4.4 Article

The Activity of Malignancy May Determine Stroke Pattern in Cancer Patients

Journal

JOURNAL OF STROKE & CEREBROVASCULAR DISEASES
Volume 24, Issue 4, Pages 778-783

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jstrokecerebrovasdis.2014.11.003

Keywords

Etiology; malignancy; outcome; prothrombotic; risk factors; stroke

Funding

  1. Polish National Ministry of Education and Science [NN402 085334]

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Background: It has been suggested that stroke in patients with cancer may differ from the conventional pattern. The aim of this study was to evaluate the burden of vascular risk factors, stroke etiology, and short-term outcome in patients with active and nonactive malignancy compared with patients without cancer. Methods: This is a prospective cohort study of consecutive acute stroke patients admitted to our department between September 2006 and September 2011. We distinguished between the following: (1) patients with active malignancy (AM, diagnosed not earlier than 12 months before stroke); (2) patients with nonactive malignancy (non-AM); and (3) cancer-free (CF) patients, used as a reference. Results: Pre-existing cancer was found in 90 of 1558 patients, including 41 (2.6%) cases with AM and 49 (3.1%) cases with non-AM. Compared with CF patients, AM patients less frequently had a history of previous stroke (2.4% versus 17.9%, P = .018) and more frequently experienced ischemic strokes of undetermined etiology (62.5% versus 38.3%, P = .002). Non-AM patients did not differ in the distribution of vascular risk factors but more often experienced stroke caused by small vessel occlusion (20.0% versus 8.0%, P = .004). Inflammatory blood markers were elevated especially in patients with AM. Short-term prognosis was similar across all groups. Conclusions: Stroke pattern in patients with non-AM appears very similar to that observed in the CF patients. However, our findings support the thesis that cancer-specific prothrombotic mechanisms play an important role in stroke patients with AM, which may be related to active inflammatory and immune processes. Malignancy does not influence short-term prognosis of stroke.

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Summary: This retrospective study evaluated the safety and outcomes of revascularization treatments in patients with acute ischemic stroke and COVID-19. COVID-19 patients had higher rates of intracranial bleeding complications and worse clinical outcomes after treatment compared to non-COVID-19 patients.

NEUROLOGY (2023)

Article Biochemistry & Molecular Biology

A Century of Progress on Wilson Disease and the Enduring Challenges of Genetics, Diagnosis, and Treatment

Louis C. Penning, Marina Berenguer, Anna Czlonkowska, Kay L. Double, Petr Dusek, Carmen Espinos, Svetlana Lutsenko, Valentina Medici, Wiebke Papenthin, Wolfgang Stremmel, Jose Willemse, Ralf Weiskirchen

Summary: Wilson disease is a rare inherited metabolic disorder with diverse clinical presentations affecting the liver, neurological system, psychiatric status, and vision, often in combination. Mutations in the ATP7B gene lead to copper accumulation in hepatocytes and/or neurons, making clinical diagnosis challenging. Diagnosis is complicated by mild and non-specific manifestations, mutations with unclear effects on protein function, and ambiguous laboratory tests, particularly concerning serum ceruloplasmin levels. Establishing a global collaboration of researchers, clinicians, and patient advocacy groups is crucial for identifying and addressing the outstanding challenges of Wilson disease.

BIOMEDICINES (2023)

Article Clinical Neurology

Reliability of the modified Rankin Scale in clinical practice of stroke units and rehabilitation wards

Natalia Pozarowszczyk, Iwona Kurkowska-Jastrzebska, Iwona Sarzynska-Dlugosz, Maciej Nowak, Michal Karlinski

Summary: The aim of this study was to assess the consistency between neurologists and physical and rehabilitation medicine physicians in using the Modified Rankin Scale (mRS) to rate post-stroke disability. The results showed a modest agreement in using mRS, but it may be considered sufficient for observational studies or stroke registries.

FRONTIERS IN NEUROLOGY (2023)

Review Medicine, General & Internal

Blood Based Biomarkers of Central Nervous System Involvement in Wilson's Disease

Agnieszka Antos, Anna Czlonkowska, Jan Bembenek, Marta Skowronska, Iwona Kurkowska-Jastrzebska, Tomasz Litwin

Summary: Wilson's disease is an inherited disorder of copper metabolism that can cause hepatic and/or neuropsychiatric symptoms. Early diagnosis and anti-copper treatment are key for a favorable outcome. New treatment modalities are being sought to prevent neurological deterioration. Serum biomarkers are important for disease management, and there is a need for blood-based biomarkers for central nervous system (CNS) injury.

DIAGNOSTICS (2023)

Article Clinical Neurology

Effects of blood pressure and tranexamic acid in spontaneous intracerebral haemorrhage: a secondary analysis of a large randomised controlled trial

Jason Philip Appleton, Zhe Kang Law, Lisa Jane Woodhouse, Rustam Al-Shahi Salman, Maia Beridze, Hanne Christensen, Robert A. Dineen, Juan Jose Egea Guerrero, Timothy J. England, Michal Karlinski, Kailash Krishnan, Ann Charlotte Laska, Philippe Lyrer, Serefnur Ozturk, Christine Roffe, Ian Roberts, Thompson G. Robinson, Polly Scutt, David J. Werring, Philip M. Bath, Nikola Sprigg

Summary: In the TICH-2 trial, patients with acute spontaneous intracerebral hemorrhage were divided into two groups based on baseline systolic blood pressure. The results showed that patients with a baseline SBP ≤170 mm Hg had better clinical and radiological outcomes after receiving tranexamic acid.

BMJ NEUROLOGY OPEN (2023)

Review Medicine, General & Internal

Copper Deficiency as Wilson's Disease Overtreatment: A Systematic Review

Tomasz Litwin, Agnieszka Antos, Jan Bembenek, Adam Przybylkowski, Iwona Kurkowska-Jastrzebska, Marta Skowronska, Anna Czlonkowska

Summary: This systematic review examines the occurrence of copper deficiency (CD) in Wilson's disease (WD) patients during treatment. CD diagnosis is based on symptoms and blood tests, and regular monitoring of copper metabolism is necessary during treatment. Temporary cessation of anti-copper treatment can usually reverse serum copper reductions seen in CD.

DIAGNOSTICS (2023)

Review Biology

D-Penicillamine-Induced Myasthenia Gravis-A Probable Complication of Wilson's Disease Treatment-A Case Report and Systematic Review of the Literature

Agnieszka Antos, Anna Czlonkowska, Jan Bembenek, Iwona Kurkowska-Jastrzebska, Tomasz Litwin

Summary: Wilson's disease is a genetic disorder that causes copper accumulation in various tissues, leading to clinical symptoms. D-penicillamine (DPA) is a commonly used drug in its treatment, but it can also induce myasthenia gravis (MG). This case report discusses a patient with WD who developed symptoms of MG after 15 months of DPA treatment.

LIFE-BASEL (2023)

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