NSIDRC Journal Article Alert — June 6, 2008
Prepared by the National Sudden Infant Death Resource Center
at Georgetown University.
This journal article alert provides selected items added to
the National Library of Medicine’s PubMed database in
the last week.
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Sudden Infant Death
1. Mitchell EA, Thompson JM, Becroft
DM, Bajanowski T, Brinkmann B, Happe A, Jorch G, Blair PS,
Sauerland C, Vennemann MM
Head covering and the risk for SIDS: findings from the New
Zealand and German SIDS case-control studies
Pediatrics. 2008 Jun;121(6):e1478-83
University of Auckland, Department of Paediatrics, Private
Bag 92019, Auckland, New Zealand. e.mitchell@auckland.ac.nz
OBJECTIVES: The aim of this investigation was to identify
risk factors for being found with the head covered in sudden
infant death syndrome cases and determine whether head covering
was likely to be an agonal event or potentially part of the
causal pathway in some cases. By using the data from 2 sudden
infant death syndrome case-control studies, consistency of
the findings could be assessed. METHODS: Two case-control studies
were assessed: (1) the New Zealand Cot Death Study (1987-1990,
393 sudden infant death syndrome cases) and (2) a German SIDS
case-control study (1998-2001, 333 sudden infant death syndrome
cases). RESULTS: The proportion of sudden infant death syndrome
cases in which infants were found with their head covered was
15.6% in the New Zealand study and 28.1% in the German study.
Being found with head covering was associated with older infant
age. In both studies, being found with head covering was associated
with being very sweaty when found. Head covering was also associated
with the incidence and severity of thymic petechiae in both
studies. Both the position in which the child was placed to
sleep and the position in which the child was found were not
associated with head covering. CONCLUSIONS: The finding that
sudden infant death syndrome cases in which infants were found
with their heads covered were often very sweaty suggests that
head covering was not an agonal event and that it preceded
the death and may have been causally related to the death.
Infants who were found with their head covered were older,
which probably reflects motor development.
Other Infant Death
1. Weber M, Klein Nj, Hartley J, Lock P, Malone M, Sebire
Nj
Infection and sudden unexpected death in infancy: a systematic
retrospective case review
Lancet. 2008 May 31;371(9627):1848-53
Department of Paediatric Pathology, Great Ormond Street Hospital
for Children and the Institute of Child Health, University
College London, London, UK.
BACKGROUND: The cause and mechanism of most cases of sudden
unexpected death in infancy (SUDI) remain unknown, despite
specialist autopsy examination. We reviewed autopsy results
to determine whether infection was a cause of SUDI. METHODS:
We did a systematic retrospective case review of autopsies,
done at one specialist centre between 1996 and 2005, of 546
infants (aged 7-365 days) who died suddenly and unexpectedly.
Cases of SUDI were categorised as unexplained, explained with
histological evidence of bacterial infection, or explained
by non-infective causes. Microbial isolates gathered at autopsy
were classified as non-pathogens, group 1 pathogens (organisms
usually associated with an identifiable focus of infection),
or group 2 pathogens (organisms known to cause septicaemia
without an obvious focus of infection). FINDINGS: Of 546 SUDI
cases, 39 autopsies were excluded because of viral or pneumocystis
infection or secondary bacterial infection after initial collapse
and resuscitation. Bacteriological sampling was done in 470
(93%) of the remaining 507 autopsies. 2079 bacteriological
samples were taken, of which 571 (27%) were sterile. Positive
cultures yielded 2871 separate isolates, 484 (32%) of which
showed pure growth and 1024 (68%) mixed growth. Significantly
more isolates from infants whose deaths were explained by bacterial
infection (78/322, 24%) and from those whose death was unexplained
(440/2306, 19%) contained group 2 pathogens than did those
from infants whose death was explained by a non-infective cause
(27/243, 11%; difference 13.1%, 95% CI 6.9-19.2, p<0.0001
vs bacterial infection; and 8.0%, 3.2-11.8, p=0.001 vs unexplained).
