Evidence map›Paper›PMID 35479934›Full record

ArticleFrontiers in medicine2022

Health-Related Quality of Life Evaluation Using the Short Form-36 in Patients With Human T-Lymphotropic Virus Type 1-Associated Myelopathy.

Miyuna Kimura, Junji Yamauchi, Tomoo Sato, Naoko Yagishita, Natsumi Araya, Satoko Aratani, Kenichiro Tanabe, Erika Horibe, Toshiki Watanabe, Ariella Coler-Reilly and 10 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 97% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. 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

20 authors at 3 institutions in 2 countries.

Miyuna KimuraDepartment of Anesthesiology, St. Marianna University School of Medicine, Kawasaki, Japan.
Junji YamauchiDepartment of Rare Diseases Research, Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Japan.
Tomoo SatoDepartment of Rare Diseases Research, Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Japan.
Naoko YagishitaDepartment of Rare Diseases Research, Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Japan.
Natsumi ArayaDepartment of Rare Diseases Research, Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Japan.
Satoko ArataniDepartment of Rare Diseases Research, Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Japan.
Kenichiro TanabeDepartment of Frontier Medicine, Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Japan.
Erika HoribeDepartment of Practical Management of Medical Information, St. Marianna University Graduate School of Medicine, Kawasaki, Japan.
Toshiki WatanabeDepartment of Practical Management of Medical Information, St. Marianna University Graduate School of Medicine, Kawasaki, Japan.
Ariella Coler-ReillyDepartment of Rare Diseases Research, Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Japan.
Misako NagasakaDepartment of Rare Diseases Research, Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Japan.
Yukari AkasuDivision of Neurology, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.
Kei KaburagiDivision of Neurology, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.
Takayuki KikuchiDivision of Neurology, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.
Soichiro ShibataDivision of Neurology, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.
Hirofumi MatsumotoDivision of Neurology, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.
Akihito KosekiDivision of Neurology, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.
Soichiro InoueDepartment of Anesthesiology, St. Marianna University School of Medicine, Kawasaki, Japan.
Ayako TakataDepartment of Preventive Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.
Yoshihisa YamanoDepartment of Rare Diseases Research, Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Japan.
St. Marianna University School of Medicine · JPShizuoka University of Welfare · JPUniversity of California, Irvine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Human T-lymphotropic virus type 1 (HTLV-1)-associated myelopathy (HAM) is a neuroinflammatory disease, causing various neurological symptoms, including motor, sensory, and bladder and bowel dysfunctions. This study was designed to reveal the impact of HAM and related symptoms on health-related quality of life (HRQoL). Methods: We analyzed the Short Form-36 (SF-36) and clinical data of 538 patients with HAM registered in the HAM-net, a nationwide patient registry for HAM in Japan. HRQoL was evaluated using the SF-6D (a health state utility value calculated from the SF-36) and eight SF-36 subscales. A general liner model was used to estimate the impact of major HAM-related symptoms, including gait dysfunction, sensory disturbance in the legs (pain and numbness), urinary dysfunction, and constipation, on the SF-6D and SF-36 subscale scores. Results: The mean age and disease duration were 62.0 and 16.5 years, respectively. Of the patients, 73.2% needed walking aid; 42.7 and 67.1% had leg pain and numbness, respectively; 92.1% had urinary dysfunction; and 77.9% had constipation. The mean SF-6D score was 0.565, which was significantly lower than the national average (0.674 in the 60-69 years age group; Conclusion: HRQoL of patients with HAM was worse than that of the general population and was associated with all major symptoms. Thus, patients should be comprehensively managed to achieve better HRQoL.

Indexed as

HTLV-1HTLV-1-associated myelopathyquality of lifeSF-36SF-6D

Identifiers

PMID35479934
PMCPMC9036434
OpenAlexW4223634045

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.