Evidence map›Paper›PMID 33704661›Full record

ArticleMetabolic brain disease2021

Patients with cerebrotendinous xanthomatosis diagnosed with diverse multisystem involvement.

Pelin Teke Kısa, Gonca Kilic Yildirim, Burcu Ozturk Hismi, Sevil Dorum, Ozge Yilmaz Kusbeci, Ali Topak, Figen Baydan, Fatma Nazlı Durmaz Celik, Orhan Gorukmez, Zumrut Arslan Gulten and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Metabolic brain disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
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

14 authors at 6 institutions in 1 country.

Pelin Teke KısaDepartment of Pediatrics, Division of Pediatric Metabolism and Nutrition, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey.ORCID https://orcid.org/0000-0001-6481-3172
Gonca Kilic YildirimDepartment of Pediatrics, Division of Pediatric Metabolism and Nutrition, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.ORCID https://orcid.org/0000-0001-6769-667X
Burcu Ozturk HismiDepartment of Pediatrics, Division of Pediatric Metabolism and Nutrition, Marmara University Faculty of Medicine, Istanbul, Turkey.ORCID https://orcid.org/0000-0001-7146-0248
Sevil DorumBursa Yuksek Ihtisas Training and Research Hospital, Pediatric Metabolic Diseases Clinic, Bursa University of Health Sciences, Bursa, Turkey.ORCID https://orcid.org/0000-0001-6947-2573
Ozge Yilmaz KusbeciDepartment of Neurology, Izmir Bozyaka Training and Research Hospital, Izmir, Turkey.ORCID https://orcid.org/0000-0002-4048-210X
Ali TopakBursa Yuksek Ihtisas Training and Research Hospital, Medical Genetics Clinic, Bursa University of Health Sciences, Bursa, Turkey.ORCID https://orcid.org/0000-0002-6290-1141
Figen BaydanTepecik Training and Research Hospital, Department of Child Health and Diseases, Division of Pediatric Neurology, Izmir University of Health Sciences, Izmir, Turkey.ORCID https://orcid.org/0000-0001-6853-6555
Fatma Nazlı Durmaz CelikDepartment of Neurology, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.ORCID https://orcid.org/0000-0002-2943-2240
Orhan GorukmezBursa Yuksek Ihtisas Training and Research Hospital, Medical Genetics Clinic, Bursa University of Health Sciences, Bursa, Turkey.ORCID https://orcid.org/0000-0002-9241-0896
Zumrut Arslan GultenDepartment of Pediatrics, Division of Pediatric Metabolism and Nutrition, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey.ORCID https://orcid.org/0000-0003-4970-1759
Arzu EkiciBursa Yuksek Ihtisas Training and Research Hospital, Pediatric Neurology Clinic, Bursa University of Health Sciences, Bursa, Turkey.ORCID https://orcid.org/0000-0002-0813-7189
Serhat OzkanDepartment of Neurology, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.ORCID https://orcid.org/0000-0002-5874-5270
Aylin YamanFaculty of Medicine, Department of Ophthalmology, Dokuz Eylul University, Izmir, Turkey.ORCID https://orcid.org/0000-0002-0391-5420
Nur ArslanDepartment of Pediatrics, Division of Pediatric Metabolism and Nutrition, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey. nur.arslan@deu.edu.tr.ORCID https://orcid.org/0000-0003-3151-3741
Sağlık Bilimleri Üniversitesi · TREskişehir Osmangazi University · TRIzmir University · TRDokuz Eylül University · TRIzmir Bozyaka Eğitim ve Araştırma Hastanesi · TRMarmara University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebrotendinous xanthomatosis (CTX) is a lipid storage disease caused by deficiency of sterol 27-hydroxylase enzyme encoded by CYP27A1 gene. This multicenter, cross-sectional descriptive study aimed to document clinical characteristics of CTX patients of different ages, clinical presentations of early-diagnosed patients, and responses to short-term chenodeoxycholic acid (CDCA) treatment. Seven of 11 CTX patients were diagnosed in childhood. Three patients (27%) had neonatal cholestasis, seven (63%) patients had a history of frequent watery defecation started in infantile period, and eight (72.7%) patients had juvenile cataract. Four patients in the adult age group had pyramidal signs and parkinsonism symptoms. The mean Mignarri score at diagnosis was significantly lower in the pediatric patients (267.8 ± 51.4) than in the adult patients (450.0 ± 64.0, p = 0.001). No significant difference was determined between pediatric patients and adult patients regarding plasma cholestanol concentration at diagnosis (p = 0.482). The frequency of defecation decreased with treatment in six children, who had diarrhea at admission. Compared to pretreatment values, patients' body weight and standardized body mass index significantly increased at the 12th month of treatment. In conclusion, Mignarri scores are lower in the pediatric patients than in adult patients since the most determinative signs of the CTX disease are not apparent yet in the childhood. The disease is frequently overlooked in routine practice as the disease presents itself with different clinical combinations both in adults and in children. CTX is potentially a treatable disease; thereby, enhanced awareness is critically important for early diagnosis particularly in children.

Indexed as

Early DiagnosisAdolescentAdultChenodeoxycholic AcidChildCholestanolCross-Sectional StudiesFemaleHumansMaleMiddle AgedXanthomatosis, CerebrotendinousChenodeoxycholic AcidCholestanolCerebrotendinous xanthomatosisCholestanolCYP27A1Novel mutationPediatrics

Identifiers

PMID33704661
OpenAlexW3134553075

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.