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Incidence of Tuberculosis Among Immigrants in Korea Who Participated in a Latent Tuberculosis Infection Screening Program. 参加潜伏肺结核感染筛查计划的韩国移民的肺结核发病率。
IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-07-22 DOI: 10.3346/jkms.2024.39.e207
Yoo Jung Lee, Jinsoo Min, Jun-Pyo Myong, Yun-Hee Lee, Young-Joon Park, Yujin Kim, Gahee Kim, Gyuri Park, Sung-Soon Lee, Jae Seuk Park, Ju Sang Kim, Hyung Woo Kim

Background: With a rapid decrease in tuberculosis (TB) incidence, the significance of latent tuberculosis infection (LTBI) has been underscored in South Korea. Although South Korea does not have a high proportion of immigrants compared to other countries, there is a growing argument that it should actively embrace immigrants as a solution to address issues of low birth rates and population aging. This study aimed to assess TB incidence among immigrants who participated a pilot LTBI screening program in South Korea.

Methods: Records of immigrants participated in a pilot LTBI screening program in South Korea between 2018 and 2019 were linked with Korean National TB Surveillance System to determine TB development. Participants underwent interferon-gamma release assay (IGRA) and chest X-rays. Standardized incidence ratios (SIRs) stratified by age, country of origin's TB burden was calculated with a reference group of general South Korean population.

Results: Of a total of 9,517 participants, 14 TB cases were identified. Participants with positive IGRA results who did not initiate LTBI treatment showed TB incidence of 312.5 per 100,000 person-years, whereas those with negative results showed TB incidence of 34.4 per 100,000 person-years, resulting in an incidence rate ratio of 9.08 (95% confidence interval [CI], 2.50-32.99). SIR of TB among total participants including those with negative IGRA results was 2.60 (95% CI, 1.54-4.38; P < 0.001), whereas SIR among those with positive IGRA results was 5.86 (95% CI, 3.15-10.89; P < 0.001). In the calculation of SIR among participants with positive IGRA results, those aged under 35 from high TB-burden countries or intermediate TB-burden countries showed a high SIR (18.08; 95% CI, 2.55-128.37; P = 0.004), and 11.30 (95% CI, 2.82-45.16; P < 0.001), respectively). Contrary to previous reports that suggest the majority of elderly population with a positive IGRA result were due to remote infection and had a lower TB risk compared to younger ages, SIR among those aged 65 or over from intermediate TB-burden countries was 6.15 (95% CI, 0.87-43.69; P = 0.069), which was comparable to that in younger participants aged between 35 and 49 (SIR, 4.87; 95% CI, 1.22-19.49; P = 0.025) or those aged between 50 and 64 (SIR, 4.62; 95% CI, 1.73-12.31; P = 0.002).

Conclusion: Young immigrants with positive IGRA results from countries with high or intermediate TB burden showed a relatively high TB risk compared to a general South Korea population. In addition, unexpected high TB risk was observed among elderly immigrants with positive IGRA results. In establishing future policies for LTBI in immigrants in South Korea, screenings should primarily focus on younger age group (who aged under 35). Additionally, further research is needed on the high TB risk observed in elderly immigrants.

背景:随着肺结核(TB)发病率的迅速下降,潜伏肺结核感染(LTBI)的重要性在韩国得到了强调。虽然与其他国家相比,韩国的移民比例并不高,但越来越多的人认为韩国应积极接纳移民,以此来解决出生率低和人口老龄化的问题。本研究旨在评估参与韩国 LTBI 筛查试点项目的移民中的结核病发病率:将2018年至2019年期间参加韩国LTBI筛查试点项目的移民记录与韩国国家结核病监测系统相连接,以确定结核病的发展情况。参与者接受了干扰素-γ释放测定(IGRA)和胸部X光检查。以韩国普通人群为参照组,计算了按年龄、原籍国结核病负担分层的标准化发病率(SIRs):在 9517 名参与者中,共发现了 14 例肺结核病例。IGRA 结果呈阳性且未开始 LTBI 治疗的参与者的肺结核发病率为每 10 万人年 312.5 例,而结果呈阴性的参与者的肺结核发病率为每 10 万人年 34.4 例,发病率比为 9.08(95% 置信区间 [CI],2.50-32.99)。包括 IGRA 阴性结果在内的所有参与者的结核病发病率 SIR 为 2.60 (95% CI, 1.54-4.38; P < 0.001),而 IGRA 阳性结果参与者的 SIR 为 5.86 (95% CI, 3.15-10.89; P < 0.001)。在计算 IGRA 结果呈阳性的参与者的 SIR 时,来自结核病高负担国家或中等结核病负担国家的 35 岁以下参与者的 SIR 较高(分别为 18.08(95% CI,2.55-128.37;P = 0.004)和 11.30(95% CI,2.82-45.16;P < 0.001))。以前有报告称,大多数 IGRA 结果呈阳性的老年人是由于远距离感染所致,与年轻人相比,他们的结核病风险较低,与此相反,来自结核病负担中等国家的 65 岁或以上老年人的 SIR 为 6.15(95% CI,0.87-43.69;P = 0.069),与 35-49 岁的年轻参与者(SIR,4.87;95% CI,1.22-19.49;P = 0.025)或 50-64 岁的参与者(SIR,4.62;95% CI,1.73-12.31;P = 0.002)相当:结论:与韩国普通人群相比,来自结核病负担较重或中等的国家、IGRA 结果呈阳性的年轻移民患结核病的风险相对较高。此外,在 IGRA 结果呈阳性的老年移民中也发现了意想不到的高结核病风险。在制定针对韩国移民的未来迟发性肺结核政策时,筛查应主要针对年轻群体(35 岁以下)。此外,还需要进一步研究在老年移民中观察到的高结核病风险。
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引用次数: 0
Genotype Analysis of Respiratory Syncytial Virus Before and After the COVID-19 Pandemic Using Whole-Genome Sequencing: A Prospective, Single-Center Study in Korea From 2019 to 2022. 利用全基因组测序对 COVID-19 大流行前后的呼吸道合胞病毒进行基因型分析:2019年至2022年韩国前瞻性单中心研究》。
IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-07-22 DOI: 10.3346/jkms.2024.39.e206
Bonhyang Na, Yu Jin Park, Jieun Seo, Miri Park, Jee Yeon Baek, Ji Young Lee, Minyoung Kim, Jong Gyun Ahn, Seung Tae Lee, Ji-Man Kang

