals’ proteome and metabolome.
1.6. Cardiometabolic
Risk in Pregnancy
Pregnancy induces coordinated cardiovascular
and metabolic adaptations that support fetal development74,75. However, these adaptations resemble cardiometabolic
dysfunction observed in non-gravid populations (e.g., dyslipidemia, glucose
dysregulation, elevated blood pressure)76-78. As a
result, pregnancy has been conceptualized as a physiological “stress test,”
during which underlying cardiometabolic vulnerability may become apparent
earlier than in typical adult life79-83. This
period also represents a clinically relevant window for behavioral
intervention, given increased healthcare contact and engagement in
health-related behaviors84. However, since these physiological
adaptations overlap with markers traditionally used to define cardiometabolic
disease, distinguishing normal gestational changes from pathological risk
remains challenging81,84,85. This overlap complicates the interpretation
of individual cardiometabolic markers and underscores the need for integrated
approaches to risk assessment during pregnancy83.
Cardiometabolic Risk (CMR) is characterized
by the clustering of risk factors, including adiposity, high triglycerides, low
High-Density Lipoprotein (HDL), elevated blood pressure and elevated plasma
glucose86,87. These risk factors are linked through
shared underlying pathophysiological mechanisms (e.g., insulin resistance,
subclinical inflammation, altered substrate metabolism) that contribute to the
development of both metabolic and cardiovascular disease88-91. Accordingly, alterations in one component often
co-occur with or contribute to, changes in others, reflecting an integrated
risk rather than isolated abnormalities88,90,92.
This interdependence has important
implications for the assessment of cardiometabolic health during pregnancy.
While these risk factors are routinely measured in clinical settings and can
inform individualized risk profiles93,94,
evaluating them in isolation may fail to capture the cumulative burden of risk80,83,92. This limitation is particularly relevant in
pregnancy, where physiological changes in lipid metabolism, insulin sensitivity
and hemodynamics may resemble adverse cardiometabolic alterations in non-gravid
populations75,78,85. Consequently, distinguishing normal
gestational adaptation from emerging CMR remains challenging when relying on
single markers75,85. Furthermore, widely used CMR models - such
as the Framingham Risk Score - were developed in non-pregnant populations and
have been debated for their utility for women under 70 years of age81. Collectively, these highlight the need for approaches that capture the
interrelated nature of CMR, particularly within the unique context of pregnancy81,95.
Given the interrelated nature of CMR,
continuous risk scores have emerged as an approach to capture cardiometabolic
health across multiple domains93. Rather than relying
on categorical thresholds, these scores combine standardized values of
individual risk factors into a single continuous metric96. This approach may be particularly advantageous during pregnancy, where
dynamic physiological adaptations and the absence of established clinical
cut-points complicate the interpretation of individual markers74,97. By accounting for changes across cardiometabolic
domains, continuous scores may provide a more sensitive and comprehensive
assessment of cardiometabolic risk during gestation83. However, the application of continuous CMR scores in pregnancy remains
limited and important methodological considerations persist, including reliance
on sample-specific standardization, lack of external validation and uncertainty
regarding clinical thresholds74,81. While continuous approaches offer a promising
framework for evaluating CMR in pregnancy, further work is needed to establish
their validity, comparability and clinical utility within this unique
physiological context79,81.
