Dr. Angela Christiano of Columbia University in New York and a team of scientific researchers have identified a new gene involved in hair growth. Their discovery may affect the direction of future research for hair loss and the diagnosis and ultimate prevention of male pattern baldness.
The condition which leads to thinning hair is called hereditary hypotrichosis simplex. Through the study of families in Pakistan and Italy who suffer from this condition, the team was able to identify a mutation of the APCDD1 gene located in chromosome 18. This chromosome has been linked to other causes of hair loss.
According to Dr. Christiano, “The identification of this gene underlying hereditary hypotrichosis simplex has afforded us an opportunity to gain insight into the process of hair follicle miniaturization, which is most commonly observed in male pattern hair loss or androgenetic alopecia.”
The mutation of the APCDD1 gene inhibits the Wnt signaling pathway. Although this recently discovered gene does not explain the complex process of male pattern baldness, the importance of this discovery lies in the Wnt signaling that the gene directs, has now been shown to control hair growth in humans, as well as in mice.
Reference: Nature 464, 1043-1047 (15 April 2010) | doi:10.1038/nature08875;
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Tags: Androgenetic Alopecia, APCDD1 gene, Causes of Hair Loss, Chromosome 18, Columbia University, Dr. Angela Christiano, Genetic Hair Loss, Hair Follicle, Hair Growth, Hair Loss Genetics News, Hereditary Hypotrichosis Simplex, Male Pattern Baldness, Male Pattern Hair Loss, Miniaturization, Thinning Hair, Wnt Activator Proteins, Wnt Signaling Pathway Posted by