Background: Respiratory syncytial virus (RSV), a highly transmissible virus, is the leading cause of lower respiratory tract infections. We examined molecular changes in the RSV genome before and after the coronavirus disease 2019 (COVID-19) pandemic in Korea, and investigated whether drug-resistant mutations were present.

Methods: In this prospective, single-center study, RSV-positive respiratory samples were collected between September 2019 and December 2022. Long-read whole-genome sequencing (WGS) was performed, and the presence of known drug-resistant substitutions for palivizumab, nirsevimab, and suptavumab was investigated.

Results: Overall, 288 respiratory samples were collected from 276 children. WGS data were available for 133 samples (71 and 62 samples from the pre- and post-pandemic periods, respectively). All RSV-A strains (n = 56) belonged to the GA2.3.5 (ON1) genotype, whereas all RSV-B strains (n = 77) belonged to the GB5.0.5a (BA) genotype. No significant differences in genotypes were observed between the pre- and post-pandemic periods. In addition, no notable mutations related to nirsevimab or palivizumab resistance were detected in the F gene. However, the L172Q and S173L substitutions, which are known to confer resistance to suptavumab, were present in all RSV-B samples.

Conclusion: Despite the unprecedented interruption of RSV seasonality, there were no significant molecular changes in circulating RSV strains in Korea related to nirsevimab or palivizumab resistance before and after the COVID-19 pandemic. However, RSV-specific drug-resistance substitutions for suptavumab were identified.

背景:呼吸道合胞病毒(RSV)是一种传播性极强的病毒,是下呼吸道感染的主要病因。我们研究了韩国 2019 年冠状病毒病(COVID-19)大流行前后 RSV 基因组的分子变化,并调查了是否存在耐药突变:在这项前瞻性单中心研究中,在 2019 年 9 月至 2022 年 12 月期间收集了 RSV 阳性的呼吸道样本。进行了长线程全基因组测序(WGS),并调查了帕利珠单抗、尼尔赛维单抗和苏帕珠单抗是否存在已知的耐药替代:共收集了 276 名儿童的 288 份呼吸道样本。有 133 份样本(分别有 71 份和 62 份样本来自流行前和流行后)的 WGS 数据。所有 RSV-A 株系(n = 56)都属于 GA2.3.5 (ON1) 基因型,而所有 RSV-B 株系(n = 77)都属于 GB5.0.5a (BA) 基因型。在疫情流行前和疫情流行后,基因型没有明显差异。此外,在 F 基因中未发现与尼舍单抗或帕利珠单抗耐药性有关的明显突变。然而,在所有RSV-B样本中都出现了L172Q和S173L取代,而已知这两种取代可使患者对索帕珠单抗产生耐药性:结论:尽管RSV的季节性出现了前所未有的中断,但在COVID-19大流行前后,韩国循环中的RSV菌株与尼舍维单抗或帕利珠单抗耐药性有关的分子变化并不明显。不过,发现了RSV特异性耐药替代物苏妥珠单抗。
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引用次数: 0
What to Know Before Prescribing Antidepressants to Depressed Youths: A Focus on the Black Box Warning. 为抑郁青少年开具抗抑郁药处方前的注意事项:关注黑框警告。
IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-07-15 DOI: 10.3346/jkms.2024.39.e212
Minha Hong
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引用次数: 0
In This Issue on 15-July-2024. 本期日期:2024 年 7 月 15 日。
IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-07-15 DOI: 10.3346/jkms.2024.39.e213
Jin-Hong Yoo
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引用次数: 0
Validation of the Utility of the Genetically Shared Regions of Chromosomes (GD-ICS) Measuring Method in Identifying Complicated Genetic Relatedness. 验证染色体基因共享区(GD-ICS)测量方法在确定复杂遗传相关性中的实用性。
IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-07-15 DOI: 10.3346/jkms.2024.39.e198
Sohee Cho, Eunsoon Shin, YoonGi Park, Haeun You, Eun Young Lee, Jong-Eun Lee, Soong Deok Lee