2. Exercise Type and
Cardiometabolic Risk
Observational studies provide evidence
linking physical activity to cardiometabolic health during pregnancy. Higher
engagement in Moderate-to-Vigorous Physical Activity (MVPA) during pregnancy,
as well as reduced sedentary behavior, has been associated with more favorable
cardiometabolic profiles, including improved body composition and lower overall
risk burden5,98-100. Sandborg et al. 101 reported that greater time spent in MVPA and
lower sedentary time were associated with improved cardiometabolic health and
weight. Furthermore, increases in leisure-time physical activity also
contributed to favorable body composition and cardiometabolic health in late
pregnancy, suggesting that total movement across the intensity spectrum may be
beneficial. Similarly, Motevalizadeh et al. 83 observed that clustered CMR increased across
gestation; however, higher levels of physical activity were associated with
lower clustered CMR score. This finding highlights the potential protective
role of prenatal activity. Despite these consistent inverse associations,
important limitations must be considered. Most observational studies rely on
self-reported questionnaires or accelerometry to assess physical activity,
which may introduce measurement error and limit the ability to accurately
characterize exercise dose, intensity and modality102. As a result, while these studies support a relationship
between physical activity and CMR, they provide limited insight into the
specific exercise prescription necessary to optimize cardiometabolic health
during pregnancy.
Intervention studies provide insight into the
potential effects of prenatal exercise on cardiometabolic health; however, most
are designed as behavioral interventions designed to increase overall physical
activity or improve lifestyle patterns rather than isolate the effects of
specific exercise prescriptions101,103. This
limits the ability to determine how specific exercise characteristics - such as
mode - independently influence gestational CMR. Although some modality-specific
interventions have been examined, findings are primarily limited to individual
cardiometabolic markers. Aerobic exercise has been associated with reduced
gestational weight gain and improved insulin response104,105. Whereas combined aerobic and resistance training has
demonstrated improvements in cardiorespiratory fitness, LDL and triglyceride
levels. Despite these favorable changes, most intervention studies do not
assess composite CMR, limiting insight into how exercise influences the overall
cardiometabolic profile during pregnancy. As a result, it remains unclear
whether specific exercise modes or prescriptions differentially impact
composite CMR across gestation.
While numerous CMR prediction models have
been published, these frameworks were developed largely in non-pregnant
populations81,94. This absence of pregnancy-specific CMR
assessment makes it difficult to accurately define normal gestational
physiological adaptation versus meaningful variation in CMR74. As a result, there is no consensus on which variables should be
included in a pregnancy-specific CMR score or how risk should be interpreted
across gestation. Without a standardized framework, findings are difficult to
compare across the literature. There is also a limited use of composite CMR in
prenatal research, which restricts the understanding of how exercise influences
overall pregnancy CMR rather than isolated physiological markers83. Most prenatal exercise studies evaluate isolated outcomes such as
gestational weight gain, glucose tolerance, blood pressure or lipids rather
than clustered CMR. Although these findings are informative, they fail to
capture the cumulative burden and multidimensional nature of CMR. This limits
the ability to determine whether interventions meaningfully alter pregnancy
CMR. In addition, the lack of well-characterized exercise prescription,
particularly with respect to mode, dose and supervised delivery, hinders the
development of targeted prenatal exercise recommendations, specifically in the
context of reducing CMR5,100,106. Observational studies rely on self-report
or accelerometry and many intervention studies are designed to increase general
activity or improve lifestyle behaviors, making it difficult to understand the
isolated effects of structured exercise. Without specificity in prescription,
it is difficult to translate findings into practical clinical recommendations.
Finally, the scarcity of longitudinal parent and offspring follow-up restricts
understanding of the long-term effect of prenatal exercise on cardiometabolic
health for the pregnant individual and offspring. Most studies stop at
delivery, limiting the ability to define whether prenatal cardiometabolic
adaptations persist postpartum as well as elucidate the effect of gestational
exercise on offspring cardiometabolic health beyond birth. Together, these gaps
highlight the need for improved, pregnancy-specific CMR assessment and
precisely defined exercise interventions to better understand and optimize
cardiometabolic health in pregnancy and early life.
3. Prenatal Exercise Types and Placental
Outcomes
3.1. Placental growth, vascular function and
efficiency
Placental
growth and morphology reflect integrated adaptations in uteroplacental
perfusion, vascular function and exchange efficiency - processes that may
respond differently to different exercise modalities (i.e., aerobic, resistance
or combination of both) during pregnancy. Available evidence indicates that
prenatal exercise does not adversely affect placental growth. Despite this,
evidence regarding the impact of different exercise modalities is lacking.
