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The Association of Nonalcoholic Fatty Liver Disease with Subclinical Atherosclerosis: A Systematic Review Caroline Johansyah; I Putu Oka Yudaswara Pande; Maria Johansyah
The International Journal of Medical Science and Health Research Vol. 18 No. 5 (2025): 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/fx8vy119

Abstract

Introduction: Nonalcoholic Fatty Liver Disease (NAFLD) has emerged as a global public health issue, increasingly recognized for its strong association with cardiovascular disease (CVD), the leading cause of mortality in this patient population. This systematic review aims to comprehensively evaluate and synthesize the evidence linking NAFLD to a wide array of markers for subclinical atherosclerosis, the earliest detectable stage of CVD. Methods: A systematic search of PubMed, Google Scholar, Semantic Scholar, Springer, Wiley Online Library databases was conducted for observational studies investigating the association between NAFLD and subclinical atherosclerosis. The review adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Included studies were assessed for methodological quality using the Newcastle-Ottawa Scale (NOS). Results: Synthesis of data from 17 selected high-quality observational studies, encompassing tens of thousands of participants, revealed a consistent and statistically significant association between NAFLD and multiple indices of subclinical atherosclerosis. Specifically, NAFLD was linked to increased carotid intima-media thickness (CIMT), a higher prevalence of carotid plaques, elevated coronary artery calcification (CAC) scores, and accelerated CAC progression. Furthermore, NAFLD was associated with significant functional vascular impairments, including endothelial dysfunction (manifested as reduced flow-mediated dilation) and increased arterial stiffness (measured by pulse wave velocity). These associations frequently persisted after adjustment for traditional metabolic risk factors. Discussion: The findings support the biological plausibility of NAFLD as an active contributor to atherogenesis, not merely a passive bystander. Shared pathophysiological mechanisms, including systemic inflammation, insulin resistance, and atherogenic dyslipidemia, likely drive this liver-vessel axis. The presence of NAFLD may serve as a clinical risk enhancer, identifying individuals with a heightened burden of subclinical vascular disease who might be missed by conventional risk scoring. Conclusion: NAFLD is a robust indicator for the presence of multi-site subclinical atherosclerosis. These findings underscore the importance of cardiovascular surveillance and aggressive risk factor management in individuals diagnosed with NAFLD to mitigate the long-term risk of cardiovascular events.
The Association of Diabetes Mellitus with Premature Coronary Artery Disease: A Systematic Review of Pathophysiology, Biomarkers, and Clinical Outcomes Caroline Johansyah; I Putu Oka Yudaswara Pande; Maria Johansyah
The International Journal of Medical Science and Health Research Vol. 18 No. 5 (2025): 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/mqkn4q79