Background: Relatives share more genomic regions than unrelated individuals, with closer relatives sharing more regions. This concept, paired with the increased availability of high-throughput single nucleotide polymorphism (SNP) genotyping technologies, has made it feasible to measure the shared chromosomal regions between individuals to assess their level of relation to each other. However, such techniques have remained in the conceptual rather than practical stages in terms of applying measures or indices. Recently, we developed an index called "genetic distance-based index of chromosomal sharing (GD-ICS)" utilizing large-scale SNP data from Korean family samples and demonstrated its potential for practical applications in kinship determination. In the current study, we present validation results from various real cases demonstrating the utility of this method in resolving complex familial relationships where information obtained from traditional short tandem repeats (STRs) or lineage markers is inconclusive.

Methods: We obtained large-scale SNP data through microarray analysis from Korean individuals involving 13 kinship cases and calculated GD-ICS values using the method described in our previous study. Based on the GD-ICS reference constructed for Korean families, each disputed kinship was evaluated and validated using a combination of traditional STRs and lineage markers.

Results: The cases comprised those A) that were found to be inconclusive using the traditional approach, B) for which it was difficult to apply traditional testing methods, and C) that were more conclusively resolved using the GD-ICS method. This method has overcome the limitations faced by traditional STRs in kinship testing, particularly in a paternity case with STR mutational events and in confirming distant kinship where the individual of interest is unavailable for testing. It has also been demonstrated to be effective in identifying various relationships without specific presumptions and in confirming a lack of genetic relatedness between individuals.

Conclusion: This method has been proven effective in identifying familial relationships across diverse complex and practical scenarios. It is not only useful when traditional testing methods fail to provide conclusive results, but it also enhances the resolution of challenging kinship cases, which suggests its applicability in various types of practical casework.

背景亲属比非亲属共享更多的基因组区域,近亲共享的区域更多。这一概念,再加上高通量单核苷酸多态性(SNP)基因分型技术的日益普及,使得测量个体之间共享的染色体区域以评估他们之间的关系变得可行。然而,此类技术在应用措施或指数方面仍停留在概念阶段,而非实践阶段。最近,我们利用来自韩国家族样本的大规模 SNP 数据开发了一种名为 "基于遗传距离的染色体共享指数(GD-ICS)"的指数,并证明了其在亲缘关系测定中的实际应用潜力。在本研究中,我们展示了各种实际案例的验证结果,证明了这种方法在解决复杂的家族关系问题上的实用性,因为在这些问题上,从传统的短串联重复序列(STR)或世系标记中获得的信息是不确定的:方法:我们通过微阵列分析获得了韩国人的大规模 SNP 数据,涉及 13 个亲缘关系病例,并使用之前研究中描述的方法计算了 GD-ICS 值。根据为韩国家族构建的 GD-ICS 参考值,使用传统 STR 和世系标记对每个有争议的亲属关系进行了评估和验证:这些案例包括:A) 使用传统方法无法得出结论的案例;B) 难以使用传统检测方法的案例;C) 使用 GD-ICS 方法能更明确地解决问题的案例。这种方法克服了传统 STR 在亲缘关系检测中面临的局限性,尤其是在有 STR 变异事件的亲子鉴定案例中,以及在相关个体无法接受检测的情况下确认远亲关系时。此外,该方法还被证明能有效识别各种关系,而无需特定的推断,并能确认个体之间缺乏遗传亲缘关系:结论:这种方法已被证明能在各种复杂和实际的情况下有效识别家族关系。它不仅在传统检测方法无法提供结论性结果时有用,而且还能提高解决具有挑战性的亲属关系案件的能力,这表明它适用于各种类型的实际个案工作。
{"title":"Validation of the Utility of the Genetically Shared Regions of Chromosomes (GD-ICS) Measuring Method in Identifying Complicated Genetic Relatedness.","authors":"Sohee Cho, Eunsoon Shin, YoonGi Park, Haeun You, Eun Young Lee, Jong-Eun Lee, Soong Deok Lee","doi":"10.3346/jkms.2024.39.e198","DOIUrl":"10.3346/jkms.2024.39.e198","url":null,"abstract":"<p><strong>Background: </strong>Relatives share more genomic regions than unrelated individuals, with closer relatives sharing more regions. This concept, paired with the increased availability of high-throughput single nucleotide polymorphism (SNP) genotyping technologies, has made it feasible to measure the shared chromosomal regions between individuals to assess their level of relation to each other. However, such techniques have remained in the conceptual rather than practical stages in terms of applying measures or indices. Recently, we developed an index called \"genetic distance-based index of chromosomal sharing (GD-ICS)\" utilizing large-scale SNP data from Korean family samples and demonstrated its potential for practical applications in kinship determination. In the current study, we present validation results from various real cases demonstrating the utility of this method in resolving complex familial relationships where information obtained from traditional short tandem repeats (STRs) or lineage markers is inconclusive.</p><p><strong>Methods: </strong>We obtained large-scale SNP data through microarray analysis from Korean individuals involving 13 kinship cases and calculated GD-ICS values using the method described in our previous study. Based on the GD-ICS reference constructed for Korean families, each disputed kinship was evaluated and validated using a combination of traditional STRs and lineage markers.</p><p><strong>Results: </strong>The cases comprised those A) that were found to be inconclusive using the traditional approach, B) for which it was difficult to apply traditional testing methods, and C) that were more conclusively resolved using the GD-ICS method. This method has overcome the limitations faced by traditional STRs in kinship testing, particularly in a paternity case with STR mutational events and in confirming distant kinship where the individual of interest is unavailable for testing. It has also been demonstrated to be effective in identifying various relationships without specific presumptions and in confirming a lack of genetic relatedness between individuals.</p><p><strong>Conclusion: </strong>This method has been proven effective in identifying familial relationships across diverse complex and practical scenarios. It is not only useful when traditional testing methods fail to provide conclusive results, but it also enhances the resolution of challenging kinship cases, which suggests its applicability in various types of practical casework.</p>","PeriodicalId":16249,"journal":{"name":"Journal of Korean Medical Science","volume":null,"pages":null},"PeriodicalIF":3.0,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11249576/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141626929","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Current Incidence and Future Projection of Acetabular Fractures in Korea. 韩国髋臼骨折的当前发病率和未来预测。
IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-07-15 DOI: 10.3346/jkms.2024.39.e204
Ki-Tae Park, Eun Kyung Park, Dong-Hoon Lee, Joon Hwan An, Jonghwa Won, Sung Hwa Kim, Young-Kyun Lee, Jung-Wee Park

