How SARS-CoV-2 infection affects acute ischemic stroke outcomes

United States News News

How SARS-CoV-2 infection affects acute ischemic stroke outcomes
United States Latest News,United States Headlines
  • 📰 NewsMedical
  • ⏱ Reading Time:
  • 62 sec. here
  • 3 min. at publisher
  • 📊 Quality Score:
  • News: 28%
  • Publisher: 71%

How SARS-CoV-2 infection affects acute ischemic stroke outcomes IschemicStroke SARSCoV2 Stroke Coronavirus Disease COVID Pneumonia Cardiovascular Reperfusion CreactiveProtein PLOSONE semmelweishu

By Dr. Priyom Bose, Ph.D.Mar 6 2023Reviewed by Danielle Ellis, B.Sc. The ongoing coronavirus disease 2019 pandemic, caused by severe acute respiratory syndrome coronavirus-2 , has affected millions of individuals worldwide, with a high rate of mortality and morbidity. Importantly, SARS-CoV-2 infection has been associated with an increased risk of thromboembolic events. Acute ischemic stroke is one of the common cerebrovascular complications linked to COVID-19.

Many studies have indicated that COVID-19-related stroke occurs in younger patients, with little to no risk factors. In addition, the majority of AIS patients with concomitant SARS-CoV-2 infection were elderly and had several cardiovascular complications. Cardiovascular risk factors were also found to enhance the risk of AIS.

Study Findings The study cohort included no patients with mild symptoms; 50% exhibited moderate symptoms, 37.5% had severe infections, and 12.5% were critically infected with SARS-CoV-2. Around 31% of the COVID-19 AIS group and 23.5% of the control group were treated with acute reperfusion therapy. Only severe-critical patients required ICU transfer, and their hospitalization duration was marginally longer compared to other groups.

Imaging data revealed that multiple vessel territorial involvement was similar in both COVID-19 AIS and non-COVID-19 AIS groups. A higher large vessel occlusion rate was found in the COVID-19 group, with larger anterior circulation LVO in the COVID-19 AIS group. Notably, in the COVID-19 AIS group, patients with pneumonia mainly exhibited higher LVO prevalence, which indicated a stronger association between COVID-19 pneumonia and LVO.

We have summarized this news so that you can read it quickly. If you are interested in the news, you can read the full text here. Read more:

NewsMedical /  🏆 19. in UK

United States Latest News, United States Headlines

Similar News:You can also read news stories similar to this one that we have collected from other news sources.

Autoantibodies against chemokines post-SARS-CoV-2 infection correlate with disease course - Nature ImmunologyAutoantibodies against chemokines post-SARS-CoV-2 infection correlate with disease course - Nature ImmunologyRobbiani and colleagues show that antibodies against specific chemokines are detected in COVID-19 convalescents and may modulate the inflammatory response and disease outcome.
Read more »

SARS-CoV-2 Antibody Dynamics in Healthcare Workers after mRNA VaccinationSARS-CoV-2 Antibody Dynamics in Healthcare Workers after mRNA VaccinationSince the emergence of SARS-CoV-2, maintaining healthcare worker (HCW) health and safety has been fundamental to responding to the global pandemic. Vaccination with mRNA-base vaccines targeting SARS-CoV-2 spike protein has emerged as a key strategy in reducing HCW susceptibility to SARS-CoV-2, however, neutralizing antibody responses subside with time and may be influenced by many variables. We sought to understand the dynamics between vaccine products, prior clinical illness from SARS-CoV-2, and incidence of vaccine-associated adverse reactions on antibody decay over time in HCWs at a university medical center. A cohort of 296 HCWs received standard two-dose vaccination with either bnt162b2 (Pfizer/BioNTech) or mRNA-1273 (Moderna) and were evaluated after two, six, and nine months. Subjects were grouped by antibody decay curve into steep antibody decliners gentle decliners. Vaccination with mRNA-1273 led to more sustained antibody responses compared to bnt162b2. Subjects experiencing vaccine-associated symptoms were more likely to experience a more prolonged neutralizing antibody response. Subjects with clinical SARS-CoV-2 infection prior to vaccination were more likely to experience vaccination-associated symptoms after first vaccination and were more likely to have a more blunted antibody decay. Understanding factors associated with vaccine efficacy may assist clinicians in determining appropriate vaccine strategies in HCWs.
Read more »