Abstract

Introduction: Premature Coronary Artery Disease (PCAD), defined as atherosclerotic cardiovascular disease in young adults, represents a significant and escalating public health challenge with profound socioeconomic consequences. Diabetes Mellitus (DM) is recognized as a principal and potent risk factor for cardiovascular disease, yet the full spectrum of its association with the aggressive phenotype of PCAD requires a comprehensive synthesis of the available evidence. This systematic review aims to elucidate the multifaceted relationship between DM and PCAD, spanning from pathophysiology to clinical outcomes. Methods: This systematic review was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A comprehensive search of PubMed, Google Scholar, Semantic Scholar, Springer, Wiley Online Library databases was performed to identify observational studies (cohort and case-control) examining the association between DM, prediabetes, or insulin resistance and PCAD. The methodological quality and risk of bias of included studies were rigorously assessed using the Newcastle-Ottawa Scale (NOS). A qualitative synthesis of the evidence was performed. Results: A total of 18 studies met the inclusion criteria. The evidence demonstrates a high prevalence of both diagnosed and previously undiagnosed DM in PCAD cohorts, often exceeding 30%. DM was significantly and consistently associated with increased angiographic severity, including a higher burden of multivessel disease and higher complexity scores. Clinically, DM emerged as a powerful independent predictor of adverse outcomes. Patients with PCAD and concomitant DM experience substantially higher rates of Major Adverse Cardiovascular Events (MACE), all-cause mortality, cardiovascular mortality, and recurrent myocardial infarction compared to their non-diabetic counterparts. Furthermore, novel biomarkers of insulin resistance, such as the Metabolic Score for Insulin Resistance (METS-IR) and the Triglyceride-Glucose (TyG) index, demonstrated superior predictive power for MACE over traditional metabolic markers. Discussion: The synthesized findings indicate that DM functions as a critical disease accelerator in the context of PCAD. The underlying pathophysiology, driven by insulin resistance and chronic hyperglycemia, fosters a systemic pro-inflammatory and pro-thrombotic state that promotes a more aggressive and diffuse atherosclerotic phenotype. The clinical implications are profound, highlighting a critical need for earlier risk stratification using novel biomarkers and more aggressive, multifactorial risk reduction strategies in young adults with metabolic dysfunction. Conclusion: The evidence robustly confirms that Diabetes Mellitus is a fundamental determinant of the risk, severity, and poor prognosis associated with Premature Coronary Artery Disease. This warrants a paradigm shift in clinical practice towards the early detection of insulin resistance and the implementation of intensive, secondary prevention-level care for young adults with DM to mitigate their substantial long-term cardiovascular risk.
The Association of Vitamin D Deficiency with Disease Activity in Rheumatoid Arthritis: A Systematic Review Caroline Johansyah; I Putu Oka Yudaswara Pande; Maria Johansyah
The International Journal of Medical Science and Health Research Vol. 18 No. 6 (2025): 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: 10.70070/01pf3g54

Abstract

Introduction: Rheumatoid Arthritis (RA) is a chronic, systemic autoimmune disease characterized by persistent synovitis. Vitamin D, a secosteroid hormone with potent immunomodulatory properties, is frequently observed to be deficient in this patient population. This systematic review aims to comprehensively evaluate and synthesize the evidence linking vitamin D deficiency to the multifaceted measures of disease activity in RA. Methods: A systematic literature search was conducted across PubMed, Google Scholar, Semantic Scholar, Springer, Wiley Online Library for observational studies published up to December 2024. Studies were included if they assessed serum 25-hydroxyvitamin D levels and at least one validated measure of disease activity in adult patients with RA. Data on study characteristics and over 15 distinct clinical, laboratory, and patient-reported outcomes were extracted. The methodological quality and risk of bias of included studies were assessed using the Cochrane ROBINS-I (Risk Of Bias In Non-randomized Studies – of Interventions) tool. Results: Seventeen observational studies, comprising a total of 5,618 RA patients, met the inclusion criteria. The findings revealed a high prevalence of vitamin D deficiency and insufficiency across diverse RA cohorts. A statistically significant inverse correlation between serum 25(OH)D levels and the Disease Activity Score in 28 joints (DAS28) was the most consistent finding across the majority of studies. Furthermore, lower vitamin D levels were significantly associated with higher levels of inflammatory markers, including Erythrocyte Sedimentation Rate (ESR) and C-Reactive Protein (CRP), increased tender and swollen joint counts, and worse patient-reported outcomes such as pain, functional disability (Health Assessment Questionnaire), and reduced quality of life. Discussion: The synthesized evidence strongly supports an association between lower vitamin D status and heightened disease activity in RA. This relationship is biologically plausible, given vitamin D's established role in suppressing pro-inflammatory Th1/Th17 pathways and promoting regulatory T-cell function, both of which are central to RA pathogenesis. While the cross-sectional nature of most studies precludes definitive causal inference, the data suggest a potential bidirectional relationship where deficiency may contribute to immune dysregulation, and active disease may in turn exacerbate the deficiency. Conclusion: A substantial body of evidence demonstrates a significant association between vitamin D deficiency and higher disease activity across multiple domains in RA. These findings underscore the clinical importance of monitoring and correcting vitamin D status in patients with RA, which may serve as a valuable, low-cost adjunct to standard therapeutic strategies to help mitigate the overall disease burden.