Leading scientists have identified an important gene that is associated with cleft lip and palate. Experts say the discovery is a step closer to understanding how this birth defect arises, and will help in the development of medical approaches to prevent the disfiguring condition.
An international team, led by Newcastle University, UK, and the University of Bonn in Germany, has found that variants near a gene called GREM1 (Gremlin1) significantly increase the risk for cleft lip and palate.
A cleft is a gap in the upper lip, the roof of the mouth, or sometimes both. Each year, approximately 250,000 babies worldwide are born with a cleft, equating to about two babies a day in the UK.
Dr Heiko Peters, who works at Newcastle University’s Institute of Genetic Medicine, is senior author of the research paper published in the journal, PLoS Genetics.
He said: “The findings reveal a link between GREM1 and specific clinical characteristics that arise in the formation of a cleft lip and palate.
“This is very important in this research area as it helps to decipher the complex interplay between genes required for the different steps and in different tissues during lip and palate development.
“A cleft lip can occur with or without a cleft palate and the genetic factors that predispose to palate involvement are largely unknown.”
The research team carried out analyses on genetic and clinical data from three large patient cohorts and identified a strong association between a region on chromosome 15 and cleft lip and palate.
Experts carried out studies on mice to investigate where GREM1 is normally active in the development of the face and how alterations in the gene’s activity may affect the lip and palate.
Results indicate that it is not the loss of GREM1 function but rather its increased activity that causes the condition.
It is the second gene which has been shown to be linked to a condition in which a cleft of the lip and a cleft of the secondary palate occur together.
Dr Peters added: “These findings provide a framework for further analyses of GREM1 in human cell systems and model organisms, broadening our understanding of the processes that regulate the face’s shape.”
Although not life-threatening for patients with access to postnatal surgery, cleft lip and palate requires additional multidisciplinary care by specialists, including ear, nose and throat experts, orthodontists and speech therapists.
Children with the condition can have dental issues, speech problems and are at increased risk of serious ear infections and hearing loss.
Currently, scientists only have a fragmented picture about which genes are required for lip and palate development, and how environmental factors might interact with genetic risk factors.
To establish effective prevention strategies scientists must identify genetic risk factors and understand how gene-gene and gene-environment interactions interfere with lip and palate development.
As the use of personalized medicine increases, understanding how genetic changes alter fetal development will become increasingly relevant.
This is particularly important for conditions such as cleft lip and palate that appear to be caused by a combination of genetic and environmental factors, such as smoking or certain medicines used by the mother.
Further studies will focus on identifying genes and environmental factors that interact with GREM1.
Dr Laura Yates, consultant in clinical genetics at Newcastle upon Tyne Hospitals NHS Foundation Trust, said: “The families we meet in genetic clinics on a daily basis generally have two common questions.
“Firstly, what is the cause of the developmental anomaly affecting their child or themselves, and secondly, can it be treated or prevented in future pregnancies?
“Studies such as this contribute vital pieces of information that enable clinicians to provide patients with answers that are relevant to them and their family, not just general statistics.
“Our understanding of how genetic factors in both mother and fetus, and external or environmental influences impact on fetal development in the womb, is far from complete.
“This study takes us one step closer to being able to identify genetic changes that increase the chance of a particular form of cleft lip and palate re-occurring in a family, therefore to studying what can be done to reduce the chance of this happening in individuals who have this genetic change.”
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