Evidence map›Paper›PMID 35315383›Full record

ArticleActa bio-medica : Atenei Parmensis2022

Screening for glucose dysregulation in β-thalassemia major (β-TM): An update of current evidences and personal experience.

Vincenzo De Sanctis, Shahina Daar, Ashraf T Soliman, Ploutarchos Tzoulis, Mehran Karimi, Salvatore Di Maio, Christos Kattamis

Open access · greenAbstract read
In one paragraph

Article in Acta bio-medica : Atenei Parmensis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 16 citations in OpenAlex.

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  11. Endocrinopathies in Hemoglobinopathies: What Is the Role of Iron?International journal of molecular sciences · 2023
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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

7 authors at 7 institutions in 6 countries.

Vincenzo De SanctisQuisisana Hospital, Ferrara. vdesanctis@libero.it.
Shahina DaarDepartment of Haematology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Sultanate of Oman. sf.daar@gmail.com.
Ashraf T SolimanDepartment of Pediatrics, Division of Endocrinology, Hamad General Hospital, Doha, Qatar and Department of Pediatrics, Division of Endocrinology, Alexandria University Children's Hospital, Alexandria, Egypt. atsoliman56@gmail.com.
Ploutarchos TzoulisDepartment of Diabetes and Endocrinology, Whittington Hospital, University College London, London, UK. ptzoulis@yahoo.co.uk.
Mehran KarimiHematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. mkarimi820@gmail.com.
Salvatore Di MaioEmeritus Director in Pediatrics, Children's Hospital "Santobono-Pausilipon", Naples, Italy . dimaiosalvatore@tin.it.
Christos KattamisFirst Department of Paediatrics, National Kapodistrian University of Athens 11527, Greece. christos.kattamis@gmail.com.
Arcispedale Sant'Anna · ITHamad General Hospital · QANational and Kapodistrian University of Athens · GRSantobono Children's Hospital · ITShiraz University of Medical Sciences · IRSultan Qaboos University · OMWhittington Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucose dysregulation (GD) in patients with β-thalassemia major (β-TM) usually develops gradually. Prediabetes consists of two abnormalities, impaired fasting glucose (IFG) and impaired glucose tolerance (IGT), the latter detected by a standardized oral glucose tolerance test (OGTT). Diagnosis of prediabetes is essential for an early identification of high-risk individuals who will benefit from intensive iron chelation therapy and lifestyle modification. Therefore, patients with β-TM should undergo annual screening for glucose abnormalities, according to international recommendations, starting from the age of 10 years. OGTT remains the preferred screening method as it is more sensitive for GD than fasting plasma glucose (FPG), although it is poorly reproducible. The use of HbA1c measurement has limited use as it is generally considered unreliable in patients with thalassemia. Continuous glucose monitoring system (CGMS) is an accurate method to detect the variability of glucose fluctuations and offers the opportunity for better assessment of glucose homeostasis in a selected group of β-TM patients. Pancreatic Magnetic Resonance Imaging (MRI) associated with insulin secretion-sensitivity index-2 (ISSI-2) could be a complementary test, minimizing the necessity for OGTT and identifying high-risk patients before irreversible pancreatic damage occurs. The aims of this short report are to give practical guidance for an early identification of GD in β-TM patients, to summarise our experience, and to offer an impetus for further research in the field.

Indexed as

beta-ThalassemiaPrediabetic StateBlood GlucoseBlood Glucose Self-MonitoringChildGlucoseHumansBlood GlucoseGlucose

Identifiers

PMID35315383
PMCPMC8972848
OpenAlexW4221013800

What OpenQuestion holds

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LicenceCC BY-NC
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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.