Evidence map›Paper›PMID 27896103›Full record

ArticleMolecular genetics and metabolism reports2014

Plasma mutant α-galactosidase A protein and globotriaosylsphingosine level in Fabry disease.

Takahiro Tsukimura, Sachie Nakano, Tadayasu Togawa, Toshie Tanaka, Seiji Saito, Kazuki Ohno, Futoshi Shibasaki, Hitoshi Sakuraba

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics and metabolism reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Pathogenic mechanisms in Fabry disease.Frontiers in medicine · 2026
    Review
  3. Article
  4. Article
  5. Evaluation ofMolecular genetics and metabolism reports · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

8 authors at 4 institutions in 1 country.

Takahiro TsukimuraDepartment of Functional Bioanalysis, Meiji Pharmaceutical University, Tokyo, Japan.
Sachie NakanoDepartment of Molecular Medical Research, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan; Synthera Technologies, Co., Ltd., Tokyo, Japan.
Tadayasu TogawaDepartment of Functional Bioanalysis, Meiji Pharmaceutical University, Tokyo, Japan.
Toshie TanakaDepartment of Clinical Genetics, Meiji Pharmaceutical University, Tokyo, Japan.
Seiji SaitoDepartment of Medical Management and Informatics, Hokkaido Information University, Hokkaido, Japan.
Kazuki OhnoNPO for the Promotion of Research on Intellectual Property Tokyo, Tokyo, Japan.
Futoshi ShibasakiDepartment of Molecular Medical Research, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
Hitoshi SakurabaDepartment of Clinical Genetics, Meiji Pharmaceutical University, Tokyo, Japan.
Meiji Pharmaceutical University · JPTokyo Metropolitan Institute of Medical Science · JPHokkaido Information University · JPJapan Patent Office · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fabry disease is an X-linked genetic disorder characterized by deficient activity of α-galactosidase A (GLA) and accumulation of glycolipids, and various GLA gene mutations lead to a wide range of clinical phenotypes from the classic form to the later-onset one. To investigate the biochemical heterogeneity and elucidate the basis of the disease using available clinical samples, we measured GLA activity, GLA protein and accumulated globotriaosylsphingosine (Lyso-Gb3), a biomarker of this disease, in plasma samples from Fabry patients. The analysis revealed that both the enzyme activity and the protein level were apparently decreased, and the enzyme activity was well correlated with the protein level in many Fabry patients. In these cases, a defect of biosynthesis or excessive degradation of mutant GLAs should be involved in the pathogenesis, and the residual protein level would determine the accumulation of Lyso-Gb3 and the severity of the disease. However, there are some exceptional cases, i.e., ones harboring p.C142Y, p.R112H and p.M296I, who exhibit a considerable amount of GLA protein. Especially, a subset of Fabry patients with p.R112H or p.M296I has been attracted interest because the patients exhibit almost normal plasma Lyso-Gb3 concentration. Structural analysis revealed that C142Y causes a structural change at the entrance of the active site. It will lead to a complete enzyme activity deficiency, resulting in a high level of plasma Lyso-Gb3 and the classic Fabry disease. On the other hand, it is thought that R112H causes a relatively large structural change on the molecular surface, and M296I a small one in a restricted region from the core to the surface, both the structural changes being far from the active site. These changes will cause not only partial degradation but also degeneration of the mutant GLA proteins, and the degenerated enzymes exhibiting small and residual activity remain and probably facilitate degradation of Lyso-Gb3 in plasma, leading to the later-onset phenotype. The results of this comprehensive analysis will be useful for elucidation of the basis of Fabry disease.

Indexed as

Fabry diseaseGlobotriaosylsphingosineStructural modelingα-Galactosidase A

Identifiers

PMID27896103
PMCPMC5121323
OpenAlexW1972506035

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.