Upsala Journal of Medical Sciences https://ujms.net/index.php/ujms <p>Indexed in the Science Citation Index and MEDLINE, this open access journal welcomes both clinical and experimental contributions from across the entire medical field. It is read by an international audience,&nbsp;has no publishing charges and makes short decision times a high priority.</p> Upsala Medical Society en-US Upsala Journal of Medical Sciences 0300-9734 <p>Authors retain copyright of their work, with first publication rights granted to Upsala Medical Society. Read the full <a href="https://ujms.net/index.php/ujms/oapolicy">Copyright- and Licensing Statement</a>.</p> A Japanese translation of the Swedish Universities Scales of Personality https://ujms.net/index.php/ujms/article/view/10349 <p><strong>Background</strong>: The Swedish Universities Scales of Personality (SSP) is a personality measurement tool with a short test battery of high psychometric quality, previously not availiable in Japanese.</p> <p><strong>Methods</strong>: We translated the SSP into Japanese and administered it to 103 Japanese nationals. For 11 of the 13 SSP scales in the Japanese version of the SSP (SSP-J11), the Cronbach’s alpha ranged from 0.50 to 0.82 with good internal scale reliability.</p> <p><strong>Results</strong>: A principal factor analysis replicated the previous work by identifying the same three principal dimensions of Neuroticism, Aggression, and Extraversion factors.</p> <p><strong>Conclusion</strong>: The resulting three-factor SSP-J11 shows acceptable reliability and should provide informative insights about personality traits in research and clinical practice in a Japanese context.</p> Lykke Silfwerbrand Lisa Ekselius Yasuharu Koike Malin Gingnell Copyright (c) 2024 Lykke Silfwerbrand, Lisa Ekselius, Yasuharu Koike, Malin Gingnell https://creativecommons.org/licenses/by/4.0 2024-03-21 2024-03-21 129 e10349 e10349 10.48101/ujms.v129.10349 Expression of HIF-α and their association with clinicopathological parameters in clinical renal cell carcinoma https://ujms.net/index.php/ujms/article/view/9407 <p><strong>Objectives</strong>: This study aimed to assess the cellular localization and expression levels of hypoxia-inducible factor (HIF) -α proteins (specifically HIF-1α, HIF-2α, and HIF-3α) that play a role in the hypoxia pathway and to determine their correlation with clinicopathological parameters and patient survival in renal cell carcinoma (RCC).</p> <p><strong>Materials and methods</strong>: Tissue microarray (TMA) with cores from 150 clear cell RCCs and 31 non-ccRCC samples. HIF-1α, HIF-2α, and HIF-3α antibodies were used for immunohistochemistry (IHC) of TMA to evaluate the cellular localization and expression levels of HIF-α proteins, specifically in relation to the hypoxia pathway.</p> <p><strong>Results</strong>: The expression levels of the HIF-α proteins were higher in the nucleus than in the cytoplasm. Furthermore, the nuclear expression levels of all HIF-α proteins were significantly higher in clear cell RCC (ccRCC) than in non-ccRCC. Cytoplasmic HIF-3α expression was also higher in ccRCC than in non-ccRCC, whereas cytoplasmic HIF-1α and HIF-2α expression levels were similar between the different RCC types. In ccRCC, nuclear HIF-1α expression levels correlated with both nuclear HIF-2α and HIF-3α levels, whereas cytoplasmic HIF-3α expression levels were associated with HIF-1α only.</p> <p>In non-ccRCC, there was a positive correlation observed between nuclear HIF-1α and HIF-3α expression, but no correlation was found with HIF-2α. In patients with ccRCC, the nuclear expressions of HIF-1α and HIF-3α was significantly associated with cancer-specific survival (CSS) in univariate analysis. This association was no longer evident in multivariate analysis. Notably, there was no correlation observed between nuclear HIF-2α expression and CSS in these patients. In contrast, cytoplasmic expression levels showed no association with CSS.</p> <p><strong>Conclusion</strong>: The expression levels of the three primary HIF-α proteins were found to be higher in the nucleus than in the cytoplasm. Furthermore, the results indicated that HIF-3α and HIF-1α expression levels were significant univariate factors associated with CSS in patients with clear cell RCC. These results highlight the critical role that HIF-3α and HIF-1α play in the hypoxia pathway.