Causes of SIDS
Despite 30 years of research, experts have not yet found an exact cause for SIDS.
Research has shown that some babies who die from SIDS had brain abnormalities that made them more at risk for sudden death during infancy. These studies found abnormalities in the "arcuate nucleus,” the part of the brain that helps control breathing and blood pressure. Babies born with defects in other parts of the brain or body may also be more prone to SIDS. These abnormalities may result from the fetus’ exposure to toxins or decreases in oxygen during pregnancy.
It’s normal for babies to sense when they do not get enough oxygen while sleeping. Their brain triggers them to wake and cry, which changes their heart rate and breathing patterns to increase the amount of oxygen they take in. Babies are at an increased risk for SIDS if they do not inhale enough oxygen or if they inhale too much carbon dioxide.
Some babies affected by SIDS have had an increased number of immune system cells and proteins. These cells and proteins can cause the brain to change the baby’s heart rate and breathing during sleep, or can put the baby into a deeper sleep. Many babies who have died from SIDS have had respiratory infections prior to their deaths. More SIDS cases occur during the colder months of the year, when respiratory and intestinal infections are more common.
Metabolic disorders, such as medium chain acyl-CoA dehydrogenase deficiency, can also put a baby at an increased risk of SIDS. This disorder prevents the baby from processing fatty acids the right way. Over time, a buildup of acid metabolites can lead to issues with breathing and heart function. If there is a family history of metabolic disorders or childhood deaths of unknown cause, genetic screening of the parents can be completed. If one or both parents are found to be a carrier for metabolic disorders, the baby can be tested soon after birth.