Evidence map›Paper›PMID 32695307›Full record

ReviewTherapeutic advances in endocrinology and metabolism2020

Therapeutic potential of pyruvate therapy for patients with mitochondrial diseases: a systematic review.

Min Li, Shuang Zhou, Chaoyang Chen, Lingyun Ma, Daohuang Luo, Xin Tian, Xiu Dong, Ying Zhou, Yanling Yang, Yimin Cui

Open access · goldAbstract readReview
In one paragraph

Review in Therapeutic advances in endocrinology and metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 25% of its field
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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Therapies for Mitochondrial Disease: Past, Present, and Future.Journal of inherited metabolic disease · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. Metabolomics in aging research: aging markers from organs.Frontiers in cell and developmental biology · 2023
    Review
  9. Article
  10. Article
  11. Article
  12. NADNutrition and metabolic insights · 2021
    Review
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

10 authors at 1 institution in 1 country.

Min LiDepartment of Pharmacy, Peking University First Hospital, Beijing, China.
Shuang ZhouDepartment of Pharmacy, Peking University First Hospital, Beijing, China.
Chaoyang ChenDepartment of Pharmacy, Peking University First Hospital, Beijing, China.
Lingyun MaDepartment of Pharmacy, Peking University First Hospital, Beijing, China.
Daohuang LuoDepartment of Pharmacy, Peking University First Hospital, Beijing, China.
Xin TianDepartment of Pharmacy, Peking University First Hospital, Beijing, China.
Xiu DongDepartment of Pharmacy, Peking University First Hospital, Beijing, China.
Ying ZhouDepartment of Pharmacy, Peking University First Hospital, Beijing, China.
Yanling YangDepartment of Pediatrics, Peking University First Hospital, 8 Xishiku Street, Xicheng District, Beijing, 100034, China.
Yimin CuiDepartment of Pharmacy, Peking University First Hospital, 6 Dahongluochang Street, Xicheng District, Beijing, 100034, China.ORCID https://orcid.org/0000-0002-4186-1005
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMitochondrial disease is a term used to describe a set of heterogeneous genetic diseases caused by impaired structure or function of mitochondria. Pyruvate therapy for mitochondrial disease is promising from a clinical point of view.

methodsAccording to PRISMA guidelines, the following databases were searched to identify studies regarding pyruvate therapy for mitochondrial disease: PubMed, EMBASE, Cochrane Library, and

resultsA total of six studies were included. Considerable differences were noted between studies in terms of study design, patient information, and outcome measures. The collected evidence may indicate an effective potential of pyruvate therapy on the improvement of mitochondrial disease. The majority of the common adverse events of pyruvate therapy were diarrhea and short irritation of the stomach.

conclusionPyruvate therapy with no serious adverse events may be a potential therapeutic candidate for patients with incurable mitochondrial diseases, such as Leigh syndrome. However, recent evidence taken from case series and case reports, and theoretical supports of basic research are not sufficient. The use of global registries to collect patient data and more adaptive trial designs with larger numbers of participants are necessary to clarify the efficacy of pyruvate therapy.

Indexed as

mitochondrial diseasepyruvate therapysystematic review

Identifiers

PMID32695307
PMCPMC7350055
OpenAlexW3041210126

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.