The frequency of Duchenne muscular dystrophy/Becker muscular dystrophy and Pompe disease in children with isolated transaminase elevation: results from the observational VICTORIA study.

Becker muscular dystrophy Duchenne muscular dystrophy Pompe disease elevated transaminase hypertransaminasemia neuromuscular disease

Journal

Frontiers in pediatrics
ISSN: 2296-2360
Titre abrégé: Front Pediatr
Pays: Switzerland
ID NLM: 101615492

Informations de publication

Date de publication:
2023
Historique:
received: 03 08 2023
accepted: 01 09 2023
medline: 11 10 2023
pubmed: 11 10 2023
entrez: 11 10 2023
Statut: epublish

Résumé

Elevated transaminases and/or creatine phosphokinase can indicate underlying muscle disease. Therefore, this study aims to determine the frequency of Duchenne muscular dystrophy/Becker muscular dystrophy (DMD/BMD) in male children and Pompe disease (PD) in male and female children with isolated hypertransaminasemia. This multi-center, prospective study enrolled patients aged 3-216 months with serum alanine transaminase (ALT) and/or aspartate transaminase (AST) levels >2× the upper limit of normal (ULN) for ≥3 months. Patients with a known history of liver or muscle disease or physical examination findings suggestive of liver disease were excluded. Patients were screened for creatinine phosphokinase (CPK) levels, and molecular genetic tests for DMD/BMD in male patients and enzyme analysis for PD in male and female patients with elevated CPK levels were performed. Genetic analyses confirmed PD. Demographic, clinical, and laboratory characteristics of the patients were analyzed. Overall, 589 patients [66.8% male, mean age of 63.4 months (standard deviation: 60.5)] were included. In total, 251 patients (188 male and 63 female) had CPK levels above the ULN. Of the patients assessed, 47% (85/182) of male patients were diagnosed with DMD/BMD and 1% (3/228) of male and female patients were diagnosed with PD. The median ALT, AST, and CPK levels were statistically significantly higher, and the questioned neurological symptoms and previously unnoticed examination findings were more common in DMD/BMD patients than those without DMD/BMD or PD ( Questioning neurological symptoms, conducting a complete physical examination, and testing for CPK levels in patients with isolated hypertransaminasemia will prevent costly and time-consuming investigations for liver diseases and will lead to the diagnosis of occult neuromuscular diseases. Clinicaltrials.gov NCT04120168.

Identifiants

pubmed: 37818166
doi: 10.3389/fped.2023.1272177
pmc: PMC10560724
doi:

Banques de données

ClinicalTrials.gov
['NCT04120168']

Types de publication

Journal Article

Langues

eng

Pagination

1272177

Investigateurs

Didem Gülcü Taşkın (DG)
Ayşegül Bükülmez (A)
Arzu Meltem Demir (AM)
Yavuz Tokgöz (Y)
Aydan Kansu (A)
Zarife Kuloğlu (Z)
Ceyda Tuna Kırsaçlıoğlu (CT)
Hasret Ayyıldız (H)
Günsel Kutluk (G)
Meryem Keçeli Başaran (MK)
Oya Balcı Sezer (OB)
Tanju Başarır Özkan (TB)
Taner Özgür (T)
Gonca Handan Üstündağ (GH)
Eda Somuncu (E)
Gökhan Tümgör (G)
Sibel Yavuz (S)
Ali İşlek (A)
Ferda Özbay Hoşnut (FÖ)
Gülseren Evirgen Şahin (GE)
Duran Arslan (D)
Derya Altay (D)
Yaşar Doğan (Y)
Uğur Deveci (U)
Buket Dalgıç (B)
Kamercan Ceylan (K)
Ahmet Baştürk (A)
Necati Balamtekin (N)
Melike Arslan (M)
Hülya Demir (H)
Hayriye Hızarcıoğlu Gülşen (HH)
Güzide Doğan (G)
Atakan Comba (A)
Mukadder Ayşe Selimoğlu (MA)
İlknur Varol (İ)
Sebahat Çam (S)
Eylem Sevinç (E)
Erkan Doğan (E)
Murat Çakır (M)
Burcu Güven (B)
Suna Selbuz (S)
Hacer Fulya Gülerman (HF)
Zeynep Arslan (Z)
Ayşen Uncuoğlu (A)
Neslihan Gürcan Kaya (NG)
Deniz Ertem (D)
Engin Tutar (E)
Burcu Volkan (B)
Yasin Şahin (Y)
Yusuf Usta (Y)
Asuman Nur Karhan (AN)
Gönül Çaltepe (G)
İbrahim Ethem Taşkaya (İE)
Halil Kocamaz (H)
Tuğba Gürsoy Koca (TG)
Fatih Ünal (F)
Birol Öztürk (B)
Cansu Altuntaş (C)
Halil Haldun Emiroğlu (HH)
Meltem Gümüş (M)
Mustafa Akçam (M)
Yeliz Çağan Appak (YÇ)
Betül Aksoy (B)
Elif Sağ (E)
İshak Abdurrahman Işık (İA)
Ulaş Emre Akbulut (UE)
Özlem Bekem (Ö)
Cahit Barış Erdur (CB)
Nafiye Urgancı (N)
Ayşe Merve Usta (AM)
Coşkun Çeltik (C)
Nelgin Gerenli (N)
Nevzat Aykut Bayrak (NA)
Kaan Demirören (K)