Significantly more cultures from infants whose deaths were
unexplained contained Staphylococcus aureus (262/1628, 16%)
or Escherichia coli (93/1628; 6%) than did those from infants
whose deaths were of non-infective cause (S aureus: 19/211,
9%; difference 7.1%, 95% CI 2.2-10.8, p=0.005; E coli: 3/211,
1%, difference 4.3%, 1.5-5.9, p=0.003). INTERPRETATION: Although
many post-mortem bacteriological cultures in SUDI yield organisms,
most seem to be unrelated to the cause of death. The high rate
of detection of group 2 pathogens, particularly S aureus and
E coli, in otherwise unexplained cases of SUDI suggests that
these bacteria could be associated with this condition. FUNDING:
Foundation for the Study of Infant Deaths.
2. Kung HC, Hoyert DL, Xu J, Murphy SL
Deaths: final data for 2005
Natl Vital Stat Rep. 2008 Apr 24;56(10):1-120
Division of Vital Statistics, U.S. Department of Health and
Human Services, National Center for Health Statistics, Centers
for Disease Control and Prevention, Hyattsville, MD 20782,
USA
OBJECTIVES: This report presents final 2005 data on U.S. deaths,
death rates, life expectancy, infant and maternal mortality,
and trends by selected characteristics such as age, sex, Hispanic
origin, race, marital status, educational attainment, injury
at work, state of residence, and cause of death. METHODS: This
report presents descriptive tabulations of information reported
on death certificates, which are completed by funeral directors,
attending physicians, medical examiners, and coroners. The
original records are filed in the state registration offices.
Statistical information is compiled into a national database
through the Vital Statistics Cooperative Program of the Centers
for Disease Control and Prevention's National Center for Health
Statistics (NCHS). Causes of death are processed in accordance
with the International Classification of Diseases, Tenth Revision
(ICD-10). RESULTS: In 2005, a total of 2,448,017 deaths were
reported in the United States. The age-adjusted death rate
was 798.8 deaths per 100,000 standard population, representing
a decrease of 0.2 percent from the 2004 rate and a record low
historical figure. Life expectancy at birth remained the same
as that in 2004-77.8 years. Age-specific death rates decreased
for the age group 65-74 years but increased for the age groups
15-24 years, 25-34 years, and 45-54 years. The 15 leading causes
of death in 2005 remained the same as in 2004. Heart disease
and cancer continued to be the leading and second leading causes
of death, together accounting for almost one-half of all deaths.
The infant mortality rate in 2005 was 6.87 deaths per 1,000
live births. CONCLUSIONS: Generally, mortality patterns in
2005, such as the age-adjusted death rate declining to a record
historical low, were consistent with long-term trends. Life
expectancy in 2005 remained the same as that in 2004.
Bereavement
1. Surkan PJ, Rådestad I, Cnattingius S, Steineck G,
Dickman PW
Events after stillbirth in relation to maternal depressive
symptoms: a brief report
Birth. 2008 Jun;35(2):153-7
Division of Clinical Cancer Epidemiology, Department of Oncology
and Pathology, Karolinska Institutet, Stockholm, Sweden
BACKGROUND: Actions taken after a stillbirth can affect long-term
psychological morbidity. Our objective was to study how infant
bonding and maternal actions after stillbirth are associated
with ensuing depressive symptoms. METHODS: Using the population-based
Swedish Medical Birth Register, we identified all 380 Swedish-speaking
women who gave birth to singleton stillborn infants in Sweden
in 1991. Of these, 314 (83%) completed a postal questionnaire
3 years after the stillbirth. Items included actions taken
to bond with the baby and demographics. The association between
care-related factors and later maternal depressive symptoms
was quantified using relative risks estimated using multivariable
regression. RESULTS: We observed an almost sevenfold increased
risk of depressive symptoms for mothers who reported not being
with their babies as long as they wished (adjusted risk ratio
[RR] 6.9, 95% CI 2.4-19.8). Compared with women who became
pregnant again within 6 months, those with no later pregnancy
were at higher risk of depressive symptoms (adjusted RR 2.8,
95% CI 0.9-8.4). In addition, compared with women who experienced
a stillbirth in their first pregnancy, stillbirth occurring
with an infant who was third in the birth order was related
to a twofold risk of elevated depressive symptoms (adjusted
RR 2.2, 95% CI 0.8-6.4). Furthermore, stillbirth occurring
in a fourth or later pregnancy was associated with an almost
sevenfold risk of depressive symptomatology (adjusted RR 6.7,
95% CI 2.2-20.5). No evidence of an association was found between
other care-related actions and subsequent maternal depressive
symptoms. CONCLUSIONS: Our results suggest that a mother being
with the stillborn baby for as long as desired and the birth
order of the stillbirth may influence her later depressive
symptomatology. Compared with mothers who became pregnant again
within 6 months, those who did not have a subsequent pregnancy
were at higher risk of depressive symptoms at 3 years' follow-up.
