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Newborn infant characteristics and risk of future rheumatoid arthritis: a twin-control study
Anders J Svendsen1, Kirsten O Kyvik, Gunnar Houen
1The Danish Twin Registry, Epidemiology, Institute of Public Health, University of Southern Denmark, J.B.Winsløwsvej 9B, 5000, Odense C, Denmark, asvendsen@health.sdu.dk.
Insights
Low birth weight does not increase rheumatoid arthritis (RA) risk. However, being the firstborn twin may increase the likelihood of developing RA later in life.
Area of Science:
- Rheumatology
- Epidemiology
- Genetics
Background:
- Low birth weight has been suggested as a potential risk factor for rheumatoid arthritis (RA).
- Twin studies offer a unique approach to disentangle genetic and environmental influences on adult diseases.
- Investigating prenatal factors like birth weight is crucial for understanding RA etiology.
Purpose of the Study:
- To examine the association between birth weight and the development of rheumatoid arthritis (RA).
- To explore the role of birth order as a potential risk factor for RA.
- To leverage a discordant twin-control study design to minimize confounding factors.
Main Methods:
- Utilized a twin-control study design with 42 RA-discordant twin pairs.
- Collected data on birth weight, birth length, and birth order from midwife records.
- Employed difference plots and conditional logistic regression for statistical analysis, adjusting for covariates.
Main Results:
- Birth weight was not found to be significantly associated with the risk of developing RA (OR 1.00).
- The odds of developing RA were higher for firstborn twins compared to their co-twins (OR 2.33).
- These findings remained consistent irrespective of ACPA status.
Conclusions:
- Birth weight is not a significant risk factor for adult rheumatoid arthritis.
- Being the firstborn twin may be associated with an increased predisposition to developing RA.
- Further research is warranted to elucidate the mechanisms behind the birth order-RA association.
Abstract:
Low birth weight has been proposed as a risk factor for rheumatoid arthritis (RA). The twin-control study design provides an opportunity to investigate the significance of potential prenatal determinants for adult morbidity by accounting for maternal characteristics and early environmental and genetic factors. We investigated the association between birth weight and RA in a sample of 42 twin pairs discordant for rheumatoid arthritis in which valid information on birth weight, birth length, and order was available from midwife records. Difference plot and conditional logistic regression were used to investigate the relationship between RA and birth weight or birth order adjusting for birth length and sex. The intra-pairwise birth weight differences, i.e., RA twin minus co-twin, ranged from -750 to 1,100 g, mean 78 g (95 % CI -13 to 70), 146 g (95 % CI (-36 to 329) in monozygotic, 32 g (95 % CI -90 to 154) in dizygotic, same sex and 69 g (95 % CI -122 to 260) in dizygotic, opposite sex twin pairs. The odds ratio for birth weight as risk factor for RA was 1.00 (95 % CI 0.997-1.003) when adjusting for birth length, birth order, and sex, irrespective of ACPA status. The odds ratio for developing RA as first born twin was 2.33 (95 % CI 0.97-5.60) when adjusting for birth length, birth weight, and sex, irrespective of ACPA status. In this twin-control study, birth weight was not associated with the development of RA in adult life. Being born first may predispose to RA.
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