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1.
J Hepatol ; 80(1): 124-139, 2024 01.
Article in English | MEDLINE | ID: mdl-37730125

ABSTRACT

Gastrointestinal endoscopy has long been a reliable backbone in the diagnosis and management of hepatobilary disorders and their complications. However, with evolving non-invasive testing, personalised medicine has reframed the utility and necessity of endoscopic screening. Conversely, the growing interest and use of endoscopic ultrasound (EUS) and advanced endoscopy within gastrointestinal units has also opened novel diagnostic and therapeutic avenues for patients with various hepatobiliary diseases. The integration of "advanced endoscopy" within the practice of hepatology is nowadays referred to as "endo-hepatology". In essence, endo-hepatology consists of two pillars: one focusing primarily on disorders of the liver parenchyma, vascular disorders, and portal hypertension, which is mainly captured via EUS, while the other targets the hepatobiliary tract via endoscopic retrograde cholangiopancreatography and advanced imaging. Applications under the umbrella of endo-hepatology include, amongst others, EUS-guided liver biopsy, EUS-guided portal pressure gradient measurement, coil and glue embolisation of gastric varices as well as cholangioscopy. As such endo-hepatology could become an attractive concept wherein advanced endoscopy might reinforce the medical management of patients with hepatobiliary disorders and their complications after initial basic work-up. In this review, we discuss current trends and future developments within endo-hepatology and the remaining hurdles to overcome.


Subject(s)
Digestive System Diseases , Esophageal and Gastric Varices , Gastroenterology , Hypertension, Portal , Humans , Hypertension, Portal/diagnosis , Hypertension, Portal/therapy , Hypertension, Portal/complications , Esophageal and Gastric Varices/complications , Endoscopy, Gastrointestinal
2.
Transl Stroke Res ; 2023 Jul 20.
Article in English | MEDLINE | ID: mdl-37470917

ABSTRACT

Maladaptive inflammation underlies the formation and rupture of human intracranial aneurysms. There is a growing body of evidence that anti-inflammatory pharmaceuticals may beneficially modulate this process. Clopidogrel (Plavix) is a commonly used irreversible P2Y12 receptor antagonist with anti-inflammatory activity. In this paper, we investigate whether clopidogrel is associated with the likelihood of aneurysm rupture in a multi-institutional propensity-matched cohort analysis. Patients presenting for endovascular treatment of their unruptured intracranial aneurysms and those presenting with aneurysm rupture between 2015 and 2019 were prospectively identified at two quaternary referral centers. Patient demographics, comorbidities, and medication usage at the time of presentation were collected. Patients taking clopidogrel or not taking clopidogrel were matched in a 1:1 fashion with respect to location, age, smoking status, aneurysm size, aspirin usage, and hypertension. A total of 1048 patients with electively treated aneurysms or subarachnoid hemorrhages were prospectively identified. Nine hundred twenty-one patients were confirmed to harbor aneurysms during catheter-based diagnostic angiography. A total of 172/921 (19%) patients were actively taking clopidogrel at the time of presentation. Three hundred thirty-two patients were matched in a 1:1 fashion. A smaller proportion of patients taking clopidogrel at presentation had ruptured aneurysms than those who were not taking clopidogrel (6.6% vs 23.5%, p < .0001). Estimated treatment effect analysis demonstrated that clopidogrel usage decreased aneurysm rupture risk by 15%. We present, to the best of our knowledge, the first large-scale multi-institutional analysis suggesting clopidogrel use is protective against intracranial aneurysm rupture. It is our hope that these data will guide future investigation, revealing the pathophysiologic underpinning of this association.

3.
Phys Rev Lett ; 130(24): 240203, 2023 Jun 16.
Article in English | MEDLINE | ID: mdl-37390411

ABSTRACT

We propose relativistic tests of quantum gravity using the gravitational self-interaction of photons in a cavity. We demonstrate that this interaction results in a number of quantum gravitational signatures in the quantum state of the light that cannot be reproduced by any classical theory of gravity. We rigorously assess these effects using quantum parameter estimation theory and discuss simple measurement schemes that optimally extract their signatures. Crucially, the proposed tests are free of QED photon-photon scattering, are sensitive to the spin of the mediating gravitons, and can probe the locality of the gravitational interaction. These protocols provide a new avenue for studying the quantum nature of gravity in a relativistic setting.


Subject(s)
Photons , Quantum Theory
4.
Spine J ; 23(9): 1243-1254, 2023 09.
Article in English | MEDLINE | ID: mdl-37059306

ABSTRACT

Vertebral hemangiomas (VHs), formed from a vascular proliferation in bone marrow spaces limited by bone trabeculae, are the most common benign tumors of the spine. While most VHs remain clinically quiescent and often only require surveillance, rarely they may cause symptoms. They may exhibit active behaviors, including rapid proliferation, extending beyond the vertebral body, and invading the paravertebral and/or epidural space with possible compression of the spinal cord and/or nerve roots ("aggressive" VHs). An extensive list of treatment modalities is currently available, but the role of techniques such as embolization, radiotherapy, and vertebroplasty as adjuvants to surgery has not yet been elucidated. There exists a need to succinctly summarize the treatments and associated outcomes to guide VH treatment plans. In this review article, a single institution's experience in the management of symptomatic VHs is summarized along with a review of the available literature on their clinical presentation and management options, followed by a proposal of a management algorithm.