2. McCreight BS
Perinatal loss: a qualitative study in Northern Ireland
Omega (Westport). 2008;57(1):1-19
University of Ulster, School of Sociology and Applied Social
Studies, Northern Ireland. bs.mccreight@ulster.ac.uk
This article describes the experiences of women in Northern
Ireland who have experienced a miscarriage or stillbirth. Pregnancy
loss encompasses several dimensions of loss for women, loss
of the future, loss of self-identity, and the loss of anticipated
parenthood. The study explored how women emotionally responded
to loss and the care they received from medical staff. Burial
arrangements for the remains of the baby are also explored.
The methodology adopted a narrative approach based upon in-depth
interviews with 23 women who attended pregnancy loss self-help
groups. The women's narratives highlight their emotional responses
to loss, the medicalization of perinatal grief, and burial
arrangements. Women felt that their experience was emotionally
negative in that they had been subjected to a rationalizing
process of medicalization. The primary focus for the women
was on the need to recover space for their emotions and seek
acceptance and recognition of the validity of their grief.
The study demonstrated that the women's response to being marginalized
led them to make sense of their experiences and to create spaces
of resistance to medicalization. The way in which women placed
emotion at the center of their narratives is taken to be a
powerful indicator that the support they require from professionals
should take account of the meanings they have constructed from
their experience of loss.
Miscarriage/Stillbirth/Prenatal Issues
1. Das S, Ankola P, Chiechi M, Sandhu J
Perinatal Cerebral Arterial Infarction Associated with a Placental
Chorioangioma
Am J Perinatol. 2008 Jun 2. [Epub ahead of print]
Department of Pediatrics, Metropolitan Hospital Center, New
York Medical College, New York, New York
Placental chorioangiomas are benign vascular tumors. Large
chorioangiomas cause several obstetric complications, including
premature labor, placental abruption, polyhydramnios, fetal
hydrops, fetal growth restriction, fetal hepatosplenomegaly,
cardiomegaly, congestive heart failure, and fetal death. The
neonatal complications are hydrops fetalis, microangiopathic
hemolytic anemia, and thrombocytopenia. The cause of perinatal
cerebral arterial infarction remains unclear in the majority
of cases. Investigators have reported a number of obstetric
and neonatal complications in the setting of perinatal stroke,
including birth asphyxia, preeclampsia, chorioamnionitis, cardiac
anomalies, polycythemia, systemic infection, and genetic thrombophilias.
We present a rare case of perinatal cerebral infarction associated
with placental chorioangioma.
2. Salihu HM, Alio AP, Wilson RE, Sharma PP, Kirby RS, Alexander
GR
Obesity and Extreme Obesity: New Insights Into the Black-White
Disparity in Neonatal Mortality
Obstet Gynecol. 2008 Jun;111(6):1410-1416
Departments of Epidemiology and Biostatistics, Obstetrics
and Gynecology, Community and Family Health, and Pediatrics,
University of South Florida, Tampa, Florida; the Department
of Epidemiology, UMDNJ-School of Public Health, New Brunswick,
New Jersey; and the Department of Maternal and Child Health,
University of Alabama at Birmingham, Birmingham, Alabama.
