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The Comprehensive Systematic Review of Association of the HLA-B27 antigen to the development of ankylosing spondylitis Clareta Vero Patricia Widya; Devina Adelina Wijaya
The International Journal of Medical Science and Health Research Vol. 25 No. 1 (2026): The International Journal of Medical Science and Health Research
Publisher : International Medical Journal Corp. Ltd

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.70070/vnecfx77

Abstract

Introduction: Ankylosing Spondylitis (AS) is a chronic inflammatory arthritis primarily affecting the axial skeleton, with a well-established but complex genetic association with the Human Leukocyte Antigen B27 (HLA-B27). Despite decades of research, the precise mechanisms, the differential roles of HLA-B27 subtypes, and the influence of geographic and genetic modifiers remain areas of active investigation (Reveille, 2006). Methods: This comprehensive systematic review synthesized evidence from 80 studies, including case-control studies, cohort studies, and meta-analyses. A stringent screening process was applied, focusing on studies with defined AS diagnostic criteria, confirmed HLA-B27 testing, comparison groups, and reported statistical measures of association. Data extraction covered study design, population characteristics, HLA-B27 testing methods, AS definitions, association results (odds ratios, relative risks), HLA-B27 prevalence, subtype analyses, epistatic interactions, and clinical phenotype correlations. Results: The analysis confirmed an exceptionally strong association between HLA-B27 and AS, with relative risks estimated between 50 and 100 for carriers. However, significant heterogeneity exists. HLA-B27 prevalence in AS patients varies geographically, from ~90% in Caucasian and Asian populations to as low as 26.2% in some Middle Eastern countries. Critical nuances emerged: specific subtypes confer differential risk (e.g., B2704 is a risk factor, while B2706 and B*2707 are protective), and powerful epistatic interactions were identified, particularly with HLA-B60 (RR up to 342) and ERAP1 polymorphisms. Clinically, HLA-B27 positivity is associated with earlier disease onset, better response to biologic therapies, and shorter diagnostic delays, but a lower-than-expected diagnostic likelihood ratio (LR+ 2.7) (A. D. Vieira Bento Silva et al., 2023). Discussion: The findings underscore that HLA-B27 is a necessary but insufficient factor for AS pathogenesis. The disease risk is modulated by a complex interplay of specific HLA-B27 subtypes, co-inherited genetic factors (epistasis), and population-specific genetic backgrounds. This complexity explains why only 1-5% of HLA-B27 carriers develop AS and accounts for the wide geographic variation in disease association strength. Conclusion: HLA-B27 remains the paramount genetic risk factor for AS, but its clinical and pathogenic interpretation must account for subtype variation, epistatic interactions, and ethnic background. Future research should prioritize elucidating the molecular mechanisms of protective subtypes and integrating polygenic risk scores with HLA status for improved diagnosis, prognosis, and personalized treatment strategies.
The Comprehensive Systematic Review of Association of Non-Nutritive Sweetener Consumption to Potential Effects of Glucose Intolerance Devina Adelina Wijaya; Clareta Vero Patricia Widya
The International Journal of Medical Science and Health Research Vol. 25 No. 1 (2026): The International Journal of Medical Science and Health Research
Publisher : International Medical Journal Corp. Ltd

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.70070/z329kc27

Abstract

Introduction: Non-nutritive sweeteners (NNS) are widely used as sugar substitutes to reduce caloric intake and manage body weight, yet their long-term metabolic effects, particularly on glucose tolerance, remain controversial. While acute studies often report neutral effects, emerging evidence suggests that chronic consumption, especially of certain NNS types, may adversely affect insulin sensitivity and glucose homeostasis in specific populations (Romo-Romo et al., 2018; Suez et al., 2022). Methods: A comprehensive systematic review was conducted, screening studies based on predefined inclusion criteria: human participants, NNS exposure assessment, glucose metabolism outcomes, appropriate study designs (RCTs, cohort studies, systematic reviews), and methodological quality. Data extraction covered NNS type, dosage, study population, glucose outcomes, study design, key findings, and proposed mechanisms. A total of 80 studies were included and critically synthesized. Results: The evidence reveals significant heterogeneity in NNS effects. Acute NNS exposure generally has minimal impact on postprandial glucose and insulin (Greyling et al., 2020), but chronic consumption (≥2 weeks), particularly of sucralose, is associated with decreased insulin sensitivity in healthy, lean, non-habitual users (Romo-Romo et al., 2018, 2024, 2025). Effects vary by sweetener type: stevia shows neutral to beneficial effects on fasting glucose (Bai et al., 2024; Zare et al., 2024), aspartame largely exhibits neutral metabolic impact (Santos et al., 2018; Higgins et al., 2018), while saccharin and sucralose demonstrate more variable, often microbiome-dependent outcomes (Suez et al., 2022; Méndez-García et al., 2022). Population characteristics, including baseline metabolic health and habitual NNS use, significantly moderate these effects. Discussion: The divergence in findings can be explained by population-specific responses, sweetener-specific mechanisms (e.g., gut microbiota modulation by sucralose), study duration, methodological quality, and comparator substances. When NNS replace sugar-sweetened beverages, they generally offer a net metabolic benefit, supporting their role in dietary strategies for sugar reduction (McGlynn et al., 2020; Lee et al., 2022). Conclusion: The impact of NNS on glucose metabolism is not uniform but is influenced by sweetener type, consumption duration, and individual host factors such as metabolic health and gut microbiome composition. While certain NNS may pose risks to insulin sensitivity in metabolically naive individuals, they remain a preferable alternative to caloric sweeteners for weight and glycemic management in broader populations. Future research should focus on personalized nutrition approaches and long-term outcomes.