Connecting Perinatal Events to Juvenile Idiopathic Arthritis-Uveitis
Connecting Perinatal Events to Juvenile Idiopathic Arthritis-Uveitis
The role of the host microbiota is vital in sustaining immunity. Certain studies have suggested that the production of autoantibodies may underlie the manifestation of JIA. Past research has revealed a strong association between JIA and microbial dysbiosis, particularly reduced levels of specific short-chain-fatty-acid (SCFA)-producing bacteria in the gut, which, in turn, can influence the immune response to microbiota and enhance the circulation of autoantibodies.
Perinatal events, including pregnancy and labor complications, as well as vaginal or cesarean section (CS) deliveries, significantly impact infants' microbial diversity. Unlike vaginal delivery, CS does not facilitate the transfer of maternal microbiota to the child. However, very few studies have explored the connection between perinatal factors and the development of JIA or JIA-uveitis.
The initial hypothesis suggested a higher likelihood of CS delivery for JIA patients due to reduced microbiota diversity. However, the results did not support this hypothesis, emphasizing the need for further research to clarify the impact of CS delivery on JIA.
The study did not establish a significant link between the investigated perinatal events and JIA development. Furthermore, there was no significant association between labor complications, birth routes, and JIA-uveitis. However, the data did reveal a higher incidence of certain complications, such as gestational diabetes (GD), among patients with JIA-uveitis.
These findings could potentially be rationalized by disparities in breastfeeding practices among CS delivery patients. An infant's microbiota diversity can be influenced by the choice of breastfeeding, subsequently affecting autoimmunity. Research indicates that mothers who undergo CS delivery are more likely to experience reduced milk production and delayed lactation onset, limiting beneficial microbe intake by the infant and, in turn, diminishing the stimulation of intestinal flora that plays a role in autoimmune responses and immunity.
Further exploration of these intermediary factors is essential to gain a comprehensive understanding of the observed relationships.
The study sample was relatively homogeneous in terms of composition and size. Therefore, additional research with larger and more diverse sample sizes is required to validate these findings. This study, nonetheless, represents a pioneering effort to systematically assess labor and pregnancy variables and their potential connections with the development of JIA-uveitis and JIA.