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Possible Cause For SIDS Identified In Groundbreaking Study
Home>News
Updated 13:02 24 May 2024 GMT+1Published 16:15 13 May 2022 GMT+1

Possible Cause For SIDS Identified In Groundbreaking Study

A scientific study has just discovered a potential reason behind sudden infant death syndrome.

Rhiannon Ingle

Rhiannon Ingle

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Featured Image Credit: Alamy/Shutterstock

Topics: News, No Article Matching

Rhiannon Ingle
Rhiannon Ingle

Rhiannon Ingle is a Senior Journalist at Tyla, specialising in TV, film, travel, and culture. A graduate of the University of Manchester with a degree in English Literature, she honed her editorial skills as the Lifestyle Editor of The Mancunian, the UK’s largest student newspaper. With a keen eye for storytelling, Rhiannon brings fresh perspectives to her writing, blending critical insight with an engaging style. Her work captures the intersection of entertainment and real-world experiences.

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Trigger Warning: This article discusses baby loss

Sudden infant death syndrome, also commonly known as SIDS and sometimes referred to as 'cot death', is the unexplained death of an otherwise completely healthy baby.

According to the National Health Service, it's estimated that approximately 200 babies die every year from SIDS and mostly occurs during an infant's first six months.

A new study points to a direct cause for the tragic syndrome.
Alamy

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The exact cause of the tragic syndrome has been unknown for years, but a new study points to a direct cause.

The Children’s Hospital at Westmead, Australia, has been home to the groundbreaking research that has successfully pinpointed the first-ever biochemical marker that will aid doctors in determining which infants are at a higher risk of SIDS while alive.

It is this biomarker that is deemed to be the key in getting closer to understand the cause of the heart-breaking syndrome.

The research itself in incredibly new, being first published on Sunday (8 May).

The study was published in Lancet’s eBioMedicine.
Alamy

The study was published in Lancet’s eBioMedicine, a leading biomedical open access journal with a core ethos of 'bridging the gap between basic and clinical research'.

The biomarker in question has been revealed to an enzyme called Butyrylcholinesterase, abbreviated to BChE.

Leading the life-changing research is scientist Dr Carmel Harrington, whose own baby died due to SIDS nearly 30 years ago, making this a particularly relevant area of study.

Leading the life-changing research is scientist Dr Carmel Harrington.
Alamy

Following a study investigating the varying activity in a sample of 722 Dried Blood Spots taken at the point of birth, scientists measured this BChE biomarker levels at birth and made a breakthrough discovery.

The study found that the levels of BChE were dramatically lower in the infants that went on to die from SIDS, when compared inline with the biomarker levels in babies who later died of other causes or who went on to live.

From this, the scientists were able to draw the conclusion that an 'arousal deficit' is what can make infants more vulnerable to SIDS.

The lead doctor has since dubbed the groundbreaking study as "game changing".
Alamy

They found that this is because BChE is a large factor involved in the brain’s 'arousal pathway’.

Dr Harrington said: "This has long been thought to be the case, but up to now, we didn’t know what was causing the lack of arousal. Now that we know that BChE is involved we can begin to change the outcome for these babies and make SIDS a thing of the past.”

The lead doctor has since dubbed the groundbreaking study as 'game-changing', and is positively hopeful for a future in which SIDS is 'a thing of the past'.

If you have suffered the loss of a child, the Baby Loss Awareness Alliance offers resources and support to help you through the process.

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