THE TWO FACES OF PERINATAL EPIDEMIOLOGY - PowerPoint PPT Presentation

1 / 35
About This Presentation
Title:

THE TWO FACES OF PERINATAL EPIDEMIOLOGY

Description:

WHY SHIFTY AND NIFTY? ... NIFTY MATERNOTYPE = a genotype rich in genes that promote maternal survival ... EXAMPLE OF A NIFTY MATERNOTYPE AFFECTING CVD RISK ... – PowerPoint PPT presentation

Number of Views:230
Avg rating:3.0/5.0
Slides: 36
Provided by: Epidem3
Category:

less

Transcript and Presenter's Notes

Title: THE TWO FACES OF PERINATAL EPIDEMIOLOGY


1
THE TWO FACES OF PERINATAL EPIDEMIOLOGY
  • Nigel Paneth
  • NIH-CHIR course in
  • Reproductive and Perinatal Epidemiology
  • Woods Hole, MA
  • July 14, 2005
  • http//www.epi.msu.edu/faculty/paneth.htm

2
WHAT DOES PERINATAL REFER TO?
  • Classical definition
  • The period from 28 weeks of gestation to age one
    week
  • Expanded definition
  • The period from 20 weeks of gestation to age one
    month
  • My more conceptual definition
  • Phenomena that take place from the time the
    organs are formed (fetal life) until the baby has
    adapted to post-natal life (the first few months)

3
THREE KEY CONCEPTS PERTAINING TO THE PERINATAL
PERIOD
  • Competition
  • In some ways, the fetus/baby and the mother
    compete for resources and for survival. At times
    two or more fetuses may compete with each other
    for resources.
  • Adaptation
  • The fetus must adapt to labor and to
    extra-uterine life. The mother must adapt to the
    stresses of labor.
  • Magnification
  • Events taking place in the perinatal period may
    have magnified impacts on later development

4
COMPETITION
  • Mother and fetus/baby should ideally both
    survive, but the fetus is in competition with
    mother for nutrients and at times may have
    different metabolic or physiologic priorities.
    Under nearly all circumstances, mothers survival
    will take precedence over the baby. Some fetal
    conditions may reflect the maternal need to
    survive.
  • EXAMPLE Below a threshold of 1,500 calories per
    day, preservation of maternal weight takes
    precedence over fetal growth

5
ADAPTATION
  • Both mother and fetus must pass through some key
    passages during the perinatal period. Failure to
    adapt to the requirements of these passages will
    lead to death or damage to mother or fetus
  • EXAMPLES
  • Maternal passage through labor
  • Fetal passage through labor
  • Fetal adaptation to post-natal breathing

6
MAGNIFICATION
  • The fetus grows and develops rapidly, and it is
    possible that exposures occurring at certain
    times will be much more important than those that
    occur at less sensitive periods of development.
  • EXAMPLE lack of thyroid hormone during the
    second trimester may permanently damage white
    matter

7
EPIDEMIOLOGICAL IMPLICATIONS OF THESE CONCEPTS
  • Stress - The normal fetus undergoes a period of
    extreme asphyxial stress in labor, while the
    delivering mother experiences the most extreme
    hemorrhagic stress of ordinary human experience.
  • Risk For both mothers and babies, labor is the
    period of time in life when the risk of dying is
    highest.

8
STRESS
  • ASPHYXIA Stanley James and Virginia Apgar at
    Columbia showed in the 1950s that normal labors
    are asphyxiating. Even a very healthy newborn can
    have blood gas values at birth that if found in a
    child or adult would mandate immediate admission
    to intensive care.
  • HEMORRHAGE In underdeveloped countries,
    bleeding is the leading cause of maternal death.
    Even in developed countries, 5 or so of mothers
    lose more than a liter of blood in delivery.
  • Magann EF et al Postpartum hemorrhage after
    vaginal birth an analysis of risk factors. South
    Med J. 2005 98419-22

9
RISK OF FETAL DEATH IN LABOR
  • Intrapartum fetal death rates (death between the
    onset of labor and birth) tend to be around 1 per
    thousand babies entering labor in developed
    countries.
  • If the average duration of labor is 12 hours, an
    intrapartum fetal mortality rate of 5/1,000
    fetuses at risk (a rate recently found in rural
    China1), means that the death rate of labor can
    be as high as 1 per day.
  • Even at a Canadian tertiary care center, a recent
    intrapartum fetal death rate was found to be
    0.65/1,000.2
  • This daily rate of death is not even found at age
    100.
  • Wen SW et al J Perinatol. 2004 Feb24(2)77-81.
  • Mattatall FM et al Am J Obstet Gynecol. 2005
    May192(5)1475-7

10
ORDINARY LABOR IS AS RISKY TO FETAL LIFE AS A
SEVERE EPIDEMIC/DISASTER SITUATION
  • Only the worst epidemic situations come close to
    labor in terms of risk of death.
  • In the highest mortality South Darfur town,
    mortality under age five in late 2004 was
    0.59/1,000/day, half the rate of death for
    fetuses in Canadian tertiary care
  • Grandesso F et al JAMA. 20052931490-4.

