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Birth order and ankylosing spondylitis: no increased risk of developing ankylosing spondylitis among first-born
Sinead Brophy1, Gordon Taylor, Andrei Calin
1Epidemiology Department, Royal National Hospital for Rheumatic Diseases, University of Bath, UK.
Insights
Birth order does not significantly impact ankylosing spondylitis (AS) risk. This study found no increased prevalence of AS in first-born children compared to later-born children.
Area of Science:
- Immunogenetics
- Rheumatology
- Epidemiology
Background:
- Previous studies in HLA-B27 transgenic mice and smaller human cohorts suggested a higher risk of disease in first-born offspring.
- Ankylosing spondylitis (AS) is a chronic inflammatory disease with a known genetic component.
Purpose of the Study:
- To investigate the association between birth order and the risk of developing ankylosing spondylitis (AS) in a large patient cohort.
- To determine if first-born children have a statistically significant higher risk of AS compared to later-born children.
Main Methods:
- Analysis of patient data from the Bath AS database, including 4517 individuals.
- Chi-squared statistical analysis to compare AS prevalence between first-born and later-born children based on their birth order.
Main Results:
- No statistically significant difference in AS prevalence was observed between first-born (36%) and later-born (64%) children (p = 0.295).
- No biological gradient was found, indicating no inverse correlation between birth order and AS risk.
Conclusions:
- The study data does not support a statistically significant effect of birth order on the risk of developing ankylosing spondylitis.
- Potential biases in previous findings may arise from family size and parental disease status, influencing observed birth order effects.
Objective:
In the HLA-B27 transgenic mouse model the first litters have been shown to have a higher percentage of diseased offspring than later litters. First-born children (n = 162) have also been shown to have a higher risk of ankylosing spondylitis (AS) than later-born children. We examined this effect of birth order using similar methods but larger numbers.
Methods:
Patients from the Bath AS database (n = 4517; M:F = 2.5:1) were examined according to position of birth within the family. Chi-squared analysis was used to examine if AS was more prevalent among first-born than later-born children.
Results:
The first-born child was not significantly more likely to have AS than later-born children (p = 0.295). [Observed compared to expected: 1607 (36%) compared to 1641.13 (36%) for first-born children and 2910 (64%) compared to 2876.3 (64%) for later-born children, respectively.] There was no biological gradient (i.e., inverse correlation between birth order and disease risk).
Conclusion:
There was no statistically significant effect of birth order based on our data. Findings suggesting a birth order effect may be skewed, as it is possible that those parents who do have AS will be less likely to have a large family and yet it is their offspring who will be at greatest risk of developing disease. This will affect the data, as those children born into a large family (i.e., high birth order children) will be at a lower risk of AS than any child born into a small but family-history-positive unit.
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