Evidence map›Paper›PMID 37182927›Full record

ArticleSaudi medical journal2023

Clinical and laboratory characteristics of idiopathic inflammatory myositis in Saudi patients: A retrospective study in a single tertiary centre.

Fahidah Alenzi, Jawaher Alotaibi, Manal Alnasser, Fahdah Alokaily

Abstract read
In one paragraph

Article in Saudi medical journal, 2023. 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
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  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

4 authors.

Fahidah AlenziFrom the Department of Clinical Science (Alenzi), College of Medicine, Princess Nourah bint Abdulrahman University; and from the Division of Rheumatology, Department of Medicine (Alotaibi, Alnasser, Alokaily), Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia.
Jawaher AlotaibiFrom the Department of Clinical Science (Alenzi), College of Medicine, Princess Nourah bint Abdulrahman University; and from the Division of Rheumatology, Department of Medicine (Alotaibi, Alnasser, Alokaily), Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia.
Manal AlnasserFrom the Department of Clinical Science (Alenzi), College of Medicine, Princess Nourah bint Abdulrahman University; and from the Division of Rheumatology, Department of Medicine (Alotaibi, Alnasser, Alokaily), Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia.
Fahdah AlokailyFrom the Department of Clinical Science (Alenzi), College of Medicine, Princess Nourah bint Abdulrahman University; and from the Division of Rheumatology, Department of Medicine (Alotaibi, Alnasser, Alokaily), Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIdiopathic inflammatory myositis (IIM) in Saudi patients has been poorly studied owing to the lack of available data. This study aimed to identify the clinical and laboratory features of patients at a single tertiary care center.

methodsThis retrospective study reviewed the medical records of Prince Sultan Military Medical City, Riyadh, Saudi Arabia to collect clinical and laboratory data between December 2022 and February 2017 as follows: age at disease onset, gender, follow-up duration and disease duration; clinical symptoms; laboratory result; presence and type of myositis-specific autoantibody or myositis-associated autoantibody; and type of immunosuppression, presence of malignancy, disease course, and outcome.

resultsThere were 26 patients with a mean age of 36.16±13.48, and 84.6% were women. The most prevalent form of IIM was dermatomyositis (n=16, 61.5%), and the most affected organ was the skin. weakness was observed in 25 patients (96.2%), and dysphagia was the most common alarm sign (n=10, 38.5%). During follow-up, the creatine kinase level was elevated at the beginning of the disease and then decreased following treatment, with a mean of 277.73 IU/L. Of the total patients, 17 (68%) were positive for anti-nuclear antibody and 5 (19.2%) were positive for anti-Jo-1.

conclusionIn our patients, dermatomyositis was the most common form of myositis, and skin manifestations were the most prevalent clinical characteristics. None of the patients developed a malignancy or died.

Indexed as

DermatomyositisMyositisNeoplasmsAutoantibodiesFemaleHumansMaleRetrospective StudiesSaudi ArabiaAutoantibodiesdermatomyositisidiopathic inflammatory myositismuscle weaknessSaudi Arabia

Identifiers

PMID37182927
PMCPMC10187745

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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.