Akhtar Saeed, Muzaini Hadeel El, Al-Hashel Jasem Y, Alroughani Raed
Department of Community Medicine and Behavioural Sciences, College of Medicine, Kuwait University, PO Box 24923, Safat, 13110, Kuwait.
Department of Medicine, College of Medicine, Kuwait University, PO Box 24923, Safat, 13110, Kuwait.
Neurol Sci. 2025 Apr 22. doi: 10.1007/s10072-025-08187-7.
This study aimed to quantify the population attributable (or prevented) fraction (PAR or PPF) of common risk factors for multiple sclerosis (MS) including family history of MS and vaccine uptake against influenza A and B viruses and hepatitis B virus.
Confirmed MS cases and MS-free controls pair-matched on age (± 5 years), sex and nativity with cases were enrolled. Data were collected through face-to-face interviews both from the cases and controls. An unconditional multivariable logistic regression model was used to analyze the data by including matching factors i.e., age, sex, and nativity as confounders and MS family history and vaccine uptake against influenza viruses and hepatitis B virus as exposures. The adjusted odds ratios and their 95% confidence intervals (CI) were used to compute PAR for family history of MS and PPFs for vaccine uptake against HBV and influenza virus along with their respective 95% CIs.
A total of 110 MS cases, and their 110 pair-matched controls were enrolled. The PAF for family history of MS revealed that 22% of MS risk in the population is contributed by family history of MS (PAF = 0.22; 95% CI: 0.10-0.32). The PPFs for vaccination uptake against influenza viruses and/or hepatitis B virus were associated with a significant nonspecific protection against MS risk by 20% (PPF = 0.20; 95% CI: 0.004-0.43) or 30% (PPF = 0.30; 95% CI: 0.03-0.65) respectively. Moreover, the computed joint PPF for vaccination uptake against influenza viruses and hepatitis B virus showed a significantly increased 44% non-specific protection against MS risk (PPF = 0.44; 95% CI: 0.03-0.80).
Familial history of MS is associated with 22% population attributable fraction for MS risk, whereas vaccine uptake against influenza viruses or hepatitis B virus conferred a nonspecific protection with population prevented fractions of 20% and 30% respectively suggesting a substantial potential for public health interventions to minimize MS risk in this and other similar settings.
本研究旨在量化多发性硬化症(MS)常见风险因素的人群归因(或预防)分数(PAR或PPF),这些因素包括MS家族史以及甲型和乙型流感病毒及乙型肝炎病毒疫苗接种情况。
纳入确诊的MS病例以及在年龄(±5岁)、性别和出生地与病例匹配的无MS对照。通过面对面访谈收集病例和对照的数据。使用无条件多变量逻辑回归模型分析数据,将匹配因素(即年龄、性别和出生地)作为混杂因素,将MS家族史以及甲型和乙型流感病毒及乙型肝炎病毒疫苗接种情况作为暴露因素。调整后的优势比及其95%置信区间(CI)用于计算MS家族史的PAR以及乙型肝炎病毒和流感病毒疫苗接种的PPF及其各自的95%CI。
共纳入110例MS病例及其110例匹配对照。MS家族史的PAF显示,人群中22%的MS风险由MS家族史导致(PAF = 0.22;95%CI:0.10 - 0.32)。接种甲型和/或乙型流感病毒疫苗的PPF与MS风险的显著非特异性保护相关,分别为20%(PPF = 0.20;95%CI:0.004 - 0.43)或30%(PPF = 0.30;95%CI:0.03 - 0.65)。此外,接种甲型和乙型流感病毒及乙型肝炎病毒疫苗的联合PPF显示,对MS风险的非特异性保护显著增加44%(PPF = 0.44;95%CI:0.03 - 0.80)。
MS家族史与MS风险的22%人群归因分数相关,而接种甲型和乙型流感病毒或乙型肝炎病毒疫苗分别提供了20%和30%的人群预防分数的非特异性保护,这表明在本研究及其他类似情况下,公共卫生干预措施在将MS风险降至最低方面具有巨大潜力。