Background: As one of the most challenging fractures to orthopedic surgeons, acetabular fractures show a wide range of incidence among countries and regions with even more variance in the treatment modalities. In this study, we aimed to investigate the epidemiology of acetabular fractures, and to compare the rate of subsequent total hip arthroplasty (THA) between nonoperative and operative treatments in South Korea using a medical claims database.

Methods: This was a retrospective study using the Korean Health Insurance Review and Assessment database. Patients admitted for acetabular fractures from January 2007 to December 2018 were identified using International Classification of Diseases-10 codes. Kaplan-Meier survival analysis was used to compare the cumulative incidence of THA between two groups. We also evaluated the survivorship of operative group according to the type of institutions.

Results: The incidence rate of acetabular fractures increased by 28% between 2007 and 2018. Acetabular fractures were more common in men (62%) than women (38%), and most common in the patients older than 80 years. The number of acetabular fractures was estimated to increase 1.7-fold in 2030 compared to 2018. Operative treatment accounted for 16% of cases, and nonoperative treatment for 84%. The incidence of subsequent THA was higher in the operative treatment group than in the nonoperative group (P < 0.001). The higher rate in the operative treatment group is probably related with the severity of the fracture type. The rate of subsequent THA was higher in patients who initially treated in general hospitals compared with those who were initially treated in tertiary hospitals.

Conclusion: The incidence of acetabular fractures is increasing in South Korea, in line with global trends. Most acetabular fractures are treated conservatively, and those who receive surgery are more likely to require a subsequent THA. Patients who were operated in general hospitals had highest possibility of subsequent THA after acetabular fractures.

