Evidence map›Paper›PMID 30301846›Full record

ReviewBiochemical Society transactions2018

Towards a therapy for mitochondrial disease: an update.

Caterina Garone, Carlo Viscomi

Abstract readReview
In one paragraph

Review in Biochemical Society transactions, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Review
  6. Hypoxia as a medicine.Science translational medicine · 2025
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Recent advances in mitochondrial diseases: From molecular insights to therapeutic perspectives.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2022
    Review
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Caterina GaroneMRC-Mitochondrial Biology Unit, Cambridge CB2 0XY, U.K. cg562@mrc-mbu.cam.ac.uk cfv23@mrc-mbu.cam.ac.uk.
Carlo ViscomiMRC-Mitochondrial Biology Unit, Cambridge CB2 0XY, U.K. cg562@mrc-mbu.cam.ac.uk cfv23@mrc-mbu.cam.ac.uk.

Funding

Medical Research Council MC_EX_MR/P007031/1Medical Research Council MC_EX_MR/P007031/1]Medical Research Council MC_UU_00015/5Medical Research Council MC_UU_00015/8
6 · The paper itself

Abstract

Preclinical work aimed at developing new therapies for mitochondrial diseases has recently given new hopes and opened unexpected perspectives for the patients affected by these pathologies. In contrast, only minor progresses have been achieved so far in the translation into the clinics. Many challenges are still ahead, including the need for a better characterization of the pharmacological effects of the different approaches and the design of appropriate clinical trials with robust outcome measures for this extremely heterogeneous, rare, and complex group of disorders. In this review, we will discuss the most important achievements and the major challenges in this very dynamic research field.

Indexed as

AnimalsAntioxidantsClinical Trials as TopicDiet, KetogenicGenetic TherapyHumansHypoxiaMechanistic Target of Rapamycin Complex 1MitochondriaMitochondrial DiseasesMutationPhenotypeReactive Oxygen SpeciesSirolimusAntioxidantsMechanistic Target of Rapamycin Complex 1Reactive Oxygen SpeciesSirolimusbypass therapygene therapymitochondrial biogenesismitochondrial dysfunctionrapamycin

Identifiers

PMID30301846
PMCPMC6195631

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.