Evidence map›Paper›PMID 30867548›Full record

ArticleJournal of human genetics2019

Investigating the role of genetic counseling in neuromuscular disease considering life events.

Yuka Shibata, Ichiro Yabe, Masaaki Matsushima, Naoki Hashimoto, Takahiro Yamada, Hidenao Sasaki

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of human genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Genetic Testing for Neuromuscular Diseases.Practical neurology (Fort Washington, Pa.) · 2024
    Article
  2. 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

6 authors at 4 institutions in 1 country.

Yuka ShibataDivision of Clinical Genetics, Hokkaido University Hospital, Sapporo, Japan.ORCID http://orcid.org/0000-0003-3752-5946
Ichiro YabeDivision of Clinical Genetics, Hokkaido University Hospital, Sapporo, Japan. yabe@med.hokudai.ac.jp.ORCID http://orcid.org/0000-0002-1734-7997
Masaaki MatsushimaDivision of Clinical Genetics, Hokkaido University Hospital, Sapporo, Japan.ORCID http://orcid.org/0000-0001-6585-3686
Naoki HashimotoDepartment of Psychiatry, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Takahiro YamadaClinical Genetics Unit, Kyoto University Hospital, Kyoto, Japan.ORCID http://orcid.org/0000-0002-5370-7873
Hidenao SasakiDivision of Clinical Genetics, Hokkaido University Hospital, Sapporo, Japan.
Hokkaido University · JPHokkaido University Hospital · JPKyoto University Hospital · JPSapporo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic diagnoses are becoming a routine in the medical practice of neuromuscular diseases. Many diagnoses, however, can have an influence on relatives and family members and thus must be handled carefully by genetic counseling (GC). Here, we aimed to assess the purpose of undergoing GC to verify the utility of collaborations between clinical and genetic divisions. We investigated consecutive GC cases of neuromuscular disease and examined the role of GC. Our study included 102 cases who underwent GC in our hospital from July 2005 to March 2018: 86.3% were women and 45.1% were in their 30's. Disease explanation was the most common reason for attending GC (29.4%), followed by prenatal diagnosis (25.5%), pre-symptomatic diagnosis (17.6%), and carrier diagnosis (14.7%). Clients typically visited the hospital for GC when some kind of life event occurred, such as marriage, had a desire to bear a child, or a change in the condition of the proband. Clinicians should be conscious of such life events from the perspective of both the client and their relatives, and guide the GC at an appropriate time. Overall, the degree of recognition of genetic risk by clients differed; thus, it is important for GC to determine the status of each unique situation and respond individually.

Indexed as

FamilyGenetic CounselingAdultFemaleGenetic Carrier ScreeningGenetic TestingHumansMaleMiddle AgedNeuromuscular DiseasesPedigreeRisk FactorsYoung Adult

Identifiers

PMID30867548
OpenAlexW2921963768

What OpenQuestion holds

Textmetadata
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.