</p> Raviprakash T. Sitaram Börje Ljungberg Copyright (c) 2024 Raviprakash T. Sitaram, Börje Ljungberg https://creativecommons.org/licenses/by/4.0 2024-03-21 2024-03-21 129 e9407 e9407 10.48101/ujms.v129.9407 Age and co-morbidities as independent risk factors of infections leading to hospital admission in the last year of life among the elderly: A retrospective registry-based study https://ujms.net/index.php/ujms/article/view/10504 <p><strong>Background</strong>: The immune system declines with age, but the impact of chronological age may be affected by sex, co-morbidities, and sociodemographic factors.</p> <p><strong>Objective</strong>: The article aims to study infections associated with hospital admission in the elderly in their last year of life and the impact of age, sex, co-morbidities, and sociodemographic factors.</p> <p><strong>Method</strong>: A retrospective study based on registry data covering all care visits in Stockholm Region, Sweden, for 7 years was conducted. All deceased subjects with at least one hospital admission with infection as the main diagnosis in the last year of life were compared with subjects with no such admission. Subjects were categorized into three different age-groups 65–79, 80–89, and 90 years and above. Co-morbidity was measured by the Charlson Comorbidity Index (CCI) and sociodemographic factors were assessed using the ‘Mosaic-system’. Subjects living in nursing homes were analyzed separately. Uni- and multivariable logistic regressions were conducted.</p> <p><strong>Results</strong>: Of the 55,238 subjects in the study population, 14,192 (26%) had at least one hospital admission due to infection in the last year of life. The risk of having a severe infection increased with age, adjusted odds ratio (OR): 1.30 (1.25–1.36), and 1.60 (1.52–1.69) for the age-groups 80–89 and ≥ 90 compared to the age-group 65–79. The most important factor for infection was a high co-morbidity score; adjusted OR: 1.75 (1.68–1.82). Male sex and living in a less affluent area were weaker risk factors for infections.</p> <p><strong>Conclusion</strong>: Chronological age and co-morbidities are independent risk factors of infections associated with hospital admission in the last year in life while male sex and sociodemographic factors have less impact.</p> Linda Björkhem-Bergman Torbjörn Schultz Peter Strang Copyright (c) 2024 Linda Björkhem-Bergman, Torbjörn Schultz, Peter Strang https://creativecommons.org/licenses/by/4.0 2024-03-13 2024-03-13 129 e10504 e10504 10.48101/ujms.v129.10504 The relationship between game genre, monetization strategy and symptoms of gaming disorder in a clinical sample of adolescents https://ujms.net/index.php/ujms/article/view/10386 <p><strong>Background</strong>: Gaming disorder (GD) has been introduced as a new diagnosis in the International Classification of Disease 11 (ICD-11). Currently, there’s limited understanding of how various video games may differentially contribute to the risk of developing GD. The main aim of this study was to examine the relationship between individuals’ game genre preferences, their preferred games’ monetization strategies, and GD Symptoms.</p> <p><strong>Methods</strong>: A total of 85 patients undergoing treatment for GD at a child and youth psychiatric clinic were included in the study. Their preferred games were classified into five novel genres based on gameplay similarities and objectives, and further categorized based on their monetization strategy.</p> <p><strong>Results</strong>: Symptom burden of GD, measured with Game Addiction Scale for Adolescents (GASA), was highest for those playing Free-to-Play (F2P) games and lowest for Pay-to-Play (P2P) players. Players of Competitive Games endorsed higher GD symptom burden, whereas players of Story-driven games reported lower GD symptom burden. Symptoms of GD were associated with attention-deficit hyperactivity disorder (ADHD) diagnosis in males.</p> <p><strong>Conclusions</strong>: This study reveals that game genre preference is influenced by sex, age, and certain psychiatric diagnoses. The categorizing of games into genres is increasingly complex and our research introduces a novel categorization in a developing research field. The result of this study suggests that the monetization model is important to consider while trying to understand the relationship between game characteristics and GD symptoms.