Fetal programming: Difference between revisions

Revision as of 16:04, 24 July 2024

Latest revision as of 22:55, 29 March 2025

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{{Short description|Theory that suggests environmentenvironmental factors during fetal development affect disease risks}}

'''Fetal programming''', also known as '''prenatal programming''', is the theory that environmental cues experienced during fetal development play a seminal role in determining health trajectories across the lifespan.

Three main forms of programming that occur due to changes in the maternal environment are:

* Changes in development that lead to greater disease risk;

* Genetic changes whichthat alter disease risk;

* [[Epigenetics|Epigenetic]] changes which alter disease risk of not only the child but also that of the next generation - i.e., after a famine, grandchildren of women who were pregnant during the famine, are born smaller than the normal size, despite nutritional deficiencies having been fulfilled.

These changes in the maternal environmental can be due to nutritional alteration,<ref name = "Fleming_2012">{{cite journal | vauthors = Fleming TP, Velazquez MA, Eckert JJ, Lucas ES, Watkins AJ | title = Nutrition of females during the peri-conceptional period and effects on foetal programming and health of offspring | journal = Animal Reproduction Science | volume = 130 | issue = 3–4 | pages = 193–7 | date = February 2012 | pmid = 22341375 | doi = 10.1016/j.anireprosci.2012.01.015 }}</ref> hormonal fluctuations<ref>{{cite journal | vauthors = Talge NM, Neal C, Glover V | title = Antenatal maternal stress and long-term effects on child neurodevelopment: how and why? | journal = Journal of Child Psychology and Psychiatry, and Allied Disciplines | volume = 48 | issue = 3–4 | pages = 245–61 | date = March 2007 | pmid = 17355398 | doi = 10.1111/j.1469-7610.2006.01714.x | pmc = 11016282 }}</ref> or exposure to toxins.

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== History ==

=== Dutch famine 1944–45 ===

In 1944–45, the German blockade of the Netherlands led to a lack of food supplies, causing the [[Dutch famine of 1944–45]]. The famine caused severe malnutrition among the population, including women in various stages of pregnancy. The Dutch Famine Birth Cohort Study examined the impact of lack of nutrition on children born during or after this famine. It showed that over the course ofthroughout their life, these children were at greater risk of [[Diabetes mellitus|diabetes]], [[cardiovascular disease]], [[obesity]], and other [[non-communicable disease]]s.{{citation needed|date=April 2023}}

=== Barker hypothesis ===

In the 1980s, [[David Barker (epidemiologist)|David Barker]] began a research study on this topic. The Barker Hypothesis, or [[Thrifty phenotype]], forms the basis for much of the research conducted on fetal programming. This hypothesis states that if the fetus is exposed to low nutrition, it will adapt to that particular environment. Nutrients are diverted towards the development of thedeveloping heart, brain, and other essential fetal organs of the fetus. The body also undergoes metabolic alterations that ensure survival in spite ofdespite low nutrition but may cause problems in situations with normal or high nutrition.<ref>{{cite journal | vauthors = Remacle C, Bieswal F, Reusens B | title = Programming of obesity and cardiovascular disease | journal = International Journal of Obesity and Related Metabolic Disorders | volume = 28 Suppl 3 | issue = S3 | pages = S46-53 | date = November 2004 | pmid = 15543219 | doi = 10.1038/sj.ijo.0802800 | doi-access = free }}</ref> This leads to increased risk of [[metabolic syndrome]].