背景:髋臼骨折是骨科医生面临的最具挑战性的骨折之一,在不同国家和地区的发病率差异很大,治疗方法的差异更大。在这项研究中,我们旨在调查髋臼骨折的流行病学,并利用医疗索赔数据库比较韩国非手术治疗和手术治疗的后续全髋关节置换术(THA)的比例:这是一项利用韩国健康保险审查和评估数据库进行的回顾性研究。2007年1月至2018年12月期间因髋臼骨折入院的患者均使用《国际疾病分类-10》代码进行识别。采用 Kaplan-Meier 生存分析比较两组患者的 THA 累计发生率。我们还根据机构类型评估了手术组的存活率:2007年至2018年间,髋臼骨折的发生率增加了28%。髋臼骨折的男性发病率(62%)高于女性(38%),在80岁以上的患者中最为常见。据估计,与2018年相比,2030年髋臼骨折的数量将增加1.7倍。手术治疗占16%,非手术治疗占84%。手术治疗组的后续 THA 发生率高于非手术治疗组(P < 0.001)。手术治疗组的发病率较高可能与骨折类型的严重程度有关。与在三甲医院接受治疗的患者相比,最初在综合医院接受治疗的患者随后接受 THA 的比例更高:结论:髋臼骨折的发病率在韩国呈上升趋势,这与全球趋势一致。大多数髋臼骨折患者都接受了保守治疗,而接受手术治疗的患者更有可能需要接受后续的THA治疗。在综合医院接受手术的患者在髋臼骨折后进行后续THA的可能性最高。
{"title":"The Current Incidence and Future Projection of Acetabular Fractures in Korea.","authors":"Ki-Tae Park, Eun Kyung Park, Dong-Hoon Lee, Joon Hwan An, Jonghwa Won, Sung Hwa Kim, Young-Kyun Lee, Jung-Wee Park","doi":"10.3346/jkms.2024.39.e204","DOIUrl":"10.3346/jkms.2024.39.e204","url":null,"abstract":"<p><strong>Background: </strong>As one of the most challenging fractures to orthopedic surgeons, acetabular fractures show a wide range of incidence among countries and regions with even more variance in the treatment modalities. In this study, we aimed to investigate the epidemiology of acetabular fractures, and to compare the rate of subsequent total hip arthroplasty (THA) between nonoperative and operative treatments in South Korea using a medical claims database.</p><p><strong>Methods: </strong>This was a retrospective study using the Korean Health Insurance Review and Assessment database. Patients admitted for acetabular fractures from January 2007 to December 2018 were identified using International Classification of Diseases-10 codes. Kaplan-Meier survival analysis was used to compare the cumulative incidence of THA between two groups. We also evaluated the survivorship of operative group according to the type of institutions.</p><p><strong>Results: </strong>The incidence rate of acetabular fractures increased by 28% between 2007 and 2018. Acetabular fractures were more common in men (62%) than women (38%), and most common in the patients older than 80 years. The number of acetabular fractures was estimated to increase 1.7-fold in 2030 compared to 2018. Operative treatment accounted for 16% of cases, and nonoperative treatment for 84%. The incidence of subsequent THA was higher in the operative treatment group than in the nonoperative group (<i>P</i> < 0.001). The higher rate in the operative treatment group is probably related with the severity of the fracture type. The rate of subsequent THA was higher in patients who initially treated in general hospitals compared with those who were initially treated in tertiary hospitals.</p><p><strong>Conclusion: </strong>The incidence of acetabular fractures is increasing in South Korea, in line with global trends. Most acetabular fractures are treated conservatively, and those who receive surgery are more likely to require a subsequent THA. Patients who were operated in general hospitals had highest possibility of subsequent THA after acetabular fractures.</p>","PeriodicalId":16249,"journal":{"name":"Journal of Korean Medical Science","volume":null,"pages":null},"PeriodicalIF":3.0,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11249580/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141626927","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Trends and Barriers in Diabetic Retinopathy Screening: Korea National Health and Nutritional Examination Survey 2016-2021. 糖尿病视网膜病变筛查的趋势与障碍:2016-2021年韩国国民健康与营养调查》。
IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-07-15 DOI: 10.3346/jkms.2024.39.e203
Min Seok Kim, Sang Jun Park, Kwangsic Joo, Se Joon Woo

Background: The prevalence of diabetes is increasing globally, highlighting the importance of preventive healthcare. This study aimed to identify the diabetic retinopathy (DR) screening rates and risk factors linked to DR screening nonadherence in the Korean population through a nationally representative sample survey.

Methods: Among the Korea National Health and Nutrition Examination Survey database from 2016 to 2021, participants aged ≥ 40 years with diabetes were included. The weighted estimate for nonadherence to DR screening within a year was calculated. Risk factor analyses were conducted using univariate and multivariate logistic regression.

Results: Among the 3,717 participants, 1,109 (29.5%) underwent DR screening within the past year, and this national estimate exhibited no statistically significant difference from 2016 to 2021 (P = 0.809). Nonadherence to annual DR screening was associated with residing in rural areas, age ≥ 80 years, low educational level, self-reported good health, absence of ocular disease, current smoking, lack of exercise and dietary diabetes treatment, and no activity limitation (all P < 0.05).

Conclusion: The recent DR screening rate in Korea was relatively low. Factors associated with apathy and complacency towards personal health were associated with the nonadherence to DR screening. Educational interventions have the potential to enhance the annual screening rate for diabetic patients.

背景:在全球范围内,糖尿病的发病率不断上升,这凸显了预防性保健的重要性。本研究旨在通过一项具有全国代表性的抽样调查,确定韩国人口中糖尿病视网膜病变(DR)筛查率以及与不坚持DR筛查相关的风险因素:在 2016 年至 2021 年韩国国民健康与营养调查数据库中,纳入了年龄≥ 40 岁的糖尿病患者。计算一年内未坚持DR筛查的加权估计值。使用单变量和多变量逻辑回归进行了风险因素分析:在 3,717 名参与者中,1,109 人(29.5%)在过去一年内接受了 DR 筛查,这一全国性估计值与 2016 年至 2021 年相比无显著统计学差异(P = 0.809)。不坚持每年进行DR筛查与以下因素有关:居住在农村地区、年龄≥80岁、受教育程度低、自称健康状况良好、没有眼部疾病、目前吸烟、缺乏运动和饮食治疗糖尿病以及没有活动限制(所有P均<0.05):结论:韩国近期的 DR 筛查率相对较低。结论:韩国近期的 DR 筛查率相对较低,对个人健康的冷漠和自满与不坚持 DR 筛查有关。教育干预措施有可能提高糖尿病患者的年度筛查率。
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引用次数: 0
Machine Learning-Based Identification of Diagnostic Biomarkers for Korean Male Sarcopenia Through Integrative DNA Methylation and Methylation Risk Score: From the Korean Genomic Epidemiology Study (KoGES). 通过整合 DNA 甲基化和甲基化风险评分,基于机器学习识别韩国男性 "肌肉疏松症 "诊断生物标志物:韩国基因组流行病学研究》(KoGES)。
IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-07-08 DOI: 10.3346/jkms.2024.39.e200
Seohyun Ahn, Yunho Sung, Wook Song

Background: Sarcopenia, characterized by a progressive decline in muscle mass, strength, and function, is primarily attributable to aging. DNA methylation, influenced by both genetic predispositions and environmental exposures, plays a significant role in sarcopenia occurrence. This study employed machine learning (ML) methods to identify differentially methylated probes (DMPs) capable of diagnosing sarcopenia in middle-aged individuals. We also investigated the relationship between muscle strength, muscle mass, age, and sarcopenia risk as reflected in methylation profiles.

