ECTS/Alliance for Better Bone Health (Procter & Gamble Pharmaceuticals and sanofi-aventis) Iain T Boyle Award

We are pleased to announce that the deadline for nominations for the Iain Boyle Award has been extended to 5 December 2008. Please submit your nomination here.

2008 Award Announcement

Professor Iain Thomson Boyle (1935-2001) contributed greatly to the field of mineral metabolism and his work on osteoporosis was known and acclaimed nationally and internationally. The 2008 award will be announced during the 35th European Symposium on Calcified Tissues in Barcelona 24-28 May 2008. The award is for €5000 (Euros)

Eligibility

This award is open to young scientists who have made significant progress and contribution to the field of bone and calcified tissue. The nominee should be within 10 years of completing their PhD (or equivalent).

Review Procedure

All applications are reviewed by an independent panel of reviewers. The final decision is based on the marks and comments from the reviewers and any conflicts of interest are identified and dealt with appropriately.

2008 Award

The 2008 ECTS/Alliance for Better Bone Health Iain T Boyle Award was presented on Tuesday 27 May to Dr Rutger van Bezooijen from the Leiden University Medical Center, The Netherlands. Dr Bezooijen’s current interest is focused on characterization of the mechanism by which sclerostin affects Wnt signaling, the regulation of sclerostin expression, and detailed clinical analysis of patients with sclerosteosis and van Buchem disease.


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2008 award winner Rutger van Bezooijen with The Alliance for Better Bone Health representatives Oscar Fillat and David Cahall and ECTS President Richard Eastell

2007 Award

Dr Uwe Kornak was selected as the fifth recipient of the ECTS/Alliance for Better Bone Health Iain T Boyle award, which was presented during the 34th European Symposium on Calcified Tissues in Copenhagen on 8 May 2007. Uwe Kornak is based at the Institute for Medical Genetics in Berlin, Germany and his main interests are the regulation of bone density and NFI and bone. His main focus in the past has been the pathogenesis of recessive and dominant forms of osteopetrosis, which turned out to be caused by defects in intracellular acidification mechanisms. He has subsequently become involved with developmental aspects of skeletogenesis and the role of different transcription factors like Hoxd13, Runx2 and Mef2c. Recently, the scope of his interests was further broadened by investigations on Golgi function in bone homestasis.

 

2006 Award

Dr Florent Elefteriou was selected as the fourth recipient of the Alliance for Better Bone Health Iain T Boyle award.

Dr Elefteriou was trained in biochemistry and genetics in Claude-Bernard University (France) and then Baylor College of Medicine (USA) and is leading since 2005 his own research group at UT-Health Science Center of San Antonio. His major scientific contribution to the bone field has been to uncover the role of the central and peripheral nervous systems in the regulation of bone remodeling.

His seminal work has demonstrated that hypothalamic neurons responsive to the adipocyte-derived hormone leptin inhibits bone formation and favor bone resorption via the sympathetic nervous system and b2-adrenergic receptors expressed by osteoblasts. He has also identified using number of mutant mouse models the neuropeptide CART and the melanocortin 4 receptor as additional and possible central molecules involved in bone mass homeostasis.

His current research focuses on b2-adrenergic signaling in osteoblats and on the characterization of the molecular mechanisms causing the skeletal defects observed in Neurofibromatosis.

2005 Award

Dr Tjeerd van Staa was selected as the third recipient of the Alliance for Better Bone Health (Procter & Gamble Pharmaceuticals and Sanofi-Aventis) award. Dr van Staa has made major contributions to the epidemiology of osteoporosis, with particular regard to glucocorticoid-induced bone loss.  His seminal work has demonstrated that fracture risk in glucocorticoid treated patients rises steeply soon after commencement of therapy; attenuates rapidly after cessation of therapy; and occurs at prednisolone doses less than those conventionally associated with osteoporosis.  His scholarly contributions have had a major input upon clinical practice and have been highly cited in the peer reviewed literature.  He continues to hold academic positions at the MRC Epidemiology Resource Centre, University of Southampton and Institute for Pharmaceutical Sciences, Utrecht University, the Netherlands.

2004 Award

Wim Van Hul was selected as the second recipient of the prestigious Alliance for Better Bone Health Iain T. Boyle award.  He is a researcher trained in molecular biology and genetics who started, after his PhD studies on the genetics of Alzheimer's disease, his own research team at the Department of Medical Genetics at the University and University Hospital in Antwerp, Belgium. In the last decennium, his team has been very successful in identifying and characterizing genes underlying, mainly monogenic, genetic conditions associated with an abnormal bone homeostasis.  These include the SOST gene underlying Van Buchem disease and sclerosteosis, the role of TGFbeta-1 in Camurati-Engelmann disease, the chloride channel ClCN7 in autosomal dominant osteopetrosis, LRP5 in different sclerosing bone dysplasias as well as the involvement of Msx2 and Alx4 in ossification defects of the skull. He is currently coauthor of about 80 publications, many of them in journals of high impact.

2003 Award

Michael Rogers is an outstanding young scientist and is a worthy recipient of this prestigious award. His major scientific achievement has been to elucidate the molecular mechanisms of action of bisphosphonate drugs. He and his group are at the forefront of this research and have clearly shown that bisphosphonates act on osteoclasts by two distinct mechanisms. Simple bisphosphonates become incorporated into toxic ATP analogues that induce osteoclast apoptosis, whereas the more potent nitrogen-containing bisphosphonates prevent prenylation of small GTPase signalling proteins by inhibiting the enzyme FPP synthase. He started this research on bisphosphonates during his PhD studies in 1989 and over the following decade has produced a very impressive number of publications.

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