Need for awareness & surveillance of long-term #postCOVID neurodegenerative disorders. A position paper from the neuroCOVID‐19 task force of the European Academy of Neurology

https://link.springer.com/article/10.1007/s00415-025-13110-3

"An increase in the incidence of neurodegenerative diseases might be expected”

@longcovid
#LongCovid #PwLC #PostCovidSyndrome #LC #PASC #CovidBrain @covid19 #COVIDー19 #COVID19 #COVID #COVID_19 #SARSCoV2 @novid #novid @novid@a.gup.pe #CovidIsNotOver #auscovid19

Need for awareness and surveillance of long-term post-COVID neurodegenerative disorders. A position paper from the neuroCOVID‐19 task force of the European Academy of Neurology - Journal of Neurology

Background Neuropathological and clinical studies suggest that infection with SARS-CoV-2 may increase the long-term risk of neurodegeneration. Methods We provide a narrative overview of pathological and clinical observations justifying the implementation of a surveillance program to monitor changes in the incidence of neurodegenerative disorders in the years after COVID-19. Results Autopsy studies revealed diverse changes in the brain, including loss of vascular integrity, microthromboses, gliosis, demyelination, and neuronal- and glial injury and cell death, in both unvaccinated and vaccinated individuals irrespective of the severity of COVID-19. Recent data suggest that microglia play an important role in sustained COVID-19-related inflammation, which contributes to the etiology initiating a neurodegenerative cascade, to the worsening of pre-existing neurodegenerative disease or to the acceleration of neurodegenerative processes. Histopathological data have been supported by neuroimaging, and epidemiological studies also suggested a higher risk for neurodegenerative diseases after COVID-19. Conclusions Due to the high prevalence of COVID-19 during the pandemic, healthcare systems should be aware of, and be prepared for a potential increase in the incidence of neurodegenerative diseases in the upcoming years. Strategies may include follow-up of well-described cohorts, analyses of outcomes in COVID-19-registries, nationwide surveillance programs using record-linkage of ICD-10 diagnoses, and comparing the incidence of neurodegenerative disorders in the post-pandemic periods to values of the pre-pandemic years. Awareness and active surveillance are particularly needed, because diverse clinical manifestations due to earlier SARS-CoV-2 infections may no longer be quoted as post-COVID-19 symptoms, and hence, increasing incidence of neurodegenerative pathologies at the community level may remain unnoticed.

SpringerLink
Trump Fires Shira Perlmutter, Register of Copyrights and Director, U.S. Copyright Office

From Politico: President Donald Trump continued a firing spree at the Library of Congress on Saturday when he dismissed the top copyright official in the nation — a position traditionally overseen by the legislative branch. The White House contacted Register of Copyrights Shira Perlmutter Saturday afternoon informing her that her job leading the U.S. Copyright […]

Library Journal infoDOCKET
Habe HörmiCFC in einer Partie @LostCitiesApp in Grund und Boden gespielt #lc
#Trump limoge #CarlaHayden, directrice de la #BibliothèqueduCongrès #libraryofcongress #LC
https://actualitte.com/article/123695/international/trump-limoge-carla-hayden-directrice-de-la-bibliotheque-du-congres
Trump poursuit son entreprise de purge au sein de l'administration Sa dernière victime est Carla Hayden, nommée directrice de la Bibliothèque du Congrès par Barack Obama, en 2016 1ère femme, & 1ère personnalité afro-américaine à assumer cette fonction, Hayden a été visée pour ses positions libérales en matière d'accès aux ouvrages, à l'encontre du mouvement de censure des livres
Trump limoge Carla Hayden, directrice de la Bibliothèque du Congrès

Aux États-Unis, Donald Trump poursuit son entreprise de purge au sein de l'administration et des institutions publiques. Sa dernière victime en date n'est autre que Carla Hayden, nommée directrice de la Bibliothèque du Congrès par Barack Obama, en 2016. Première femme, mais aussi première personnalité afro-américaine à assumer cette fonction, Hayden a récemment été visée pour ses positions libérales en matière d'accès aux ouvrages, à l'encontre du mouvement de censure des livres encouragé par Trump.