Commonly reported outcomes of placental growth include Placental Weight (PW)
and birthweight to placental weight ratio (BW-to-PW), which represents a
measurement of placental efficiency. Evidence in pregnant women demonstrates
that women who averaged at least 150 minutes of exercise per week during
pregnancy had lower placental weight compared to their inactive counterparts107. A meta-analysis
conducted by Kubler et al.108 of 9 studies (7 randomized controlled trials and 2
cohort studies), including 44,102 women, investigated the effect of prenatal
exercise on placental composition and reported no difference in placental
weight or the placental weight to birth weight ratio between women who
exercised during pregnancy and their non-exercising counterparts.
Interestingly, when stratified by exercise modality, women who performed
combined aerobic and resistance exercise tended (p=0.06) to have lower
placental weight compared to non-exercising women, but women who performed
aerobic exercise had similar placental weight to non-exercisers. Furthermore,
when stratified by exercise intensity, placental weight for women performing
low-to-moderate intensity exercise tended to be lower than that of non-exercisers,
whereas women performing moderate intensity exercise tended (p=0.08) to have
higher placental weights compared to non-exercisers. Findings from another study
demonstrate that in comparison to non-exercising women, those who performed
combination exercise had significantly lower placental weight and higher
placental efficiency109.
Placental weight has also been associated with maternal exercise frequency, where
placental weight decreases with increasing frequency of exercise110. Additionally, a
positive relationship exists between increased exercise volume and increased
placental volume (i.e., greater exercise volume corresponds to greater
placental volume)111.
Exercise volume also plays a role in altering the placental proteome112.
Across
randomized controlled trials, aerobic exercise does not consistently alter
absolute placental weight, indicating that functional improvements
may occur without changes in gross placental mass108,113. However, very
high exercise volumes or intensities performed late in pregnancy have been
associated with transient reductions in uterine and umbilical blood flow,
particularly when exercise intensity approaches maximal maternal capacity114.
Evidence regarding resistance and weight-bearing exercise suggests
gestational age-dependent effects on placental and fetoplacental growth.
Moderate resistance exercise initiated in early pregnancy has been
associated with increased fetoplacental growth rates, particularly in women who
were physically active before conception108. In contrast, sustained high-volume or
high-intensity weight-bearing exercise during mid to late gestation has been
linked to reduced fetoplacental growth and lower umbilical blood
flow, indicating possible adaptive or restrictive placental responses
to increased metabolic demand108,114. Reductions in exercise volume during late pregnancy
have been shown to reverse these effects and restore fetoplacental growth
trajectories108. The
effects of resistance exercise on placental weight remain inconsistent, with
several studies reporting no significant differences between exercising and
non-exercising groups108,113.
Resistance exercise performed in the supine position remains a
concern due to potential reductions in uteroplacental blood flow115. Combined
aerobic and resistance exercise programs are commonly prescribed during
pregnancy, although placental-specific outcomes are
less frequently reported independently116. Available evidence suggests that
moderate-intensity combined exercise supports placental functional capacity
by maintaining endothelial function and uteroplacental perfusion117. These
physiological adaptations may contribute to improved placental efficiency and reduced
risk of fetal compromise by supporting effective maternal-fetal exchange114. However,
inconsistent reporting of placental endpoints limits
conclusions regarding the independent effects of combined exercise
modalities118.