11
MATERNAL MORTALITY
  • Maternal mortality rates (most of which are
    related to labor and delivery in undeveloped
    countries) differ more between developed and
    underdeveloped countries than any other mortality
    measure.
  • Maternal mortality rates declined more than any
    other population mortality parameter (including
    infant mortality) in Western countries in the
    20th century.
  • Maternal mortality rates of 1 per 100 pregnancies
    (common in the US in 1900) are not rare even now
    in some parts of the world.

12
CONCLUSION 1
  • The perinatal period is a time of such high risk
    to mothers and babies that it is likely that it
    has had great influence on the human genotype

13
A SPECIAL DIFFICULTY OF PERINATAL EPIDEMIOLOGY
SO MUCH IS HIDDEN FROM VIEW
14
HIDDEN DURING PREGNANCY
  • Nearly all of the processes critical to
    competition, adaptation and magnification in
    pregnancy take place where we cannot see them.
    Thus we can only indirectly diagnose fetal
    disease. Often we mistake maternal disease
    manifestations (which we can see) for fetal
    disease (which we cannot see), or measurable
    fetal effects, such as birthweight, for subtler
    processes in the mother/placenta that influence
    birthweight.

15
HIDDEN IN INFANCY
  • Even after birth, the infant often cannot
    provide direct information about disease
    manifestations, and the rapid rate of change in
    the fetus/infant further impairs ability to
    diagnose.
  • For example, we cannot directly diagnose
    neurodevelopmental disorders until the function
    of interest is capable of manifestation. This is
    why cerebral palsy and mental retardation cannot
    be diagnosed in infancy.

16
CONCLUSION 2
  • Because so much is hidden from view in perinatal
    epidemiology, confounding is much more difficult
    to detect than in other epidemiologic fields.

17
WHAT DO I MEAN BY THE TWO FACES OF PERINATAL
EPIDEMIOLOGY?
  • The main thing I mean by this term is that
    unlike most of epidemiology which has two poles
    exposure and outcome, the perinatal period is
    both an exposure and an outcome, at times facing
    backwards towards the mother and her history, at
    times facing forward to the child and its future
    development.

18
BUT THERE ARE OTHER DICHOTOMIES NOT SEEN IN OTHER
TYPES OF EPIDEMIOLOGY
  • Fetus and the newborn In a few seconds, the
    newborn achieves independent existence after
    spending nine months tied to his or her mothers
    blood supply for food and oxygen
  • Placenta and fetus The embryo divides into two
    parts and the placenta then becomes an essential
    support system for the baby. But sometimes the
    support system interferes with fetal development
  • A baby and its twin Twins and other multiples
    have their own unique and complicated
    interactions (e.g. t-t transfusion, freemartins)

19
THE MOST IMPORTANT DICHOTOMY
  • COMPETITION BETWEEN MOTHER AND CHILD

20
CONCLUSION 3
  • For each set of genes that have evolved because
    of perinatal pressures, one must consider whether
    they are designed for optimal fetal or for
    optimal maternal survival, which may be in
    competition.

21
THESE IDEAS LEAD ME TO RAISE A FUNDAMENTAL
QUESTION
  • IS THE FETAL ORIGINS HYPOTHESIS POSSIBLY A
    MATERNAL ORIGINS HYPOTHESIS?