OBJECTIVE: To estimate whether the preponderance of obesity
among black women could explain the black-white disparity in
neonatal mortality. METHODS: This is a population-based study
using longitudinally collected data among pregnant women from
the state of Missouri spanning almost two decades (1978-1997).
Obesity is defined in this study as body mass index (BMI) of
at least 30 and further categorized into the typically reported
three subclasses: class I (BMI 30.0-34.9), class II (BMI 35.0-39.9),
and extreme/morbid obesity (BMI at least 40). The main outcome
measures were neonatal mortality, early neonatal mortality,
and late neonatal mortality. RESULTS: Overall, neonatal mortality
and early neonatal mortality but not late neonatal mortality
increased with higher obesity subclass, with the greatest risk
registered among morbidly obese mothers (hazards ratio for
neonatal mortality 1.3; 95% confidence interval [CI] 1.1-1.5;
hazards ratio for early neonatal mortality 1.3; 95% CI 1.1-1.5).
Among blacks, the risk for neonatal, early, and late neonatal
mortality increased significantly with rising BMI (50-100%
increments). However, offspring of obese white mothers had
no elevated risks for any of the three indices of mortality
regardless of maternal obesity subclass. CONCLUSION: Neonates
of obese black mothers have an elevated risk of mortality throughout
the neonatal period, whereas those of obese white mothers do
not. Obesity among black mothers may contribute to the persistent
black-white disparity in infant survival in the United States
and could provide an avenue for narrowing the black-white gap
in infant mortality. LEVEL OF EVIDENCE: II.
3. Tokyol C, Aktepe F, Husniye Dilek F, Yilmazer M
Comparison of Placental PTEN and beta1 Integrin Expression
in Early Spontaneous Abortion, Early and Late Normal Pregnancy
Ups J Med Sci. 2008;113(2):235-42
Departments of Pathology, Afyon Kocatepe University School
of Medicine, Afyonkarahisar, Turkey
Background: PTEN seems to play an important role in cell cycle,
growth, migration, and death. Integrins are cell surface receptors
that play a role in the regulation of cell proliferation, differentiation,
implantation, and embryogenesis. PTEN inhibits 1 integrin signaling.
The objective of this study is to investigate the expression
of PTEN and 1 integrin in placental tissues of early spontaneous
abortion and first and third trimesters of normal pregnancy.Method:
A total of 43 placental tissue samples were evaluated using
immunohistochemistry for PTEN and 1 integrin. Group 1 included
placental tissues of volunteer termination of normal pregnancy
during the first trimester (5-10 wk gestation). Group 2 included
placental tissues of normal vaginal delivery at the third trimester
of pregnancy (36-40 wk gestation). Group 3 included placental
tissues of pregnancy termination because of spontaneous abortion
during the first trimester (5-10 wk gestation). Results: PTEN
expression of villous trophoblast was decreasing as the pregnancy
advanced. PTEN staining of decidual cells was significantly
stronger in tissue samples from early spontaneous abortion
than in tissue samples from early and late normal pregnancy
(p=0.003, p=0.001, respectively). There was no significant
difference between 1 integrin expression of villous trophoblast
and decidual cells in three groups.Conclusion: Our findings
suggest that altered patterns of PTEN expression may be associated
with abortion, but it seems that 1 integrin does not contribute
to this process as a signaling protein. Further evaluation
is needed to highlight this subject.
4. Moreau P, Contu L, Alba F, Lai S, Simoes R, Orrù S,
Carcassi C, Roger M, Rabreau M, Carosella ED
HLA-G Gene Polymorphism in Human Placentas: Possible Association
of G*0106 Allele with Preeclampsia and Miscarriage
Biol Reprod. 2008 May 28 [Epub ahead of print]
Definite causes for several pregnancy pathologies remain unknown.
