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SMCI honored to partner on three NIH-funded centers

Emily Taylor

Senior Member
Messages
149
Location
Los Angeles, CA
September 27, 2017

Breaking News: NIH Announces Results of ME/CFS Program Awards
The National Institutes of Health (NIH) announced today the outcome of its ME/CFS (myalgic encephalomyelitis/chronic fatigue syndrome) competitive consortium grants, marking an unprecedented and tangible commitment from the federal agency to the disease. The NIH announced four recipient teams; one Data Management Coordination Center (DMCC) and three Collaborative Research Centers (CRCs).

The team selected to lead the development of the Data Management Coordination Center (DMCC) will serve as the keystone to centralize, share and standardize the data of the ME/CFS Collaborative Research Centers.
  • Dr. Rick Williams (RTI International) in partnership with Dr. Peter Rowe (Johns Hopkins School of Medicine (JHSM)) and Dr. Zaher Nahle (SMCI).
The three teams selected to lead the development of the Collaborative Research Centers (CRCs) represent an incredible breadth and depth of expertise from prestigious institutions.
  • Dr. Ian Lipkin (Columbia University) and team, with SMCI as collaborator
  • Dr. Maureen Hanson (Cornell University) and team, with SMCI as a collaborator
  • Dr. Derya Unutmaz (the Jackson Laboratory for Genomic Medicine (JAX) ) and team.

Since the funding announcement was released in January, the ME/CFS community has waited anxiously to hear the results for this new era of ME/CFS research. The response to the NIH grant solicitations was strong, attracting high caliber applicants. These submissions included expertise in immunity, inflammation, neuroendocrine biology, bioenergetics, epidemiology, biostatistics, clinical care, and clinical management, some of whom were applying their talent for the first time in the ME/CFS field.

The Solve ME/CFS Initiative (SMCI) was honored participate in seven proposals during the application process. It was a privilege to work with diverse applicants, all of whom embody of our organization’s mission to make ME/CFS understood, diagnosable, and treatable. We serve as a credible scientific partner and a trusted resource for everyone who is creating value in our disease space. We will continue to maintain and pursue those collaborations with proposals that were not funded, in addition to our role with the NIH-funded centers.

As partners of the DMCC proposal led by Dr. Rick Williams (RTI), with Dr. Zaher Nahle (SMCI) and Dr. Peter Rowe (JHSM, SMCI RAC) as co-investigators, our organization is committed to advancing the field through big data analysis and electronic health record systems.

"We are thrilled to be part of that effort in what is a landmark turning point development for our disease,” said Dr. Nahle, Chief Scientific officer and VP for Research, the creator of these strategic partnerships
The forthcoming SMCI patient registry is a key component of the DMCC effort. As collaborators with the new CRCs lead investigators, Dr. Ian Lipkin (Columbia CRC), Dr. Maureen Hanson (Cornell CRC and SMCI RAC) and longtime SMCI colleague Dr. Derya Unutmaz (JAX CRC), we continue to create value and facilitate the work of all investigators, through the CRCs, DMCC, and beyond.
Carol Head, SMCI President, noted “The NIH consortium grants are a much anticipated commitment of federal funds to solve this devastating disease. We hope and trust these consortia, along with the NIH intramural study, represent the dawning of a desperately needed, rapid expansion of the Federal commitment to ME/CFS.”
The awarded proposals emerged from a competitive process in response to two funding opportunity announcements (FOAs) in January 2017. These grants are a mechanism by which federal agencies announce their intent to fund discretionary grants or cooperative agreements.
  • A U54-designated FOA invited applications for ME/CFS Collaborative Research Centers (CRCs); the goal of the ME/CFS CRCs is to create a network of specialized centers that will both advance independent initiatives and work collaboratively to establish the cause(s) of ME/CFS and work towards the development of improved treatments.
  • A U24-designated FOA was created to establish a Data Management and Coordinating Center (DMCC). The goal of the ME/CFS DMCC is to streamline and improve data management and sharing to support the efforts of the ME/CFS CRCs. The network of CRCs, linked with the DMCC, will create a robust infrastructure and bring a comprehensive and integrated approach to ME/CFS research.

Once again, congratulations to the four newly funded organizations and we are honored to be included in three of these projects, including playing a central role at the DMCC alongside colleagues at RTI international. We appreciate this tangible commitment by the NIH, which actualizes the intent announced by NIH Director Dr. Francis Collins in 2015, efforts undertaken by Dr. Koroshetz, the director of the National Institute of Neurological Disorders and Stroke (NINDS), as well as Dr. Vicky Whittemore and Dr. Avindra Nath, lead investigator of the intramural study at the NIH.

Please stay tuned for updates and announcements as the four new programs develop. You can join join the Solve ME/CFS Initiative's mailing list here for weekly updates on items relating to the organization and the ME/CFS community.
 

Barry53

Senior Member
Messages
2,391
Location
UK
The very fact NIH is investing serious money into serious biomedical research into ME, really should make others sit up and take heed. As well as the research investment itself, I would think it has significant political and advocacy implications world wide. Hopefully David Tuller will have picked up on this, because it gives ever more credibility to the arguments he puts forward on our behalf.