</p> Frida André Per Bore Theo Toresson Mitchell Andersson Emma Claesdotter-Knutsson Copyright (c) 2024 Frida André, Per Bore, Theo Toresson, Mitchell Andersson, Emma Claesdotter-Knutsson https://creativecommons.org/licenses/by/4.0 2024-03-07 2024-03-07 129 e10386 e10386 10.48101/ujms.v129.10386 Partly unequal receipt of healthcare in last month of life in amyotrophic lateral sclerosis: a retrospective cohort study of the Stockholm region https://ujms.net/index.php/ujms/article/view/9856 <p><strong>Context</strong>: In amyotrophic lateral sclerosis (ALS), equal care is important, given that the disease often has complex symptoms at the end of life.</p> <p><strong>Objectives</strong>: The aim was to study the possible associations between demographic and clinical factors, including age, sex, and frailty, with acute healthcare utilization in the last month of life, measured by emergency room (ER) visits, admissions to acute hospitals and, acute hospitals as place of death, among patients with ALS. A second aim was to study whether receipt of specialized palliative care (SPC) affects above-mentioned healthcare utilization.</p> <p><strong>Methods</strong>: Observational, retrospective study based on Region Stockholm’s administrative data warehouse (VAL) in Sweden. Data were retrieved for 2015–2021 and analyzed with descriptive statistics and logistic regression models.</p> <p><strong>Results</strong>: All deceased patients (<em>n</em>&nbsp;= 448) ≥18 years with ALS were included. The mean age was 70.5 years, 46% were women and 58% had risk of frailty according to Hospital Frailty Risk Score (HFRS). Ninety-nine (22%) were nursing home residents and 49% received SPC. The receipt of SPC in patients with ALS was equal in relation to gender, socio-economic standing, frailty, and age &lt;75 years. Patients ≥75 years, those with dementia and/or residing in nursing homes (NH) were less likely to receive SPC (<em>P</em>&nbsp;= 0.01,&nbsp;<em>P</em>&nbsp;= 0.03 and&nbsp;<em>P</em>&nbsp;= 0.002, respectively). Receipt of SPC reduced ER visits (29% vs. 48%,&nbsp;<em>P</em>&nbsp;&lt; 0.001) and deaths at hospital (12% vs. 48%,&nbsp;<em>P</em>&nbsp;&lt;0.001). Patients who were frail, had a higher risk of ER visits and were more likely to die at an acute hospital setting (<em>P</em>&nbsp;&lt; 0.001 and&nbsp;<em>P</em>&nbsp;= 0.004). NH residents were less likely to have ER visits and to die in hospital (<em>P</em>&nbsp;= 0.002 and&nbsp;<em>P</em>&nbsp;= 0.005).</p> <p><strong>Conclusions</strong>: The results indicate partly unequal distribution of palliative care, however the actual, individual preferences cannot be deducted from registry studies. All patients with ALS should be offered SPC when needed.</p> <p><strong>Key message</strong>: This register study shows that receipt of SPC in patients with ALS is equal in relation to gender, socioeconomic standing, frailty, and age &lt;75 years, while those ≥75 years, with dementia, or residing in NH were somewhat less likely to receive SPC. Receipt of SPC reduces ER visits and acute hospital admissions.</p> Peter Strang Torbjörn Schultz Anneli Ozanne Copyright (c) 2024 Peter Strang, Torbjörn Schultz, Anneli Ozanne https://creativecommons.org/licenses/by/4.0 2024-02-08 2024-02-08 129 e9856 e9856 10.48101/ujms.v129.9856 A retrospective nationwide analysis of evolocumab use in Sweden and its effect on low-density lipoprotein cholesterol levels https://ujms.net/index.php/ujms/article/view/9618 <p><strong>Background</strong>: Treatment with proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors reduces low-density lipoprotein cholesterol (LDL-C) levels and decreases the incidence of major ischaemic events in clinical trials. However, less is known about the efficacy of PCSK9 inhibition in clinical practice. This study aimed to describe the change in LDL-C levels over time and LDL-C goal achievement in patients with/without atherosclerotic cardiovascular disease (ASCVD), who were prescribed evolocumab in clinical practice, and to describe adherence to and persistence with treatment.