Priority 16 from the Mitochondrial Disease PSP
UNCERTAINTY: What can prevent the start of mitochondrial disease in people with a genetic mutation? (JLA PSP Priority 16) | |
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Overall ranking | 16 |
JLA question ID | 0095/16 |
Explanatory note | Not available |
Evidence |
https://pubmed.ncbi.nlm.nih.gov/31091381%20https://pubmed.ncbi.nlm.nih.gov/30319102%20 |
Health Research Classification System category | Metabolic and Endocrine |
Extra information provided by this PSP | |
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Original uncertainty examples | how to prevent clinical disease onset ~ New treatments to prevent clinical disease from developing in those at risk ~ Does early diagnosis and treatment with new drugs prevent blindness in patients who are carriers of mitochondrial mutations predisposing to LHON? ~ How can we prevent first eye involvement? ~ What to avoid [TRIGGERS FOR LHON] ~ Can triggers be avoided? Is it possible to avoid triggering the condition? ~ treatment options, information on disease progression, screening for potential complications to treat them early, options to prevent disease ~ To what extent do non genetic components influence disease phenotype and to what extent can these be influenced. ~ Prevention/ control of these factors ?! [TRIGGERS] ~ Are there known risk factors that could have prevented this disease? |
Submitted by |
6 x Healthcare Professional, 3 x Carer, 1 x Patient |
PSP information | |
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PSP unique ID | 0095 |
PSP name | Mitochondrial Disease |
Total number of uncertainties identified by this PSP. | 42 (To see a full list of all uncertainties identified, please see the detailed spreadsheet held on the JLA website) |
Date of priority setting workshop | 19 January 2020 |