Evidence map›Paper›PMID 25343126›Full record

ArticleIntractable & rare diseases research2014

Radiographic characteristics of the hand and cervical spine in fibrodysplasia ossificans progressiva.

Kenichi Mishima, Hiroshi Kitoh, Nobuhiko Haga, Yasuharu Nakashima, Junji Kamizono, Takenobu Katagiri, Takafumi Susami, Masaki Matsushita, Naoki Ishiguro

Open access · bronzeAbstract read
In one paragraph

Article in Intractable & rare diseases research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. BMP signaling and skeletal development in fibrodysplasia ossificans progressiva (FOP).Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    Review
  5. Review
  6. Article
  7. Article
  8. 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

9 authors at 1 institution in 1 country.

Kenichi MishimaDepartment of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan;
Hiroshi KitohDepartment of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan; ; The Research Committee on Fibrodysplasia Ossificans Progressiva, Tokyo, Japan.
Nobuhiko HagaThe Research Committee on Fibrodysplasia Ossificans Progressiva, Tokyo, Japan.
Yasuharu NakashimaThe Research Committee on Fibrodysplasia Ossificans Progressiva, Tokyo, Japan.
Junji KamizonoThe Research Committee on Fibrodysplasia Ossificans Progressiva, Tokyo, Japan.
Takenobu KatagiriThe Research Committee on Fibrodysplasia Ossificans Progressiva, Tokyo, Japan.
Takafumi SusamiThe Research Committee on Fibrodysplasia Ossificans Progressiva, Tokyo, Japan.
Masaki MatsushitaDepartment of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan;
Naoki IshiguroDepartment of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan;
Nagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibrodysplasia ossificans progressiva (FOP) is a disabling heritable disorder of connective tissue characterized by progressive heterotopic ossification in various extraskeletal sites. Early correct diagnosis of FOP is important to prevent additional iatrogenic harm or trauma. Congenital malformation of the great toes is a well-known diagnostic clue, but some patients show normal-appearing great toes. The thumb shortening and cervical spine abnormalities are other skeletal features often observed in FOP. This study aimed to address the quantitative assessment of these features in a cohort of patients with FOP, which potentially helps early diagnosis of FOP. Radiographs of the hand and cervical spine were retrospectively analyzed from a total of 18 FOP patients (9 males and 9 females) with an average age of 13.9 years (range 0.7-39.3 years). The elevated ratio of the second metacarpal bone to the distal phalanx of the thumb (> +1SD) was a consistent finding irrespective of the patient's age and gender. Infant FOP patients, in addition, exhibited an extremely high ratio of the second metacarpal bone to the first metacarpal bone (> +3SD). The height/depth ratio of the C5 vertebra increased in patients over 4 years of age (> +2SD). Additionally, the ratio of (height+depth) of the C5 spinous process to the C5 vertebral depth was markedly elevated in young patients (> +2SD). We quantitatively demonstrated the hand and cervical spine characteristics of FOP. These findings, which can be seen from early infancy, could be useful for early diagnosis of FOP even in patients without great toe abnormalities.

Indexed as

early diagnosisFibrodysplasia ossificans progressivaradiographic characteristics

Identifiers

PMID25343126
PMCPMC4204539
OpenAlexW2059701448

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.