</p> <p><strong>Methods</strong>: Patients in Sweden with at least one evolocumab prescription filled between July 2015 and May 2020 were included. Medical history and lipid-lowering therapy (LLT) were sourced from national registries. LDL-C levels before and after treatment initiation were assessed using medical records. Persistence with and adherence to evolocumab and oral LLT were assessed up to 12 months after treatment initiation using the refill-gap method and proportion of days covered, respectively.</p> <p><strong>Results</strong>: Of the 2,360 patients with at least one prescription for evolocumab, 2,341 were included; 1,858 had ASCVD. Persistence with (76%) and adherence to (86%) evolocumab were high throughout the 12 months following initiation. Mean LDL-C levels decreased by 53% (95% confidence interval [CI]: 51–55%) in patients adherent to evolocumab (<em>n</em>&nbsp;= 567) and 59% (95% CI: 55–63%) in patients adherent to evolocumab and oral LLT (<em>n</em>&nbsp;= 186). Similar reductions in LDL-C were observed in patients with/without ASCVD. Reduced LDL-C levels remained stable during follow-up. Amongst patients adherent to evolocumab and those adherent to evolocumab and oral LLT, 23 and 55% achieved the LDL-C goal of &lt;1.4 mmol/L, respectively.</p> <p><strong>Conclusions</strong>: The evolocumab LDL-C-lowering effect observed in clinical trials was confirmed in clinical practice in Sweden, particularly in patients also treated with oral LLT. During follow-up, adherence to and persistence with evolocumab were high, with stable reduced levels of LDL-C during observation.</p> Maria K. Svensson Stefan James Annica Ravn-Fischer Guillermo Villa Lovisa Schalin Thomas Cars Stefan Gustafsson Emil Hagström Copyright (c) 2024 Maria K. Svensson, Stefan James, Annica Ravn-Fischer , Guillermo Villa, Lovisa Schalin , Thomas Cars, Stefan Gustafsson, Emil Hagström https://creativecommons.org/licenses/by/4.0 2024-02-01 2024-02-01 129 e9618 e9618 10.48101/ujms.v129.9618 COVID-19: Not a thrombotic disease but a thromboinflammatory disease https://ujms.net/index.php/ujms/article/view/9863 <p>While Coronavirus Disease in 2019 (COVID-19) may no longer be classified as a global public health emergency, it still poses a significant risk at least due to its association with thrombotic events. This study aims to reaffirm our previous hypothesis that COVID-19 is fundamentally a thrombotic disease. To accomplish this, we have undertaken an extensive literature review focused on assessing the comprehensive impact of COVID-19 on the entire hemostatic system. Our analysis revealed that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection significantly enhances the initiation of thrombin generation. However, it is noteworthy that the thrombin generation may be modulated by specific anticoagulants present in patients’ plasma. Consequently, higher levels of fibrinogen appear to play a more pivotal role in promoting coagulation in COVID-19, as opposed to thrombin generation. Furthermore, the viral infection can stimulate platelet activation either through widespread dissemination from the lungs to other organs or localized effects on platelets themselves. An imbalance between Von Willebrand Factor (VWF) and ADAMTS-13 also contributes to an exaggerated platelet response in this disease, in addition to elevated D-dimer levels, coupled with a significant increase in fibrin viscoelasticity. This paradoxical phenotype has been identified as ‘fibrinolysis shutdown’. To clarify the pathogenesis underlying these hemostatic disorders in COVID-19, we also examined published data, tracing the reaction process of relevant proteins and cells, from ACE2-dependent viral invasion, through induced tissue inflammation, endothelial injury, and innate immune responses, to occurrence of thrombotic events. We therefrom understand that COVID-19 should no longer be viewed as a thrombotic disease solely based on abnormalities in fibrin clot formation and proteolysis. Instead, it should be regarded as a thromboinflammatory disorder, incorporating both classical elements of cellular inflammation and their intricate interactions with the specific coagulopathy.</p> Shu He Margareta Blombäck Håkan Wallén Copyright (c) 2024 Shu He, Margareta Blombäck, Håkan Wallén https://creativecommons.org/licenses/by/4.0 2024-01-22 2024-01-22 129 e9863 e9863 10.48101/ujms.v129.9863