22
THRIFTY GENOTYPE
  • The concept that we have genes that have evolved
    to make the maximum use of foodstuffs. We thus
    are genetically programmed to gain weight, retain
    fats, and thus be at risk for diabetes and
    cardiovascular disease under conditions of food
    abundance. Concept first proposed in 1962 by
    James Neel of the University of Michigan.
  • Neel JV Diabetes mellitus a "thrifty"
    genotype rendered detrimental by "progress"?Am J
    Hum Genet. 1962 Dec14353-62

23
THRIFTY PHENOTYPE
  • The concept that fetal malnutrition sets in
    motion processes that create fetal nutritional
    thrift which in turn lead to higher rates of CVD
    in later life. Concept proposed by Hales and
    Barker in 1992. It is another name for the
    fetal origins hypothesis
  • Hales CN, Barker DJ Diabetologia.
    199235595-601

24
THRIFTY GENOTYPE? THRIFTY PHENOTYPE?
  • OR
  • THE NIFTY, SHIFTY MATERNOTYPE?

25
NIFTY SHIFTY MATERNOTYPE
  • To maximize a successful maternal and fetal
    outcome of pregnancy, the mother develops several
    components of the cardiovascular risk state.
  • I hypothesize that genes that predispose to
    cardiovascular disease originated as genes
    designed either to facilitate the shift of
    resources from mother to fetus/infant during
    pregnancy and lactation or to facilitate optimum
    survival of the mother.

26
WHY SHIFTY AND NIFTY?
  • SHIFTY MATERNOTYPE a genotype rich in genes
    that promote the shift of nutrients from mother
    to baby
  • NIFTY MATERNOTYPE a genotype rich in genes that
    promote maternal survival
  • Both genotypes can predispose to cardiovascular
    disease, but by different mechanisms

27
FETAL ORIGINS
  • A corollary of this hypothesis is that some of
    the fetal phenotypes that have been linked to
    adult cardiovascular risk may in fact reflect
    maternal genotypes, seen in the fetus either
    because of shared genetic heritage with their
    mothers, or because of the consequences of the
    maternal genotype on fetal development.

28
TYPICAL CARDIOVASCULAR RISK FACTORS
  • Increased body mass index
  • Increased fat deposition
  • Hyperlipemia, hypertriglyceridemia
  • Hyperinsulinism and insulin resistance
  • Tendency to thrombophilia

29
THE PREGNANT STATE (ESPECIALLY THIRD TRIMESTER)
  • WEIGHT Increase in BMI and fat deposition
  • LIPIDS increases in all lipid fractions,
    especially triglycerides
  • INSULIN Massive increase in insulin secretion
    and corresponding increase in insulin resistance
    and propensity to diabetes
  • COAGULATION Dominance of pro-coagulant state (?
    thrombin, PAI, thromboxane, factors VII, VIII, X,
    and greatly enhanced risk of thrombotic disorders)

30
FAR OR PSEUDOPREGNANT?
  • The metabolic syndrome or syndrome X the
    clustering of hypertension, hyptriglyceridemia,
    hyperinsulinemia, fat deposition and hyperlipemia
    is in some sense a partial replication of the
    pregnant state.

31
EXAMPLE OF A SHIFTY MATERNOTYPE AFFECTING INFANT
CVD RISK
  • Infants of diabetic mothers are
    characteristically large at birth. Maternal
    processes have been very successful in
    transferring calories to the fetus. Such children
    appear to be at higher risk of obesity and Type
    II diabetes. Some populations, such as Pima
    Indians, are notable for big babies and high risk
    of type 2 diabetes.

32
EXAMPLE OF A NIFTY MATERNOTYPE AFFECTING CVD RISK
  • The intense pro-coagulant maternal state in
    pregnancy might promote placental clots that
    interfere with fetal perfusion and produce
    impaired fetal growth. The maternal genes
    promoting coagulation are passed on to the fetus
    for whom they promote CVD risk (as they do in the
    mother). This gives the impression that impaired
    fetal growth leads to CVD.

33
PRE-ECLAMPSIA
  • Pre-eclampsia may be a maternal response to the
    fetal drive to obtain more nutrients the
    originary lesion appears to be failure of
    placental trophoblast to convert spiral arteries
    into vasoconstrictor-resistant low pressure high
    flow conduits. This may be an extreme
    illustration of a maternal protective (nifty)
    gene, and it is likely to be found in populations
    with low birthweight and hypertension, the latter
    from an excess of genes promoting
    vasoconstriction.

34
BIRTHWEIGHT
  • High birthweights in a population (except perhaps
    in cold climates where infant fat is critical to
    survival) likely represents the shifty
    maternotype, while low birthweight populations
    might represent nifty maternotypes, sacrificing
    fetal growth for maternal survival.
  • Populations with high birthweight might suffer
    especially from diabetes with low birthweight,
    especially from hypertension.

35
FINAL THOUGHTS
  • Perinatal epidemiology is a very rich and
    exciting field of research with profound
    implications for human health
  • It is a relatively small field, and greatly in
    need of young investigators
  • New ways of looking at the interactions of
    mothers, babies and placentas open up exciting
    avenues of research
Write a Comment
User Comments (0)
About PowerShow.com