Building
on structural adaptations, exercise during pregnancy may also influence
uteroplacental blood flow and vascular function, thereby shaping the delivery
of oxygen and nutrients to the developing fetus. Specifically, aerobic exercise
during pregnancy has been consistently associated with improvements in
uteroplacental and umbilical blood flow, suggesting enhanced placental
perfusion and exchange capacity114,115. Doppler ultrasound studies summarized in multiple
reviews indicate that aerobic exercise reduces placental vascular resistance,
reflected by favorable umbilical artery systolic/diastolic ratios108. Moderate-intensity
aerobic exercise initiated in early pregnancy has been shown to
support placental circulation and fetal cardiovascular adaptation, likely
mediated by improved maternal hemodynamics115. Structural adaptations, including
increased villous vascularization and preservation of placental parenchymal
tissue, have been reported among women engaging in regular aerobic activity108. Evidence in
pregnant women demonstrates that placentas of women who averaged at least 150
minutes of exercise per week during pregnancy have increased placental protein
and mRNA expression of vascular endothelial growth factor (VEGF), an angiogenic
growth mediator, compared to their inactive counterparts107, which suggests
that exercise during pregnancy increases placental vascular development
(vasculogenesis and angiogenesis). Furthermore, findings from preclinical
models of maternal obesity suggest that exercise may protect the placenta from
the adverse effects of maternal obesity on placental vascularization119. Additionally,
regular maternal exercise has been shown to increase placental villous area,
which aids in the maintenance of fetal oxygen and substrate availability120.
3.2. Placental Mitochondrial Metabolism, Redox
Balance and Nutrient Transport
At
the cellular level, emerging evidence indicates that placental mitochondrial
function and metabolic regulation may respond differently to prenatal exercise
modality, reflecting variation in metabolic demand and energetic stress across
exercise types. Considering aerobic exercise predominantly utilizes oxidative
metabolism, while resistance exercise primarily utilizes anaerobic pathways, it
is plausible that different modes of exercise elicit different placental
adaptations. Findings from preclinical models that examined the impact of
prenatal aerobic exercise (treadmill) on primary placental trophoblast cells
demonstrate increased peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α)
activation in trophoblasts of exercising rodents, as well as increased
mitochondrial biogenesis and oxidative metabolism121. Combined aerobic and resistance
(combination) exercise during pregnancy is also shown to elicit beneficial
effects on placental mitochondria. Specifically, findings demonstrate that
compared to non-exercising women, placentas of women who performed combination
exercise during pregnancy had higher mitochondrial DNA (mtDNA) copy number and
lower mtDNA deletions122.
Interestingly, the placentas from combination exercisers also had significantly
higher concentrations of manganese - an important mineral present in
mitochondrial antioxidant Superoxide Dismutase (SOD) - which also corresponded
with greater mtDNA density and lower mtDNA deletions122.
Adaptations
to placental mitochondria are inherently accompanied by alterations in Reactive
Oxygen Species (ROS) production and redox balance, both of which are important
for maintaining placental signaling mechanisms. However, excess ROS production,
as well as low antioxidant buffering capacity, can lead to oxidative stress,
which may negatively affect placental function. Mitochondria are major
producers of ROS and mitochondrial ROS production helps provide a balance of
pro-angiogenic and anti-angiogenic growth factors. Considering how different
exercise modalities vary in their metabolic intensity and reliance on oxidative
pathways, prenatal exercise type may differentially influence placental ROS
production and redox balance. A placental transcriptomic analysis of placental
tissue from women who performed moderate-intensity cycling at the recommended
levels revealed an upregulation of antioxidant genes and downregulation of
pro-inflammatory genes with exercise, which may help regulate placental redox
balance and reduce oxidative stress123. A different study investigated the impact of combination
exercise during pregnancy and reported that combination exercise leads to a
4-fold increase in Nitric Oxide (NO) production and a 2-fold increase in
endothelial NOS (eNOS) expression in placental cytosol109. Placental
mitochondria from women who performed combination exercise also had decreased
levels of mitochondrial superoxide and decreased H2O2 production rate109. Together, these results suggest that
aerobic and combination exercise may both help decrease placental oxidative
stress by increasing antioxidants while decreasing ROS production and
inflammation.