ActuaLitté.com

Mitigating fatigue in long COVID patients with MYPplus: a clinical observation

https://bmcinfectdis.biomedcentral.com/articles/10.1186/s12879-025-10984-6

Screenshot is from the latest Science for ME weekly update

@longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC

Mitigating fatigue in long COVID patients with MYPplus: a clinical observation - BMC Infectious Diseases

Purpose The COVID-19 pandemic has led to the emergence of a secondary public health crisis known as Long COVID. It is estimated that approximately 10% of individuals who contact COVID-19 develop Long COVID, with fatigue and brain fog being among the most commonly reported and debilitating symptoms. However, no standardized or effective treatments are currently available. This observational study aimed to evaluate the efficacy of MYPplus, an herbal formulation composed of Astragali Radix, Salviae Radix, and Aquilariae Lignum, in alleviating fatigue and brain fog in patients with Long COVID. Methods Subjects with a score of 60 or higher on the Modified Korean version of the Chalder Fatigue scale (mKCFQ11) or a brain fog rating of 5 or higher on the visual analogue scale (VAS) took two capsules of MYPplus (500 mg per capsule) twice daily for 4 weeks. Changes in symptoms were assessed using the mKCFQ11, Multidimensional Fatigue Inventory (MFI-20), Fatigue VAS, Brain fog VAS, and overall quality of life using the Short-Form Health Survey (SF-12). Additionally, levels of three cytokines (TNF-α, TGF-β, IFN- γ) and cortisol were measured. Results Fifty participants successfully completed the 4-week administration with MYPplus. At baseline, fatigue severity was 75.3 ± 10.9 in mKCFQ11, 70.9 ± 11.2 in MFI-20, 7.5 ± 1.2 in Fatigue VAS, 8.4 ± 1.1 in Brain fog VAS, and 45.3 ± 17.8 in SF-12. All parameters significantly improved (p < 0.01), with a decrease of 46% in mKCFQ11, 26% in MFI-20, 49% in Fatigue VAS, and 52% in Brain fog VAS, and an increase of 59% in SF-12, respectively. Unlikely others, the plasma level of TGF-β showed a declining pattern after MYPplus administration (from 765.0 ± 1759.7 to 243.9 ± 708.1 pg/mL, p = 0.07). No safety concerns were observed. Conclusion This pilot observational study suggests the clinical potential of MYPplus for managing patients with Long COVID, focusing on fatigue-related symptoms and quality of life. Further studies are required to confirm its efficacy and safety using large-scale randomized placebo-controlled trials in the future. Protocol registration This study has been retrospectively registered with the identifier number KCT0008948 on https://cris.nih.go.kr , as of 27/10/23.

BioMed Central
Risk of post-acute symptoms among adults: A comparison study of severe COVID-19, pneumonia, and influenza

Background A retrospective cohort study was undertaken to assess the relationship between initial disease severity of COVID-19 and the risk of post-acute symptoms. The COVID-19 cohort was compared against influenza and pneumonia cohorts to assess whether risk of post-acute symptoms differed. Methods Administrative health claims data were obtained for commercially insured and Medicare Advantage covered adults (≥ 18 years) with symptomatic laboratory-confirmed COVID-19 diagnosed in 2020 (n=121,205), and similar cohorts of influenza (n=20,844) and pneumonia (n=29,052) patients diagnosed prior to the pandemic. Post-acute symptoms were assessed at four weeks, three and six months following initial diagnosis. Results Among the patients with COVID-19, the likelihood of any post-acute symptom increased with initial disease severity, and was also influenced by the presence of comorbidities, especially rheumatoid arthritis, ischemic heart disease and asthma. The specific post-acute symptoms varied by age, with increased risks of anxiety and headache among the young, whereas the elderly experienced increased brain fog and fatigue. When compared against the influenza and pneumonia cohorts, all three groups experienced post-acute symptoms, with a strong relationship to disease severity, and only partial resolution over the six-month observation period. Those with influenza were less likely than those with COVID-19 to experience post-acute symptoms while those with pneumonia were more likely to have post-acute illness than those with COVID-19. Conclusions Using a large national dataset, we found that COVID-19 symptomology could not be described by previously seen influenza or pneumonia symptomology and differences exist in the prevalence of symptoms as well as time to resolution, better characterizing “long COVID” and identifying that these differences are unique to COVID-19.