Methods: Data from 509 male participants in the urban cohort of the Korean Genome Epidemiology Study_Health Examinee study were categorized into quartile groups based on the sarcopenia criteria for appendicular skeletal muscle index (ASMI) and handgrip strength (HG). To identify diagnostic biomarkers for sarcopenia, we used recursive feature elimination with cross validation (RFECV), to pinpoint DMPs significantly associated with sarcopenia. An ensemble model, leveraging majority voting, was utilized for evaluation. Furthermore, a methylation risk score (MRS) was calculated, and its correlation with muscle strength, function, and age was assessed using likelihood ratio analysis and multinomial logistic regression.

Results: Participants were classified into two groups based on quartile thresholds: sarcopenia (n = 37) with ASMI and HG in the lowest quartile, and normal ranges (n = 48) in the highest. In total, 238 DMPs were identified and eight probes were selected using RFECV. These DMPs were used to build an ensemble model with robust diagnostic capabilities for sarcopenia, as evidenced by an area under the receiver operating characteristic curve of 0.94. Based on eight probes, the MRS was calculated and then validated by analyzing age, HG, and ASMI among the control group (n = 424). Age was positively correlated with high MRS (coefficient, 1.2494; odds ratio [OR], 3.4882), whereas ASMI and HG were negatively correlated with high MRS (ASMI coefficient, -0.4275; OR, 0.6521; HG coefficient, -0.3116; OR, 0.7323).

Conclusion: Overall, this study identified key epigenetic markers of sarcopenia in Korean males and developed a ML model with high diagnostic accuracy for sarcopenia. The MRS also revealed significant correlations between these markers and age, HG, and ASMI. These findings suggest that both diagnostic models and the MRS can play an important role in managing sarcopenia in middle-aged populations.