The
placenta actively regulates nutrient allocation to the fetus through tightly
controlled transport systems and energy-sensing pathways that integrate
maternal metabolic signals, including those altered by exercise124. The placenta uses
intrinsic nutrient sensors, including AMP-Activated Protein Kinase (AMPK) and
mammalian target of rapamycin (mTOR), which respond to changes in maternal
hormone levels, particularly insulin-like growth factor 1 (IGF-1), insulin,
leptin, adiponectin, cortisol and cytokines125. Importantly, the placenta’s ability to
sense changes in maternal nutrient supply (i.e., overnutrition, undernutrition)
enables it to balance fetal nutrient demand with maternal nutrient supply125. The mTOR signaling
pathway plays a key role in regulating the expression of nutrient transporters
in response to nutrient availability, exercise and the signaling of growth
factors such as IGF-1126.
Considering exercise elicits hormonal changes, it is plausible that
exercise-induced changes in levels of circulating maternal hormones impact
placental nutrient-sensing pathways. The regulation of placental nutrient
transport and energy-sensing pathways, including mTOR and AMPK, may be
particularly sensitive to prenatal exercise modality, as different exercise
types impose distinct anabolic and energetic signals on the maternal-placental
unit. Current evidence demonstrates that placentas from women who met physical
activity guidelines during pregnancy had lower gene expression of fatty acid
transport protein 4 (FATP4), IGF-1 and AMPK and higher expression of SNAT2127. Interestingly,
this study also reported correlations with maternal sugar intake, where sugar
intake positively correlated with GLUT1 expression and inversely correlated
with mTOR and IGF-1 expression, which highlights the role of dietary intake in
addition to maternal exercise in placental nutrient transport127. Findings from
preclinical models of prenatal resistance exercise show increased expression of
placental glucose transporters GLUT1 and GLUT3, increased expression of amino
acid transporters SNAT1 and SNAT2 and increased mTOR expression in response to
resistance training during pregnancy128.
3.3. Placentokine-exerkine crosstalk
In
addition to metabolic and transport roles, the placenta functions as an endocrine
organ and exercise during pregnancy may influence placental hormone secretion
and signaling. Cytokines secreted by the placenta, termed placentokines,
including apelin, SOD3, irisin,
leptin, chemerin and adiponectin, mediate fetal development and maternal
metabolism129,130.
Furthermore, evidence from non-pregnant individuals demonstrates the
differential impact of exercise modality on exerkines (cytokines elicited by
exercise) - aerobic exercise primarily elicits hormonal responses that
facilitate substrate mobilization and metabolic homeostasis, whereas resistance
exercise preferentially stimulates anabolic and tissue-remodeling hormones.
Considering the difference in hormonal response between exercise modalities, it
is plausible that distinct prenatal exercise modalities may differentially
alter placental endocrine function and placentokine signaling, potentially
mediating modality-specific communication between maternal tissues, the
placenta and the developing fetus. It is also possible that modality-specific
exerkines may differentially impact the placenta by influencing trophoblast
function and uteroplacental blood flow131.
4. Limitations and Considerations
Despite
increasing evidence that prenatal exercise induces adaptive placental remodeling
in a modality-specific manner, several limitations should be considered. It is
important to note that much of the evidence describing exercise-induced
placental adaptations is derived from indirect measures, such as Doppler
ultrasound indices and placental weight ratios, rather than direct histological
assessments. Resistance exercise and high-intensity interval training protocols
remain underrepresented and few studies are explicitly designed to compare
exercise modalities. In addition, placental outcomes are inconsistently
reported and potential sex-specific placental responses are rarely examined.
Considering factors like preconception exercise habits, exercise volume and
timepoint during gestation can all modify the effects of exercise on placental
growth and function132,
standardized reporting of exercise modality, intensity, timing and placental
endpoints will be essential to advance the current knowledge base of
modality-specific placental mechanisms and outcomes.