Trajectories of persisting Covid- 19 symptoms up to 24 months after acute infection: findings from the Predi-Covid cohort study - BMC Infectious Diseases

Introduction Long COVID is a multisystemic, fluctuating condition inducing a high burden on affected people. Despite the existence of some guidelines, its management remains complicated. We aimed to demonstrate that symptoms after a COVID-19 infection evolve following different trajectories from the initial infection until 24 months after, to identify the determinants of these trajectories, and the quality of life of people in these trajectories. Methods Study participants from the Predi-COVID cohort were digitally followed from their acute SARS-CoV-2 infection until a maximum of 24 months. Data from 10 common symptoms collected at study inclusion, and months 12, 15, and 24 awere used to create a total symptom score. Impact of symptoms on quality of life was assessed at month 24 using standardized questionnaires and ad-hoc questions. Latent classes mixed models were used to identify total score symptom trajectories and individual symptoms trajectories. Results We included 555 participants with at least 2 different time points available during follow-up (Baseline and at least one of the M12, M15 or M24 questionnaires). We identified 2 total symptom score trajectories: T1 “Mild symptoms, fast resolution” (N = 376; 67.7%), and T2 “Elevated and persisting symptoms” (N = 179; 32.3%). The main determinants of being in T2 were: older age (OR = 1.86; p = 0.003), to be a woman (OR = 1.81; p = 0.001)), elevated BMI (OR = 3.97; p < 0.001), and the presence of multi comorbidities (OR = 2.67; p = 0.005). Symptoms impacted the quality of life more in T2 than in T1 at 24 months (high fatigue level: 64.8% vs 19.5%, altered respiratory quality of life: 42.6% vs 4.6%, anxiety: 24.1% vs 4.6%, stress: 57.4% vs 35.6%, and bad sleep: 75.9% vs 51.1%). Conclusion A third of our study population was in the T2 “Elevated and persisting symptoms” trajectory, presenting high symptom frequencies up to 24 months after initial infection, with a significant impact on quality of life. This work underlined the urgent need to better identify individuals most vulnerable to long-term complications to develop tailored interventions for them. Trial registration Clinicaltrials.gov NCT04380987 (date of registration: 2020–05-07).

BioMed Central

From Sweden:

Complement activation was not increased in patients with post-acute sequelae after mild SARS-CoV-2 infection: A prospective cohort study

https://www.medrxiv.org/content/10.1101/2025.04.26.25326246v1

Screenshot is from the latest Science for ME weekly update

@longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC
@covid19 #Coronavirus
#COVID19 #COVID #COVID_19 #COVIDー19 #SARSCoV2 #CovidIsNotOver
@auscovid19 #auscovid19

Complement activation was not increased in patients with post-acute sequelae after mild SARS-CoV-2 infection: A prospective cohort study

Dysregulation of the complement system has been proposed as a pathophysiological mechanism for Post-acute sequelae of SARS-CoV-2 (PASC). We analyzed the complement activation markers C3bc, C3bBbP and TCC in 48 PASC patients, grouped into whether they had a mild (n=38) or severe (n=10) acute SARS-CoV-2 infection, and 80 control subjects. Although the patients with a mild SARS-CoV-2 infection had a trend towards more severe PASC, we could not find any significant differences in complement activation markers between these patients and controls. In conclusion, we could not find convincing evidence of activation of the complement system in PASC patients. ### Competing Interest Statement The authors have declared no competing interest. ### Funding Statement This study was supported by grants from Governmental Funds for Clinical Research (ALF), Interreg (EU), Sodra sjukvardsregionen, Skanes Universitetssjukhus, the Crafoord foundation, the Tegger Foundation and, the Alfred Osterlund Foundation all held by FK. MH was supported by grants from Sodra sjukvardsregionen. The funders played no role in the design of the study, data collection or analysis, decision to publish, or preparation of the manuscript. ### Author Declarations I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained. Yes The details of the IRB/oversight body that provided approval or exemption for the research described are given below: Ethics committee/IRB of Swedish Ethical Review Authority gave ethical approval for this work. I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals. Yes I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance). Yes I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable. Yes All data produced in the present study are available upon reasonable request to the authors

medRxiv
❤️‍🔥"Devoción" (Hannah Kent)

Traducido por: Laura Vidal
Pude leer este libro gracias a un préstamo interbibliotecario en el club de lectura de Mundo Forbit

La historia nos habla de Hanne, una adolescente que vive en una pequeña comunidad luterana en Prusia a principios del s.XIX
Es diferente al resto y no parece encajar, pero todo cambia cuando conoce a Thea
De quien se enamora perdidamente

Dicen que "Devoción" no es el mejor libro de la autora
Pero y yo, que me he maravillado con cada frase, con su ambientación, con la intensidad de un amor en un mundo duro y complejo, no sé cómo coño ha podido superarse en sus otras novelas
Sin duda, me ha atrapado, pienso seguir leyéndola y este libro ha pasado a ser uno de mis preferidos en la vida
¿Te animas a leerla tú?

#terecomiendo #reseñaliteraria #leoautoras #hannbakent #terecomiendo #LC