Jump to: Page Content, Site Navigation, Site Search,
You are seeing this message because your web browser does not support basic web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.
Dorthe Hansen a John
F Kennedy Institute, Gl Landevej 7, 2600 Glostrup, Denmark, b Centre for
Research in Health and Social Statistics, Danish National Research
Foundation, Sejrøgade 11, 2100 Copenhagen Ø, Denmark, c Danish Epidemiology Science
Centre, Vennelyst Boulevard 6, 8000 Aarhus C, Denmark
Correspondence to: Dr Hansen
d209325{at}inet.uni2.dk
Exposure to smog, floods,1 or
earthquakes2 has been associated with a lower sex ratio
(proportion of males) in offspring conceived at the time of the
exposure episode. We hypothesised that exposure to severe life events
before and during the periconceptional period might be associated with
a decline in the sex ratio.
All Danish women who gave birth from 1 January 1980 to 31 December 1992 were identified by the population based medical birth registry. By linking personal identification numbers to the Danish statistical office's fertility database, we identified all the women's partners and older children. A partner was defined as the
father of the child or the partner with whom the woman was cohabiting
on 1 January in the year of birth. Severe life events were defined as
death or admission to hospital for cancer (codes 140 to 209 (excluding
208 polycythemia vera) of the international classification of diseases,
eighth revision) or acute myocardial infarction (code 410) in the
partner or older children. By linking the personal identification
numbers to the mortality registry and to the national registry of
patients, we identified all deaths and all admissions to hospital of
partners and children between 1978 and 1992.
![]()
Methods and results
Top
Methods and results
Comment
References
We identified all women exposed to severe life events in the year of birth and the previous year but included only the women exposed before the second trimester. Women with diabetic partners were excluded, as it has been reported that the sex ratio in their offspring is higher. The time of exposure was recorded as the date of death or first admission to hospital. Information on the possible confounding variables was obtained from the registries.
The exposed cohort consisted of 3072 singleton pregnancies exposed to severe life events and a control cohort of 20 337 singleton pregnancies randomly selected among all pregnancies without such exposure in the observation period. Of all the offspring, 945 had congenital malformations, chromosomal abnormalities, or hereditary diseases.
Using logistic regression analysis, we found that the proportion of boys was 49.0% in the exposed group and 51.2% the control group, giving a crude overall lower ratio between the two sex odds (sex odds ratio) of 0.92 and an adjusted ratio of 0.91 (95% confidence interval 0.84 to 0.99) (table). Exclusion of offspring whose mothers were exposed during the first trimester and all offspring with congenital malformations gave similar results (data not shown).
The nearer the exposure was to conception, the lower the overall sex
odds ratio (test for trend P=0.013) and the lower the sex ratio for
exposure by an older sibling only (P=0.035) and for exposure by death
of a partner only (P=0.016).
| |
Comment |
|---|
|
|
|---|
The results show that severe life events may reduce the sex ratio, especially for exposures around the time of conception, because of differential conception or differential abortion of male embryos. The study cohort was large, and the registration of death, cancer, and the offsprings' sex is known to be accurate and complete in the registers used. The results are consistent with results for natural disasters. 1 2
The study has some limitations. The exact dates of the actual stress
exposure may in most cases have started long before our date of
exposure. For this reason, we also included women exposed during the
first trimester. More factors may have contributed to a dilution of the
effect
for example, other stressors may have affected both the women
in the exposed group and those in the control group, and the partners
may not have been the father of the offspring in all cases.
Psychological stress related to severe life events may alter the sex
ratio through changes in sexual activity, changes in hormones around
the time of conception,3 reduced semen
quality,
2 4
or an increased rate of early male
abortion.5
| |
Acknowledgments |
|---|
DH and JO also work, as paediatrician and professor respectively, at the Danish Epidemiology Science Centre, Statens Serum Institut, in Copenhagen.
Contributors: DH and JO contributed to the idea, design, analysis, interpretation of data, and writing of the paper. HM contributed to the interpretation of the data and critically reviewed the draft paper. All authors will act as guarantors for the paper.
| |
Footnotes |
|---|
Funding: Danish Medical Research Council, Health Insurance Foundation, Dagmar Marshall Foundation, and Danish Medical Association Research Foundation. The activities of the Danish Epidemiology Science Centre are financed by a grant from the Danish National Research Foundation.
Competing interests: None declared.
| |
References |
|---|
|
|
|---|
| 1. | Lyster WR. Altered sex ratio after London smog of 1952 and the Brisbane flood of 1965. J Obstet Gynecol Br Commonwealth 1974; 81: 626-631. [Medline] |
| 2. |
Fukuda M, Fukuda K, Shimizu T, Møller H.
Decline in sex ratio at birth after Kobe earthquake.
Human Reprod
1998;
13:
2321-2322 |
| 3. | James WH. Evidence that mammalian sex ratios at birth are partially controlled by parental hormones levels at the time of conception. J Theor Biol 1996; 180: 271-286[Medline]. |
| 4. |
Fenster L, Katz DF, Wyrobek AJ, Pieper C, Rempel DM, Oman D, et al.
Effects of psychological stress on human semen quality.
J Androl
1997;
18:
194-202 |
| 5. | Pratt NC, Lisk RD. Effects of social stress during early pregnancy on litter size and sex ratio in the golden hamster (Mesocricetus auratus). J Reprod Fert 1989; 87: 736-769. |
(Accepted 31 March 1999)
Read all Rapid Responses