Breakthrough Discovery: Misbehaving Mitochondria Linked to Juvenile Dermatomyositis

Research Update: misbehaving Mitochondria Linked to Juvenile Dermatomyositis. Dr. Christian Lood

The generous support of our community has been instrumental in funding groundbreaking research this year, led by Dr. Christian Lood at the University of Washington and Cure JM’s Center of Excellence at Seattle Children’s Hospital.

With a keen focus on understanding the role of mitochondria, the cell’s energy powerhouses, in juvenile dermatomyositis (JDM), Dr. Lood’s team has made a significant discovery. They have identified calcified mitochondria in the muscle tissue of JDM patients with calcinosis – a finding that sheds new light on understanding JDM.

This groundbreaking research opens the door to potential new treatments for JDM

“By targeting misbehaving mitochondria and inflammation, we aim to develop more effective therapies,” says Dr. Lood. “Additionally, we are working to identify unique mitochondrial biomarkers to tailor individual treatment plans for individual patients.”

In the coming year, Dr. Lood will continue to explore:

  • New treatment targets based on mitochondrial function
  • Developing individual treatment plans using mitochondrial biomarkers
  • The long-term impact of misbehaving mitochondria on JDM and how we might prevent disease progression – essentially stopping JDM in its tracks
  • Collaborations with other research institutions

We are excited about the potential of this new research to improve the lives of children. We will continue to keep you informed on this evolving project and others as they develop.

To learn more about all of the research projects addressing our mission, visit www.curejm.org/impact.

Walking Strong – Empowered by Unity

Like other teens new to the JM journey, Catie Beth Caldwell and Madi Cook were two individuals who felt alone at the beginning of their journeys. Catie Beth was diagnosed just before the Covid-19 pandemic took hold of the world as we knew it. With this came feelings of isolation and loneliness. These emotions were commonplace for many teens but were only compounded by teens new to a rare disease diagnosis. These first years of the “new normal” were difficult to navigate.

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