This news may lead to a hope for better
hair loss treatment we are looking for. A
new gene involved in hair growth was identified by the investigators
from Columbia, Rockefeller and Stanford Universities in the April 15 issue of Nature.
This discovery may affect future research and treatments for men pattern
baldness and other forms of hair loss.
The researchers found that the gene,
called APCDD1, which causes a progressive form of hair loss beginning in
childhood (known as hereditary hypotrichosis simplex). The disease is caused by
a phenomenon called hair follicle miniaturization -- the same key feature of
male pattern baldness. When hair follicles go through this miniaturization
process, they shrink or narrow, causing the thick hair on the head to be
replaced by thin, fine hair, known as "peach fuzz."
"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,"
said Angela M. Christiano, Ph.D., professor of dermatology and genetics &
development at Columbia University Medical Center, and lead author of the
study. "It is important to note that while these two conditions share the
same physiologic process, the gene we discovered for hereditary hypotrichosis
does not explain the complex process of male pattern baldness."
The team made their discovery by
analyzing genetic data from a few families from Pakistan and Italy with
hereditary hypotrichosis simplex. They found a common mutation in the APCDD1
gene, which is located in a specific region on chromosome 18 that has been
shown in previous studies to be implicated in other forms of hair loss, including
androgenetic alopecia and alopecia areata, hinting at a broader role in hair
follicle biology.
Importantly, the researchers found
that APCDD1 inhibits a signaling pathway that has long been shown to control hair
growth in mouse models, but has not been extensively linked to human hair
growth. Laboratory researchers have targeted this pathway, known as the Wnt
signaling pathway, to turn on or off hair growth in mice, but, until now, the
pathway did not appear to be involved in human hair loss. This finding
is significant because it provides evidence that hair growth patterns in humans
and in mice are more similar than previously believed.
"We have at last made a
connection between Wnt signaling and human hair disease that is highly
significant," said Dr. Christiano. "We have years of beautiful data
in our field about hair growth in mice, but this is the first inroad into
showing that the same pathway is critical in human hair growth. This is the
first mutation in a Wnt inhibitor that deregulates the pathway in a human hair
disease."
"Furthermore, these findings
suggest that manipulating the Wnt pathway may have an effect on hair follicle
growth -- for the first time, in humans," said Dr. Christiano. "And
unlike commonly available treatments for hair loss that involve blocking
hormonal pathways, treatments involving the Wnt pathway would be non-hormonal,
which may enable many more people suffering from hair loss to receive such
therapies."
Dr. Christiano and her team are now
working to understand the complex genetic causes of other forms of hair loss
including alopecia areata, with the hope of eventually developing new,
effective treatments for these conditions.
However, it needs more supportive researches and long trails for scientific data for the effect on human. In this view, many doctors still prefer to recommend integrative medicines for hair loss and baldness. This includes drug treatment, surgical and cosmetic treatments, complementary and alternative treatments, all we try to digest and make it as easy as possible to understand cause of hair loss, receding hair lines and baldness in order to get the best result.
Referenece:
Columbia
University Medical Center (2010, April 14). New gene in hair loss identified. ScienceDaily. Retrieved
September 22, 2011
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