== Nutritional status ==

The developing fetus forms an impression of the world into which it will be born via its mother's nutritional status. Its development is thus modulated to create the best chance of survival. However, excessive or insufficient nutrition in the mother can provoke maladaptive developmental responses in the fetus, which in turn manifest in the form of post-natal diseases. ItThis ismay possible that this hashave such a profound effect on the fetus’fetus’s adult life that it can even outweigh lifestyle factors.<ref name = "Fleming_2012" />

=== Excessive nutrition ===

[[Body mass index]] prior tobefore pregnancy and weight gain during pregnancy are both linked to high blood pressure in the offspring during adulthood. Mouse models suggest that this is due to high levels of the fetal hormone [[leptin]], which is present in the blood of individuals thatwho are overweight or obese. There is a theory that this hormone has a negative impact onhurts the regulatory systems of the fetus, and renders it impossible to maintain normal blood pressure levels.<ref>{{cite journal | vauthors = Taylor PD, Samuelsson AM, Poston L | title = Maternal obesity and the developmental programming of hypertension: a role for leptin | journal = Acta Physiologica | volume = 210 | issue = 3 | pages = 508–23 | date = March 2014 | pmid = 24433239 | doi = 10.1111/apha.12223 | s2cid = 22295003 | doi-access = free }}</ref>

=== Insufficient nutrition ===

[[Pre-eclampsia]], involving oxygen deprivation and death of [[Trophoblast|trophoblastic cells]] that make up most of the placenta, is a disease which is often associated with maladaptive long-term consequences of inappropriate fetal programming. Here, an inadequately developed and poorly functioning placenta fails to meet the fetus’fetus’s nutritional needs during gestation, either by altering its selection for nutrients whichthat can cross into fetal blood or restricting total volume thereof. Consequences of this for the fetus in adult life include cardiovascular and metabolic conditions.<ref>{{cite journal | vauthors = Myatt L | title = Placental adaptive responses and fetal programming | journal = The Journal of Physiology | volume = 572 | issue = Pt 1 | pages = 25–30 | date = April 2006 | pmid = 16469781 | pmc = 1779654 | doi = 10.1113/jphysiol.2006.104968 }}</ref>

== Hormonal influence ==

A delicate balance of hormones during pregnancy is regarded as being highly relevant to fetal programming and may significantly influence the outcome onof the offspring.<ref name="Hoffman_2016">{{cite journal | vauthors = Hoffman MC | title = Stress, the Placenta, and Fetal Programming of Behavior: Genes' First Encounter With the Environment | journal = The American Journal of Psychiatry | volume = 173 | issue = 7 | pages = 655–7 | date = July 2016 | pmid = 27363547 | doi = 10.1176/appi.ajp.2016.16050502 | doi-access = free }}</ref> Placental endocrine transfer from the mother to the developing fetus could be altered by the mental state of the mother, due to affected [[glucocorticoid]] transfer that takes place across the placenta.<ref name="Hoffman_2016" />

=== Thyroid ===

Thyroid hormones play an instrumental role during the early development of the fetus's brain. Therefore, mothers suffering from thyroid-related issues and altered thyroid hormone levels may inadvertently trigger structural and functional changes in the fetal brain. The fetus is able tocan produce its own thyroid hormones from the onset of the second trimester; however, maternal thyroid hormones are important for brain development before and after the baby is able tocan synthesize the hormones while still in the uterus.<ref name="Andersen_2016">{{cite journal | vauthors = Andersen SL, Olsen J, Laurberg P | title = Foetal programming by maternal thyroid disease | journal = Clinical Endocrinology | volume = 83 | issue = 6 | pages = 751–8 | date = December 2015 | pmid = 25682985 | doi = 10.1111/cen.12744 | s2cid = 32873121 | doi-access = free }}</ref> Due to this, the baby may experience an increased risk of neurological or psychiatric diseases later in life.<ref name="Andersen_2016" />

