Rheumatoid Arthritis Medication May Help Asthma Patients
Editor's ChoiceAcademic Journal
Main Category: Respiratory / Asthma
Also Included In: Genetics
Article Date: 09 Sep 2011 - 9:00 PDT
'Rheumatoid Arthritis Medication May Help Asthma Patients'
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A drug used today to treat rheumatoid arthritis might be effective in treating asthma symptoms after two genetic variants have been found to increase asthma susceptibility, researchers from the Queensland Institute of Medical Research, Brisbane, Australia and others from around the world reported in The Lancet. The scientists found that cytokines - genes associated with signalling molecules that are involved in how the immune system functions - are involved in the development of asthma.
The authors explained that the causes of asthma have for long been poorly understood, in spite of several attempts to locate the genetic variants. Some recent GWAS (genome-wide associated studies) have only managed to locate some candidate genes which appear to have a slight effect on asthma risk. They have not fully explained the heritability of asthma, which leads doctors and scientists to believe that many genetic variations are involved.
Manuel Ferreira and an international team of experts set out to determine what genetic variations might be responsible for higher asthma risk by carefully examining all current GWAS and expanding on them.
They compared the genomes of thousands of asthma patients with individuals who do not have asthma across several populations and identified two genetic mutations that were strongly linked to asthma risk.
The genetic variants were:
- rs4129267 in the interleukin-6 receptor (IL6R) gene, and
- rs7130588 on chromosome 11q13.5
The drug tocilizumab is an example of a medication that blocks the receptor. It is already approved for rheumatoid arthritis treatment.
A high proportion of atopic (allergic) asthma patients were found to have the rs7130588 variant on chromosome 11q13.5. Interestingly, it was correlated with a nearby variant which has been recently associated with atopic dermatitis risk.
The authors believe that a gene in this region is involved in the development of allergic sensitisation, which raises allergic asthma risk.
The authors wrote:
"At this stage it is unclear which gene underlies the association with 11q13.5. Given that no specific gene in this region has been directly implicated in allergic disease previou. sly, further characterisation of this region of association is likely to discover novel molecular mechanisms involved in the causality of eczema, atopy, and asthma."
So far, no single genetic cause has been located which is responsible for over 1% of asthma heritability, the authors added. Their findings demonstrate that asthma is a complex condition, and most likely several genes of small effect combine and interact with environmental risk factors in driving asthma risk.
The scientists concluded:
"Our results are consistent with the contribution of hundreds or potentially thousands of variants with weak effects on asthma risk, which can be identified through larger GWAS as already shown with other diseases."
Kathleen Barnes, from Johns Hopkins University, Baltimore, USA, in a Comment in the same journal wrote:
"Success in the validation of various candidates (and their pathways) that are already on the asthma shortlist of potential causal genes, and the biological insight to be gained from the novel findings in this report are grounds for optimism in the continuation of the GWAS approach. Combination of GWAS with next-generation technologies will undoubtedly further help to disentangle the molecular underpinnings of complex traits such as asthma."
Written by Christian Nordqvist
Copyright: Medical News Today
Not to be reproduced without permission of Medical News Today
Dr Manuel AR Ferreira, Melanie C Matheson PhD, David L Duffy PhD, Prof Guy B Marks FRACP, Jennie Hui PhD, Prof Peter Le Souëf FRACP , Patrick Danoy PhD, Svetlana Baltic PhD, Dale R Nyholt PhD, Mark Jenkins PhD, Catherine Hayden PhD, Gonneke Willemsen PhD, Wei Ang MSc l, Mikko Kuokkanen PhD, John Beilby PhD, Faang Cheah BSc, Eco JC de Geus PhD, Adaikalavan Ramasamy DPhil, Sailaja Vedantam PhD, Veikko Salomaa PhD, Pamela A Madden PhD, Prof Andrew C Heath DPhil, Prof John L Hopper PhD, Peter M Visscher PhD, Prof Bill Musk FRACP, Prof Stephen R Leeder FRACP, Prof Marjo-Riitta Jarvelin MD, Craig Pennell PhD, Prof Dorret I Boomsma PhD, Prof Joel N Hirschhorn MD, Prof Haydn Walters FRACP, Prof Nicholas G Martin PhD, Alan James FRACP, Graham Jones PhD, Prof Michael J Abramson PhD, Colin F Robertson FRACP, Shyamali C Dharmage PhD, Prof Matthew A Brown FRACP, Grant W Montgomery PhD, Prof Philip J Thompson FRACP
The Lancet, Volume 378, Issue 9795, Pages 1006 - 1014, 10 September 2011. doi:10.1016/S0140-6736(11)60874-X
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