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.
Abstract

Related Concept Videos

Pedigree Analysis01:35

Pedigree Analysis

Overview
Sex-linked Disorders01:43

Sex-linked Disorders

Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
Nondisjunction01:21

Nondisjunction

Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers.  Nondisjunction is common during anaphase I or anaphase II of meiosis.  Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold sister...
Autoimmune Disorders01:29

Autoimmune Disorders

Autoimmune diseases are a group of disorders in which the body's immune system mistakenly attacks its own cells, tissues, and organs. This results from an overactive immune response against substances and tissues normally present in the body. Let's delve into the concept and mechanism of autoimmune diseases from an immune system point of view, explore different causes and examples of such diseases, and discuss potential solutions.
Concept and Mechanism of Autoimmune Diseases
The immune system...