1.Risk Assessment for Ramadan Fasting in People With Diabetes in Hospital-Based Diabetes Clinics Using the Updated 2026 IDF-DAR Risk Calculator
Raja Nurazni Raja Azwan ; Chin Voon Tong ; Lisa Mohamed Nor ; Marisa Khatijah Borhan ; Syarifah Syahirah Syed Abas ; Poh Shean Wong ; Ying Jie Tan ; Shartiyah Ismail ; Eunice Yi Chwen Lau ; Yueh Chien Kuan ; Noor Hafis Md Tob ; Shu Teng Chai ; Pei Lin Chan ; Xe Hui Lee ; Wei Wei Ng ; Jin Hui Ho ; Miza Hiryanti Zakaria ; Rabeah Md Zuki ; Wan Mohd Hafez Wan Hamzah ; Melissa Vergis ; Choon Peng Sun ; Vanusha Devaraja Pillai ; Chee Koon Low ; Shazatul Reza Mohd Redzuan ; Xin-Yi Ooi ; Siti Sanaa Wan Azman ; Deviga Lachumanan ; Saiful Shahrizal Shudim ; Zanariah Hussein
Journal of the ASEAN Federation of Endocrine Societies 2026;41(S1):42-43
Introduction:
The 2021 IDF-DAR risk calculator had been previously
evaluated in multiple studies and subsequently widely
accepted and applied in clinical practice as a practical
standardized tool for patient risk stratification. Recently
updated, the 2026 IDF-DAR Risk calculator enables a more individualized, evidence-related evaluation of patientrelated and disease-related risk factors, incorporating
modern diabetes technologies, including continuous
glucose monitoring (CGM), automated insulin delivery
(AID) systems, and advanced insulin formulations to
enhance risk stratification. This tool allows medical
professionals to tailor Ramadan practices based on overall
factors toward promoting safe fasting.
Methodology:
This prospective multicentre observational study recruited
adults with Type 1 and Type 2 diabetes attending public
hospitals nationwide. People with diabetes (PwD) intending
to perform Ramadan fasting were invited to participate
and assessed using the 2026 IDF-DAR Risk Calculator in
the 6-week pre-Ramadan period between 30th January and
19th March 2026.
Results:
A total of 458 PwD were evaluated and stratified into low
(15.7%), moderate (41%), and high risk (43.3%) categories.
Most participants had Type 2 diabetes (83.6%), with 60.3%
having a disease duration exceeding 10 years and 43%
exhibiting poor glycemic control (hemoglobin A1c >9%).
Insulin therapy was used by 76.4% of participants, including
two individuals with Type 1 diabetes using AID systems.
Most participants reported no recent hypoglycemia (76.4%),
81.0% performed glucose monitoring, and 3.3% used CGM.
Severe comorbidities were uncommon, with 1.1% having
unstable macrovascular disease and 4.4% advanced chronic
kidney disease (estimated glomerular filtration rate <30).
Notably, 72.2% received structured Ramadan education.
Conclusion
Majority of PwD attending tertiary diabetes clinics were
in the moderate- to high-risk category and intended to
fast despite medical advice against fasting in some cases.
Although most participants were on insulin therapy,
hypoglycemia was low in the pre-Ramadan period.
Integration of modern technologies, advanced insulin
therapies, and structured education may support safer
fasting practices.
Risk Assessment
;
Diabetes Mellitus
;
Hospitals
;
Fasting
2.Effectiveness of Oral Semaglutide Versus Injectable Dulaglutide in Adults With Type 2 Diabetes and Obesity: A Single-Centre Experience
Nur Shairah Binti Mohamad Fazial ; Raja Yunalis Binti Raja Iskandar ; Nur Syuhaida Binti Noorazam ; Saiful Shahrizal Bin Shudim
Journal of the ASEAN Federation of Endocrine Societies 2026;41(S1):43-
Introduction:
Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are
increasingly used in the management of type 2 diabetes
mellitus (T2DM) and obesity because of their glucoselowering and weight reduction benefits. However, realworld outcomes may differ from clinical trial data.
Methodology:
This retrospective cohort study included adults with T2DM
and obesity initiated on oral semaglutide or injectable
dulaglutide at Hospital Sultan Haji Ahmad Shah between
2023 and 2025. Baseline and approximately 6-month
follow-up data were obtained from electronic medical
records. Outcomes included weight, body mass index
(BMI), glycated hemoglobin A1c (HbA1c), total daily
insulin dose (TDD), low-density lipoprotein (LDL), and
gastrointestinal adverse effects. Results are presented as
median (interquartile range, IQR).
Results:
A total of 22 patients were included, with a median age of
45 years (IQR 39.3–54.5); 13 (59.1%) were male. Thirteen
patients (59.1%) received oral semaglutide and nine (40.9%)
received injectable dulaglutide. In the semaglutide group,
median HbA1c changed from 8.1% (7.4–9.1) to 8.2% (7.1–
9.3), weight from 95.4 kg (84.0–99.1) to 89.6 kg (79.0–100.0),
BMI from 33.9 kg/m² (31.4–40.8) to 33.6 kg/m² (31.2–35.6),
TDD from 64 IU/day (20–82) to 46 IU/day (18–48), and
LDL from 2.2 mmol/L (1.6–2.3) to 2.3 mmol/L (1.3–3.0).
In the dulaglutide group, median HbA1c improved from
7.6% (7.4–9.6) to 6.9% (6.5–8.4), weight from 117.0 kg
(101.0–121.0) to 111.0 kg (105.0–119.0), BMI from 41.0 kg/
m² (40.0–49.0) to 42.5 kg/m² (38.0–48.0), TDD from 33 IU/
day (30.5–34.0) to 34 IU/day (30.5–34.0), and LDL from 2.2
mmol/L (1.8–2.9) to 2.6 mmol/L (2.0–4.0). Gastrointestinal
side effects occurred in 4/13 (30.8%) oral semaglutide users
and 0/9 dulaglutide users.
Conclusion
Injectable dulaglutide showed greater improvement in
HbA1c, while both groups demonstrated variable effects
on weight, BMI, insulin requirement, and LDL in routine
practice.
Adult
;
dulaglutide
;
semaglutide
;
Diabetes Mellitus, Type 2
;
Obesity


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