=== Cortisol ===

Cortisol (and glucocorticoids more generally) is the most well -studied hormonal mechanism that may have prenatal programming effects.<ref>{{cite journal | vauthors = Moisiadis VG, Matthews SG | title = Glucocorticoids and fetal programming part 2: Mechanisms | journal = Nature Reviews. Endocrinology | volume = 10 | issue = 7 | pages = 403–11 | date = July 2014 | pmid = 24863383 | doi = 10.1038/nrendo.2014.74 | s2cid = 11475810 }}</ref> Although cortisol has normative developmental effects during prenatal development, excess cortisol exposure has deleterious effects on fetal growth,<ref>{{cite journal | vauthors = O'Donnell KJ, Meaney MJ | title = Fetal Origins of Mental Health: The Developmental Origins of Health and Disease Hypothesis | journal = The American Journal of Psychiatry | volume = 174 | issue = 4 | pages = 319–328 | date = April 2017 | pmid = 27838934 | doi = 10.1176/appi.ajp.2016.16020138 | doi-access = free }}</ref> the postnatal function of physiological systems such as the hypothalamic-pituitary-adrenal axis <ref>{{cite journal | vauthors = Kapoor A, Petropoulos S, Matthews SG | title = Fetal programming of hypothalamic-pituitary-adrenal (HPA) axis function and behavior by synthetic glucocorticoids | journal = Brain Research Reviews | volume = 57 | issue = 2 | pages = 586–95 | date = March 2008 | pmid = 17716742 | doi = 10.1016/j.brainresrev.2007.06.013 | s2cid = 30865698 }}</ref> and brain structure or connectivity (e.g., amygdala).<ref>{{cite journal | vauthors = Buss C, Davis EP, Shahbaba B, Pruessner JC, Head K, Sandman CA | title = Maternal cortisol over the course of pregnancy and subsequent child amygdala and hippocampus volumes and affective problems | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 109 | issue = 20 | pages = E1312-9 | date = May 2012 | pmid = 22529357 | pmc = 3356611 | doi = 10.1073/pnas.1201295109 | doi-access = free }}</ref><ref>{{cite journal | vauthors = Graham AM, Rasmussen JM, Entringer S, Ben Ward E, Rudolph MD, Gilmore JH, Styner M, Wadhwa PD, Fair DA, Buss C | display-authors = 6 | title = Maternal Cortisol Concentrations During Pregnancy and Sex-Specific Associations With Neonatal Amygdala Connectivity and Emerging Internalizing Behaviors | journal = Biological Psychiatry | volume = 85 | issue = 2 | pages = 172–181 | date = January 2019 | pmid = 30122286 | pmc = 6632079 | doi = 10.1016/j.biopsych.2018.06.023 }}</ref>

During gestation, cortisol concentrations in maternal circulation are up to ten times higher than cortisol concentrations in fetal circulation.<ref>{{cite journal | vauthors = Travers S, Martinerie L, Boileau P, Xue QY, Lombès M, Pussard E | title = Comparative profiling of adrenal steroids in maternal and umbilical cord blood | journal = The Journal of Steroid Biochemistry and Molecular Biology | volume = 178 | pages = 127–134 | date = April 2018 | pmid = 29191401 | doi = 10.1016/j.jsbmb.2017.11.012 | s2cid = 3705475 }}</ref> The maternal-to-fetal cortisol gradient is maintained by the placenta, which forms a structural and enzymatic barrier to cortisol.<ref>{{cite journal | vauthors = Chapman K, Holmes M, Seckl J | title = 11β-hydroxysteroid dehydrogenases: intracellular gate-keepers of tissue glucocorticoid action | journal = Physiological Reviews | volume = 93 | issue = 3 | pages = 1139–206 | date = July 2013 | pmid = 23899562 | pmc = 3962546 | doi = 10.1152/physrev.00020.2012 }}</ref><ref>{{cite journal | vauthors = Stirrat LI, Sengers BG, Norman JE, Homer NZ, Andrew R, Lewis RM, Reynolds RM | title = Transfer and Metabolism of Cortisol by the Isolated Perfused Human Placenta | journal = The Journal of Clinical Endocrinology and Metabolism | volume = 103 | issue = 2 | pages = 640–648 | date = February 2018 | pmid = 29161409 | pmc = 5800837 | doi = 10.1210/jc.2017-02140 }}</ref> During the first two trimesters of gestation intrauterine cortisol is primarily produced by the maternal adrenal glands.<ref name="Development and function of the hum">{{cite journal | vauthors = Ishimoto H, Jaffe RB | title = Development and function of the human fetal adrenal cortex: a key component in the feto-placental unit | journal = Endocrine Reviews | volume = 32 | issue = 3 | pages = 317–55 | date = June 2011 | pmid = 21051591 | pmc = 3365797 | doi = 10.1210/er.2010-0001 }}</ref> However, during the third trimester the fetal adrenal glands begin to endogenously produce cortisol and become responsible for most intrauterine cortisol by the time the fetus reaches term.<ref name="Development and function of the hum"/>