背景:肌肉疏松症的特点是肌肉质量、力量和功能逐渐下降,主要归因于衰老。DNA 甲基化受遗传倾向和环境暴露的影响,在肌肉疏松症的发生中起着重要作用。本研究采用机器学习(ML)方法来识别能够诊断中年人肌肉疏松症的差异甲基化探针(DMPs)。我们还研究了甲基化图谱所反映的肌肉力量、肌肉质量、年龄与肌肉疏松症风险之间的关系:根据肌肉疏松症标准中的骨骼肌指数(ASMI)和手握力(HG),我们将韩国基因组流行病学研究_健康体检者研究城市队列中 509 名男性参与者的数据分为四分位组。为了确定肌肉疏松症的诊断生物标志物,我们使用了交叉验证递归特征消除法(RFECV),以确定与肌肉疏松症显著相关的DMPs。在评估时,我们使用了一个利用多数投票的集合模型。此外,还计算了甲基化风险评分(MRS),并使用似然比分析和多项式逻辑回归评估了其与肌肉力量、功能和年龄的相关性:根据四分位数阈值将参与者分为两组:最低四分位数为患有 ASMI 和 HG 的肌少症(37 人),最高四分位数为正常范围(48 人)。总共确定了 238 个 DMP,并使用 RFECV 选择了 8 个探针。这些 DMPs 被用来建立一个具有强大肌少症诊断能力的集合模型,接收者操作特征曲线下面积为 0.94。根据八个探针计算出 MRS,然后通过分析对照组(n = 424)的年龄、HG 和 ASMI 进行验证。年龄与高MRS呈正相关(系数,1.2494;比值比[OR],3.4882),而ASMI和HG与高MRS呈负相关(ASMI系数,-0.4275;比值比,0.6521;HG系数,-0.3116;比值比,0.7323):总之,本研究确定了韩国男性肌肉疏松症的关键表观遗传标记,并建立了一个具有较高诊断准确性的肌肉疏松症 ML 模型。MRS 还揭示了这些标记物与年龄、HG 和 ASMI 之间的显著相关性。这些研究结果表明,诊断模型和磁共振成像可在中年人群肌肉疏松症的管理中发挥重要作用。
{"title":"Machine Learning-Based Identification of Diagnostic Biomarkers for Korean Male Sarcopenia Through Integrative DNA Methylation and Methylation Risk Score: From the Korean Genomic Epidemiology Study (KoGES).","authors":"Seohyun Ahn, Yunho Sung, Wook Song","doi":"10.3346/jkms.2024.39.e200","DOIUrl":"10.3346/jkms.2024.39.e200","url":null,"abstract":"<p><strong>Background: </strong>Sarcopenia, characterized by a progressive decline in muscle mass, strength, and function, is primarily attributable to aging. DNA methylation, influenced by both genetic predispositions and environmental exposures, plays a significant role in sarcopenia occurrence. This study employed machine learning (ML) methods to identify differentially methylated probes (DMPs) capable of diagnosing sarcopenia in middle-aged individuals. We also investigated the relationship between muscle strength, muscle mass, age, and sarcopenia risk as reflected in methylation profiles.</p><p><strong>Methods: </strong>Data from 509 male participants in the urban cohort of the Korean Genome Epidemiology Study_Health Examinee study were categorized into quartile groups based on the sarcopenia criteria for appendicular skeletal muscle index (ASMI) and handgrip strength (HG). To identify diagnostic biomarkers for sarcopenia, we used recursive feature elimination with cross validation (RFECV), to pinpoint DMPs significantly associated with sarcopenia. An ensemble model, leveraging majority voting, was utilized for evaluation. Furthermore, a methylation risk score (MRS) was calculated, and its correlation with muscle strength, function, and age was assessed using likelihood ratio analysis and multinomial logistic regression.</p><p><strong>Results: </strong>Participants were classified into two groups based on quartile thresholds: sarcopenia (n = 37) with ASMI and HG in the lowest quartile, and normal ranges (n = 48) in the highest. In total, 238 DMPs were identified and eight probes were selected using RFECV. These DMPs were used to build an ensemble model with robust diagnostic capabilities for sarcopenia, as evidenced by an area under the receiver operating characteristic curve of 0.94. Based on eight probes, the MRS was calculated and then validated by analyzing age, HG, and ASMI among the control group (n = 424). Age was positively correlated with high MRS (coefficient, 1.2494; odds ratio [OR], 3.4882), whereas ASMI and HG were negatively correlated with high MRS (ASMI coefficient, -0.4275; OR, 0.6521; HG coefficient, -0.3116; OR, 0.7323).</p><p><strong>Conclusion: </strong>Overall, this study identified key epigenetic markers of sarcopenia in Korean males and developed a ML model with high diagnostic accuracy for sarcopenia. The MRS also revealed significant correlations between these markers and age, HG, and ASMI. These findings suggest that both diagnostic models and the MRS can play an important role in managing sarcopenia in middle-aged populations.</p>","PeriodicalId":16249,"journal":{"name":"Journal of Korean Medical Science","volume":null,"pages":null},"PeriodicalIF":3.0,"publicationDate":"2024-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11231442/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141558895","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Causality Assessment Framework for COVID-19 Vaccines and Adverse Events at the COVID-19 Vaccine Safety Research Center. COVID-19 疫苗和 COVID-19 疫苗安全研究中心不良事件的因果关系评估框架。
IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-07-08 DOI: 10.3346/jkms.2024.39.e220
Seyoung Kim, Jeong Ah Kim, Hyesook Park, Sohee Park, Sanghoon Oh, Seung Eun Jung, Hyoung-Shik Shin, Jong Koo Lee, Hee Chul Han, Jun Hee Woo, Byung-Joo Park, Nam-Kyong Choi, Dong-Hyun Kim

During the coronavirus disease 2019 (COVID-19) pandemic, conclusively evaluating possible associations between COVID-19 vaccines and potential adverse events was of critical importance. The National Academy of Medicine of Korea established the COVID-19 Vaccine Safety Research Center (CoVaSC) with support from the Korea Disease Control and Prevention Agency to investigate the scientific relationship between COVID-19 vaccines and suspected adverse events. Although determining whether the COVID-19 vaccine was responsible for any suspected adverse event necessitated a systematic approach, traditional causal inference theories, such as Hill's criteria, encountered certain limitations and criticisms. To facilitate a systematic and evidence-based evaluation, the United States Institute of Medicine, at the request of the Centers for Disease Control and Prevention, offered a detailed causality assessment framework in 2012, which was updated in the recent report by the National Academies of Sciences, Engineering, and Medicine (NASEM) in 2024. This framework, based on a weight-of-evidence approach, allows the independent evaluation of both epidemiological and mechanistic evidence, culminating in a comprehensive conclusion about causality. Epidemiological evidence derived from population studies is categorized into four levels-high, moderate, limited, or insufficient-while mechanistic evidence, primarily from biological and clinical studies in animals and individuals, is classified as strong, intermediate, weak, or lacking. The committee then synthesizes these two types of evidence to draw a conclusion about the causal relationship, which can be described as "convincingly supports" ("evidence established" in the 2024 NASEM report), "favors acceptance," "favors rejection," or "inadequate to accept or reject." The CoVaSC has established an independent committee to conduct causality assessments using the weight-of-evidence framework, specifically for evaluating the causality of adverse events associated with COVID-19 vaccines. The aim of this study is to provide an overview of the weight-of-evidence framework and to detail the considerations involved in its practical application in the CoVaSC.