Informations de copyright

© 2023 Kansu, Kuloglu, Tümgör, Taşkın, Dalgiç, Çaltepe, Demirören, Doğan, Tuna Kırsaçlıoğlu, Arslan, Işık, Demir, Bekem, Şahin, Bayrak, Selimoğlu, Yavuz, Taşkaya and Altay and the VICTORIA Study Group.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

Curr Opin Neurol. 2019 Oct;32(5):722-727
pubmed: 31343429
Lancet Neurol. 2018 Mar;17(3):251-267
pubmed: 29395989
J Am Board Fam Med. 2012 Jul-Aug;25(4):536-40
pubmed: 22773723
Am Fam Physician. 2017 Dec 1;96(11):709-715
pubmed: 29431403
Nutrients. 2022 Aug 12;14(16):
pubmed: 36014811
Orphanet J Rare Dis. 2020 Apr 5;15(1):83
pubmed: 32248831
Postgrad Med J. 2003 Jun;79(932):307-12
pubmed: 12840117
J Pediatr. 2010 Apr;156(4):689
pubmed: 20138302
Orphanet J Rare Dis. 2020 Jun 5;15(1):141
pubmed: 32503598
ACG Case Rep J. 2016 Jan 20;3(2):127-9
pubmed: 26958568
Pediatrics. 2011 Jan;127(1):e132-6
pubmed: 21149430
J Paediatr Child Health. 2012 Oct;48(10):886-90
pubmed: 20500440
J Pediatr Gastroenterol Nutr. 2011 Oct;53(4):463-4
pubmed: 21970998
Lancet Neurol. 2018 May;17(5):445-455
pubmed: 29398641
Curr Treat Options Neurol. 2022 Nov;24(11):573-588
pubmed: 36969713
Neuromuscul Disord. 2023 Jun;33(6):476-483
pubmed: 37207382
Neurol Clin. 2014 Aug;32(3):751-76, ix
pubmed: 25037089
Am Fam Physician. 2005 Mar 15;71(6):1105-10
pubmed: 15791889
Dis Markers. 2015;2015:543282
pubmed: 26063958

Auteurs

Aydan Kansu (A)

Department of Pediatrics, Division of Pediatric Gastroenterology, Ankara University School of Medicine, Ankara, Türkiye.

Zarife Kuloglu (Z)

Department of Pediatrics, Division of Pediatric Gastroenterology, Ankara University School of Medicine, Ankara, Türkiye.

Gökhan Tümgör (G)

Department of Pediatric Gastroenterology, Çukurova University School of Medicine, Adana, Türkiye.

Didem Gülcü Taşkın (DG)

Department of Pediatrics, Adana City Training and Research Hospital, Adana, Türkiye.

Buket Dalgıç (B)

Department of Pediatric Gastroenterology, Gazi University School of Medicine, Ankara, Türkiye.

Gönül Çaltepe (G)

Department of Pediatric Gastroenterology, Ondokuz Mayıs University School of Medicine, Samsun, Türkiye.

Kaan Demirören (K)

Department of Pediatrics, Yüksek İhtisas Training and Research Hospital, Bursa, Türkiye.

Güzide Doğan (G)

Department of Pediatrics, Haseki Training and Research Hospital, İstanbul, Bezmialem Vakıf University, İstanbul, Türkiye.

Ceyda Tuna Kırsaçlıoğlu (C)

Department of Pediatrics, Division of Pediatric Gastroenterology, Ankara University School of Medicine, Ankara, Türkiye.

Duran Arslan (D)

Department of Pediatric Gastroenterology, Erciyes University School of Medicine, Kayseri, Türkiye.

İshak Abdurrahman Işık (İA)

Department of Pediatrics, University of Health Sciences Antalya Training and Research Hospital, Antalya, Türkiye.

Hülya Demir (H)

Department of Pediatric Gastroenterology, Hacettepe University School of Medicine, Ankara, Türkiye.

Özlem Bekem (Ö)

University of Health Sciences, Dr. Behçet Uz Children's Hospital, İzmir, Türkiye.

Yasin Şahin (Y)

Department of Pediatrics, Mersin City Training and Research Hospital, Mersin, Türkiye.

Nevzat Aykut Bayrak (NA)

University of Health Sciences, Zeynep Kamil Women and Children's Training and Research Hospital, İstanbul, Türkiye.

Mukadder Ayşe Selimoğlu (MA)

Department of Pediatric Gastroenterology, İnönü University School of Medicine, Malatya, Türkiye.

Sibel Yavuz (S)

Department of Pediatric Gastroenterology, Çukurova University School of Medicine, Adana, Türkiye.

İbrahim Ethem Taşkaya (İE)

Department of Pediatric Gastroenterology, Ondokuz Mayıs University School of Medicine, Samsun, Türkiye.

Derya Altay (D)

Department of Pediatric Gastroenterology, Erciyes University School of Medicine, Kayseri, Türkiye.

Classifications MeSH