SGLT-2 inhibitors and in-stent restenosis-related events after acute myocardial infarction: an observational study in patients with type 2 diabetes - BMC MedicineSGLT-2 inhibitors and in-stent restenosis-related events after acute myocardial infarction: an observational study in patients with type 2 diabetes - BMC MedicineBackground No study evaluated the incidence of intra-stent restenosis (ISR)-related events in patients with type 2 diabetes (T2DM) and acute myocardial infarction (AMI) treated or not with sodium/glucose cotransporter 2 inhibitors (SGLT2i). Methods We recruited 377 patients with T2DM and AMI undergoing percutaneous coronary intervention (PCI). Among them, 177 T2DM were treated with SGLT2 inhibitors before PCI. The primary outcome was major adverse cardiovascular events (MACE) defined as cardiac death, re-infarction, and heart failure related to ISR. In patients without ISR, minimal lumen area and minimal lumen diameter were assessed by coronary CT-angiography at 1-year follow-up. Results Glycemic control was similar in SGLT2i-treated patients and never SGLT2i-users. The incidence of ISR-related MACE was higher in never SGLT2i-users compared with SGLT2i-treated patients, an effect independent of glycemic status (HR=0.418, 95% CI=0.241–0.725, P=0.002) and observed also in the subgroup of patients with HbA1c | 7% (HR=0.393, 95% CI=0.157–0.984, P=0.027). In patients without the event, the stent patency was greater in SGLT2i-treated patients compared with never SGLT2i-users at 1-year follow-up. Conclusions SGLT2i treatment in T2DM is associated with a reduced incidence of ISR-related events, independently of glycemic control.
Read more »

Organ and cell-specific biomarkers of Long-COVID identified with targeted proteomics and machine learning - Molecular MedicineOrgan and cell-specific biomarkers of Long-COVID identified with targeted proteomics and machine learning - Molecular MedicineBackground Survivors of acute COVID-19 often suffer prolonged, diffuse symptoms post-infection, referred to as “Long-COVID”. A lack of Long-COVID biomarkers and pathophysiological mechanisms limits effective diagnosis, treatment and disease surveillance. We performed targeted proteomics and machine learning analyses to identify novel blood biomarkers of Long-COVID. Methods A case–control study comparing the expression of 2925 unique blood proteins in Long-COVID outpatients versus COVID-19 inpatients and healthy control subjects. Targeted proteomics was accomplished with proximity extension assays, and machine learning was used to identify the most important proteins for identifying Long-COVID patients. Organ system and cell type expression patterns were identified with Natural Language Processing (NLP) of the UniProt Knowledgebase. Results Machine learning analysis identified 119 relevant proteins for differentiating Long-COVID outpatients (Bonferonni corrected P | 0.01). Protein combinations were narrowed down to two optimal models, with nine and five proteins each, and with both having excellent sensitivity and specificity for Long-COVID status (AUC = 1.00, F1 = 1.00). NLP expression analysis highlighted the diffuse organ system involvement in Long-COVID, as well as the involved cell types, including leukocytes and platelets, as key components associated with Long-COVID. Conclusions Proteomic analysis of plasma from Long-COVID patients identified 119 highly relevant proteins and two optimal models with nine and five proteins, respectively. The identified proteins reflected widespread organ and cell type expression. Optimal protein models, as well as individual proteins, hold the potential for accurate diagnosis of Long-COVID and targeted therapeutics.
Read more »

Autoantibodies against chemokines post-SARS-CoV-2 infection correlate with disease course - Nature ImmunologyAutoantibodies against chemokines post-SARS-CoV-2 infection correlate with disease course - Nature ImmunologyRobbiani and colleagues show that antibodies against specific chemokines are detected in COVID-19 convalescents and may modulate the inflammatory response and disease outcome.
Read more »

SARS-CoV-2 Antibody Dynamics in Healthcare Workers after mRNA VaccinationSARS-CoV-2 Antibody Dynamics in Healthcare Workers after mRNA VaccinationSince the emergence of SARS-CoV-2, maintaining healthcare worker (HCW) health and safety has been fundamental to responding to the global pandemic. Vaccination with mRNA-base vaccines targeting SARS-CoV-2 spike protein has emerged as a key strategy in reducing HCW susceptibility to SARS-CoV-2, however, neutralizing antibody responses subside with time and may be influenced by many variables. We sought to understand the dynamics between vaccine products, prior clinical illness from SARS-CoV-2, and incidence of vaccine-associated adverse reactions on antibody decay over time in HCWs at a university medical center. A cohort of 296 HCWs received standard two-dose vaccination with either bnt162b2 (Pfizer/BioNTech) or mRNA-1273 (Moderna) and were evaluated after two, six, and nine months. Subjects were grouped by antibody decay curve into steep antibody decliners gentle decliners. Vaccination with mRNA-1273 led to more sustained antibody responses compared to bnt162b2. Subjects experiencing vaccine-associated symptoms were more likely to experience a more prolonged neutralizing antibody response. Subjects with clinical SARS-CoV-2 infection prior to vaccination were more likely to experience vaccination-associated symptoms after first vaccination and were more likely to have a more blunted antibody decay. Understanding factors associated with vaccine efficacy may assist clinicians in determining appropriate vaccine strategies in HCWs.
Read more »



Render Time: 2025-02-26 08:19:40