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=== Psychological stress ===

Maternally experienced psychological stress that occurs either prior tobefore or during gestation can have intergenerational effects on offspring. Stress experienced during gestation has been linked with preterm delivery, low birth weight, and increased risk of psychopathology.<ref name="Hoffman_2016" /> The new mother may suffer from after-effects too, such as postpartum depression, and subsequently may find parenting more difficult as compared to those who did not experience as much stress during their pregnancies.<ref name="Hoffman_2016" />

== Toxins ==

Toxins such as alcohol, tobacco, and certain drugs to which the baby is exposed to during its development are thought to contribute to fetal programming, especially via alterations to the HPA axis.<ref name="Bekdash_2014">{{cite journal | vauthors = Bekdash R, Zhang C, Sarkar D | title = Fetal alcohol programming of hypothalamic proopiomelanocortin system by epigenetic mechanisms and later life vulnerability to stress | journal = Alcoholism: Clinical and Experimental Research | volume = 38 | issue = 9 | pages = 2323–30 | date = September 2014 | pmid = 25069392 | pmc = 4177357 | doi = 10.1111/acer.12497 }}</ref> If the exposure occurs during a critical phase of fetal development, it could have drastic and dire consequences for the fetus.<ref name="Bekdash_2014" />

=== Alcohol ===

Prenatal and/or early postnatal exposure to alcohol (ethanol) has been found to havehurt a negative effect on child's neuroendocrine and behavioral factors.<ref name="Weinberg_2008">{{cite journal | vauthors = Weinberg J, Sliwowska JH, Lan N, Hellemans KG | title = Prenatal alcohol exposure: foetal programming, the hypothalamic-pituitary-adrenal axis and sex differences in outcome | journal = Journal of Neuroendocrinology | volume = 20 | issue = 4 | pages = 470–88 | date = April 2008 | pmid = 18266938 | doi = 10.1111/j.1365-2826.2008.01669.x | pmc = 8942074 | s2cid = 4574957 }}</ref> Alcohol passes through the placenta on being ingested by the mother during her pregnancy, and makes its way to the baby ''in utero''.<ref name="Weinberg_2008" /> Changes posed to the fetus through ethanol exposure may significantly effect growth and development; these are collectively known as fetal alcohol spectrum disorders (FASD).<ref name="Weinberg_2008" /> The exact interaction between ethanol and the developing fetus is complex and largely uncertain, however, several direct and indirect effects have been observed as the fetus matures.<ref name="Weinberg_2008" /> Predominant among these are irregularities in the fetus's endocrine, metabolic, and physiological functions.<ref name="Weinberg_2008" />

=== Smoking ===

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=== Drugs ===

There is evidence pointing towards pharmacological programming of the fetus during the first trimester.<ref name="Bayliss_2002">{{cite journal | vauthors = Bayliss H, Churchill D, Beevers M, Beevers DG | title = Anti-hypertensive drugs in pregnancy and fetal growth: evidence for "pharmacological programming" in the first trimester? | journal = Hypertension in Pregnancy | volume = 21 | issue = 2 | pages = 161–74 | date = January 2002 | pmid = 12175444 | doi = 10.1081/prg-120013785 | s2cid = 30016072 }}</ref> One type of drugs which is suspected of influencing the developing baby when used during pregnancy is anti-hypertensive drugs.<ref name="Bayliss_2002" /> Pre-eclampsia (a condition of hypertension during pregnancy), is a serious problem for the majority of pregnant mothers and can predispose the mother to a variety of complications, including increased risk of mortality and problems during parturition.<ref name="Bayliss_2002" />

== References ==