However, in the light of different recent studies, it is notable
that diminished or aberrant HLA-G expression may be associated
with certain complication of pregnancy, and may be further
link to HLA-G polymorphism. We analysed DNA from 60 normal
placentas (controls), 140 placentas from miscarriage, 36 pre-eclamptic
placentas, 76 placentas from fetal hypotrophy and 34 placentas
with hypoxia, for variations in coding regions (allelic groups
G*0101 to G*0107), and the 14 bp deletion/insertion into the
3'UT region. No statistically significant differences were
observed in the distribution of allelic group between pathological
placentas and controls with the exception of G*0106 allele
frequency in pre-eclampsia compared with control placentas
(21.2 % and 6.6 % respectively). A greater frequency of this
allele also was observed in two subgroups of miscarriage and
hypoxia pathologies than in the controls. In addition, the
presence of the 14 bp sequence was prominent in pre-eclampsia
compared with control (60.8 % versus 35 %) and homozygotes
with deletion were not detected in the pathology. The results
suggest that G*0106 allele which is coupled with the presence
of 14 bp contribute and/or is a relevant marker in some specific
pregnancy complications, especially pre-eclampsia.
5. Bartholin L, Melhuish TA, Powers SE, Goddard-Léon
S, Treilleux I, Sutherland AE, Wotton D
Maternal Tgif is required for vascularization of the embryonic
placenta
Dev Biol. 2008 May 2. [Epub ahead of print]
Department of Biochemistry and Molecular Genetics, University
of Virginia, USA; Center for Cell Signaling, University of
Virginia, USA
The mammalian placenta is the site of exchange of nutrients
and waste between mother and embryo. In humans, placental insufficiency
can result in intrauterine growth retardation, perinatal death
and spontaneous abortion. We show that in C57BL/6J mice a null
mutation in the gene encoding the transcriptional corepressor,
Tgif, causes placental defects. The major defects are decreased
vascularization of the placenta, due to a decrease in the fetal
blood vessels, and decreased expression of the gap junction
protein Gjb2 (Cx26). These defects result in severe growth
retardation in a proportion of Tgif null embryos in Tgif heterozygous
mothers, and an overall growth delay in Tgif null animals.
Placental defects are much more severe if the mother also completely
lacks Tgif function, and placentas from heterozygous Tgif embryos
are defective in a Tgif null mother. Embryo transfer experiments
show that even the placenta from a wild type embryo is compromised
in the absence of maternal Tgif. These results demonstrate
that Tgif functions in the normal development of the placenta,
and suggest a role for maternal factors in regulating the morphogenesis
of embryonically-derived placental tissues.
6. Fellman J, Eriksson AW
Correlations between live and stillbirth outcomes in twin pairs
Hum Biol. 2008 Feb;80(1):29-40
Folkhälsan Institute of Genetics, Department of Genetic
Epidemiology, PO Box 211, Fin-00251 Helsinki, Finland.
A relationship has been proposed to exist between individual
outcomes (live or stillbirth) of twins in the same set. Here,
we analyze this association between live births and stillbirths
among individuals in different twin pairs. When national birth
registers are analyzed, individuals in opposite-sex twin sets
can be identified and the correlation between individual outcomes
estimated. However, full information about the individuals
in same-sex twin sets is not, as a rule, available, and consequently,
correlation coefficients cannot be estimated, but upper and
lower limits of the correlation coefficients can be obtained.
The methods introduced here were applied to data from Sweden
(1869-1967), the Aland Islands (Finland) (1750-1949), the Kingdom
of Saxony (1881-1900), and England and Wales (1940-2003). Comparisons
between the correlation coefficients among opposite-sex twins
and the lower bound (minimum) of correlation coefficients among
same-sex twins indicate that in all populations studied a stronger
association exists between twins in same-sex rather than opposite-sex
twin sets or pairs. For opposite-sex twin sets no general association
between the correlation coefficient and the stillbirth rate
was identified.
Prepared by the
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