在冠状病毒病 2019(COVID-19)大流行期间,对 COVID-19 疫苗与潜在不良事件之间可能存在的关联进行确证评估至关重要。韩国国家医学研究院在韩国疾病预防控制局的支持下成立了 COVID-19 疫苗安全研究中心(CoVaSC),以调查 COVID-19 疫苗与可疑不良事件之间的科学关系。尽管确定 COVID-19 疫苗是否对任何疑似不良事件负责需要采用系统的方法,但希尔标准等传统的因果推断理论存在一定的局限性和诟病。为便于进行系统的循证评估,美国医学研究所应美国疾病控制和预防中心的要求,于 2012 年提出了一个详细的因果关系评估框架,美国国家科学、工程和医学研究院(NASEM)在 2024 年的最新报告中对该框架进行了更新。该框架以证据权重法为基础,可对流行病学证据和机理证据进行独立评估,最终得出关于因果关系的综合结论。来自人群研究的流行病学证据分为四个等级--高、中、有限或不足,而机理证据主要来自动物和个体的生物和临床研究,分为强、中、弱或缺乏。然后,委员会综合这两类证据,得出关于因果关系的结论,该结论可被描述为 "令人信服地支持"(2024 年 NASEM 报告中的 "证据确凿")、"赞成接受"、"赞成拒绝 "或 "不足以接受或拒绝"。CoVaSC 成立了一个独立委员会,利用证据权重框架进行因果关系评估,专门用于评估 COVID-19 疫苗相关不良事件的因果关系。本研究旨在概述证据权重框架,并详细介绍该框架在 CoVaSC 实际应用中的注意事项。
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引用次数: 0
Relationship Between Aspirin Use and Site-Specific Colorectal Cancer Risk Among Individuals With Metabolic Comorbidity. 代谢性合并症患者服用阿司匹林与特定部位结直肠癌风险之间的关系。
IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-07-08 DOI: 10.3346/jkms.2024.39.e199
Seokyung An, Madhawa Gunathilake, Jeonghee Lee, Minji Kim, Jae Hwan Oh, Hee Jin Chang, Dae Kyung Sohn, Aesun Shin, Jeongseon Kim

Background: The relationship between aspirin usage and the risk of colorectal cancer (CRC) among individuals with both hypertension (HTN) and diabetes mellitus (DM) remains unclear. This study aims to explore the impact of aspirin use on the site-specific CRC risk in patients with metabolic comorbidity.

Methods: A case-control study was conducted among 1,331 CRC patients and 2,771 controls recruited from the Nation Cancer Center in Korea. Multinomial logistic regression analyses were used to calculate the odds ratios (ORs) and 95% confidence intervals (CIs) for the association between aspirin use, metabolic disease status, and site-specific CRC risk.

Results: Among the 4,102 participants, 1,191 individuals had neither HTN nor DM, 2,044 were diagnosed with HTN, 203 with DM, and 664 presented with HTN and DM comorbidity. An increasing number of HTN and DM was associated with an increased risk of overall CRC (HTN or DM: OR, 1.70; 95% CI, 1.39-2.07; HTN and DM: OR, 8.43; 95% CI, 6.37-11.16), while aspirin use was associated with a decreased risk of overall CRC (OR, 0.31; 95% CI, 0.21-0.46). These results remained consistent across anatomical sites. Among individuals with HTN and DM comorbidity, aspirin use notably associated with lower risk of overall CRC (OR, 0.39; 95% CI, 0.21-0.72), proximal colon (OR, 0.32; 95% CI, 0.13-0.71) and rectal cancer (OR, 0.27; 95% CI, 0.08-0.97), but not distal colon cancer (OR, 0.58; 95% CI, 0.27-1.24).

Conclusion: This study showed that aspirin use is negatively associated with overall and site-specific CRC, even among individuals with HTN and DM comorbidity.

背景:高血压(HTN)和糖尿病(DM)患者服用阿司匹林与结直肠癌(CRC)风险之间的关系仍不清楚。本研究旨在探讨阿司匹林的使用对代谢合并症患者特定部位 CRC 风险的影响:方法:对从韩国国立癌症中心招募的 1,331 名 CRC 患者和 2,771 名对照者进行了病例对照研究。结果:在 4102 名参与者中,1,331 人使用阿司匹林,而 2,771 人未使用阿司匹林:在 4102 名参与者中,1191 人既无高血压也无糖尿病,2044 人被诊断为高血压,203 人被诊断为糖尿病,664 人合并高血压和糖尿病。高血压和糖尿病患者人数的增加与总的 CRC 风险增加有关(高血压或糖尿病:OR,1.70;95% CI,1.39-2.07;高血压和糖尿病:OR,8.43;95% CI,6.37-11.16),而服用阿司匹林与总的 CRC 风险降低有关(OR,0.31;95% CI,0.21-0.46)。这些结果在不同的解剖部位保持一致。在合并高血压和糖尿病的人群中,服用阿司匹林明显与总体 CRC(OR,0.39;95% CI,0.21-0.72)、近端结肠癌(OR,0.32;95% CI,0.13-0.71)和直肠癌(OR,0.27;95% CI,0.08-0.97)的风险降低有关,但与远端结肠癌(OR,0.58;95% CI,0.27-1.24)的风险降低无关:本研究表明,即使是合并高血压和糖尿病的人,服用阿司匹林与总体和部位特异性结肠癌也呈负相关。
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引用次数: 0
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Journal of Korean Medical Science
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