4.1. Prenatal Exercise Types and offspring Outcomes
Current recommendations from the
American College of Obstetrics and Gynecologists state that while some
modifications to exercise may be necessary due to physiologic changes that
occur during pregnancy, exercise is generally safe and encouraged5. Evidence suggests that exercise during pregnancy can
plausibly influence the body composition of offspring and potentially also
influence early childhood lipid biology. While specific pathways of influence
remain unclear, possible theories include prenatal exercise leading to improved
maternal glucose and lipid metabolism, leading to reduced risk for gestational
hyperglycemia or hyperlipidemia. Additionally, influences on offspring outcomes
may also be due to prenatal exercise causing changes in fetal metabolic
programming.
While there is some evidence to
suggest linkages between prenatal exercise and associations with body
composition outcomes of the offspring, data is limited in both quantity and
scope. Findings suggest exercise during pregnancy is associated with a
reduction in macrosomia in the offspring, as well as Large-for-Gestational Age (LGA)133. Both macrosomia and LGA are associated with a higher risk
of morbidity and mortality of the offspring134.
Moreover, studies investigating the neonatal body composition overall provide
mixed evidence. Generally, greater activity levels during pregnancy are
associated with lower levels of neonatal adiposity135. This relationship is also suggested to be stronger when
observed in mothers with higher-risk conditions during pregnancy, such as
obesity136. Interestingly, long-term follow-up
on these effects is limited and has mixed results, with some trials showing no
difference in adiposity in childhood, while others report higher adiposity in
the exercise group; however, it should be noted that the result was reported as
an outlier in a smaller sample size137-139.
The data on offspring lipid profiles are also very limited, but some
observational studies report an increase in High-Density Lipoprotein
Cholesterol (HDL-C) with increased maternal activity140. While prenatal exercise can broadly influence metabolic
outcomes on cardiac health, exercise-specific connections remain
underinvestigated141. It is also important to note that
many studies currently in the literature utilize birth weight or Body Mass
Index (BMI) as a metric for adiposity. Studies utilizing more direct measures
of adiposity, such as skinfold measurements or dual-energy X-ray absorptiometry
(DXA), report that in some cases, maternal exercise may reflect no changes in
birthweight but may cause changes in fat mass and fat-free mass overall135.
The current literature is also sparse in investigations into the influence of types of exercise on child body composition outcomes. Some studies have found that aerobic activity, such as walking, cycling, swimming, etc., is correlated with a lower risk of macrosomia or LGA at a population level133,134. Additionally, aerobic activity has been associated with negligible changes in the actual birth weight average, but possible decreased in overall neonatal fat mass in studies that have used direct adiposity measures as previously mentioned133-135. When considering resistance exercise, studies investigating resistance-only programs of exercise are relatively rare, with more studies combining aerobic exercise with resistance for overall conditioning. What is known is that resistance training can improve maternal insulin sensitivity and help limit excessive gestational weight gain, both of which are factors that may influence fetal lipid accumulation5,142. However, since resistance-only exposure is rare in the literature, conclusions regarding the specific influence of this exercise type on children’s body compositions remain unclear. Conversely, combined aerobic and resistance exercise programs seem to be the most widely studied in this population, with more evidence to support a connection between exercise and child body composition. In a trial studying pregnant mothers with obesity, combined exercise was associated with lower cellular and whole-body adiposity measures in offspring136. There is mixed evidence to support this relationship when looking at early childhood populations. One study found that combination exercise in obese mothers was not associated with any detectable change in offspring anthropometrics at 2 and 3 years old139. However, another study reported an increase in regional adiposity at roughly 7-year-old offspring born to mothers who did exercise during pregnancy137. These mixed results may suggest that combined exercise programs may improve perinatal risk factors, such as macrosomia, but may not have durable effects on adiposity or body composition into childhood and may also be dependent on postnatal environment, maternal risk factors and exercise timing and quantity133-135,137,139.
5. Funding: This research was supported by the internal funds from ECU (PI: Linda May).
6. References