Subject(s)
Hemangioma , Spinal Neoplasms , Vertebroplasty , Humans , Hemangioma/surgery , Spine/surgery , Vertebroplasty/methods , Spinal Neoplasms/diagnosis
5.
Clin Neurol Neurosurg ; 226: 107613, 2023 03.
Article in English | MEDLINE | ID: mdl-36753862

ABSTRACT

BACKGROUND: Intracranial blister aneurysms are a rare and an historically difficult to treat subset of aneurysms. They are distinct from typical saccular aneurysms with different pathophysiology and treatment options. METHODS: A prospectively maintained database of subarachnoid hemorrhage patients was queried for those presenting prior to the pandemic (2017-2019), and those presenting during the height of the pandemic in our locality (2021). Aneurysm characteristics and patient demographics associated with rupture risk/formation were collected. RESULTS: 334 aneurysmal subarachnoid hemorrhage patients were reviewed. 86 of these patients presented in 2021, with a statistically significant increase in the proportion of ruptured ICA blister aneurysms as compared to 2017-2019 (7/86, 8% vs 5/248, p = .02). Mean patient age, presenting grade, other aneurysm location proportions, aneurysm size, and incidence of delayed cerebral ischemia were not different between the groups. CONCLUSIONS: Patients presenting with SAH during the height of the SARS-CoV-2 pandemic in 2021 were more likely to have ICA blister type aneurysms.


Subject(s)
Aneurysm, Ruptured , COVID-19 , Intracranial Aneurysm , Subarachnoid Hemorrhage , Humans , Pandemics , Prevalence , COVID-19/complications , SARS-CoV-2 , Intracranial Aneurysm/complications , Subarachnoid Hemorrhage/complications , Aneurysm, Ruptured/complications , Retrospective Studies , Cerebral Angiography/adverse effects
6.
Transl Stroke Res ; 13(4): 577-582, 2022 08.
Article in English | MEDLINE | ID: mdl-35028924

ABSTRACT

Current MR-vessel wall imaging (VWI) of unruptured intracranial aneurysms (UIAs) permits the visualization of wall structures. Aneurysm wall enhancement (AWE) was associated with atherosclerotic remodeling of the aneurysm wall accompanied by infiltration of inflammatory cells, potentially contributing to rupture. This study sought to investigate whether the luminal concentrations of atherosclerotic proteins in the aneurysm sac were associated with increased wall enhancement of UIAs in VWI. Subjects undergoing endovascular treatment for UIAs were prospectively recruited. All subjects underwent evaluation using 3 T-MRI including pre/post contrast VWI of the UIAs. Blood samples were collected from the aneurysm sac and the parent artery during endovascular procedures. The presence of AWE was correlated with the delta difference in concentration between the aneurysm sac and the parent artery for each atherosclerotic protein. A total of consecutive 45 patients with 50 UIAs were enrolled. The delta differences of anti-oxidized low-density lipoprotein (LDL) antibody, small dense LDL, and lipoprotein(a) [Lp(a)] were significantly higher in UIAs with AWE compared with those without AWE (767.6 ± 1957.1 versus - 442.4 ± 1676.3 mIU/mL, p = 0.02, 114.8 ± 397.7 versus - 518.5 ± 1344.4 µg/mL, p = 0.04, and - 5.6 ± 11.3 versus - 28.7 ± 38.5 µg/mL, p = 0.01, respectively). In multivariate logistic regression analysis, the delta Lp(a) was significantly associated with AWE (p = 0.04). Increased concentrations of atherogenic proteins in the aneurysm sac were significantly associated with wall enhancement of UIAs. Future studies examining the effect of medications for atherosclerosis on the atherogenic proteins within the aneurysm sac and hence the wall enhancement are warranted.


Subject(s)
Atherosclerosis , Intracranial Aneurysm , Atherosclerosis/diagnostic imaging , Cerebral Angiography/methods , Humans , Intracranial Aneurysm/complications , Intracranial Aneurysm/diagnostic imaging , Magnetic Resonance Imaging/methods
7.
Int J Mol Sci ; 22(19)2021 Oct 08.
Article in English | MEDLINE | ID: mdl-34639220

ABSTRACT

Interest in the use of pharmacological ascorbate as a treatment for cancer has increased considerably since it was introduced by Cameron and Pauling in the 1970s. Recently, pharmacological ascorbate has been used in preclinical and early-phase clinical trials as a selective radiation sensitizer in cancer. The results of these studies are promising. This review summarizes data on pharmacological ascorbate (1) as a safe and efficacious adjuvant to cancer therapy; (2) as a selective radiosensitizer of cancer via a mechanism involving hydrogen peroxide; and (3) as a radioprotector in normal tissues. Additionally, we present new data demonstrating the ability of pharmacological ascorbate to enhance radiation-induced DNA damage in glioblastoma cells, facilitating cancer cell death. We propose that pharmacological ascorbate may be a general radiosensitizer in cancer therapy and simultaneously a radioprotector of normal tissue.


Subject(s)
Ascorbic Acid/pharmacology , Hydrogen Peroxide/pharmacology , Neoplasms/radiotherapy , Oxidative Stress/drug effects , Radiation Tolerance/drug effects , Radiation-Sensitizing Agents/pharmacology , Animals , Antioxidants/pharmacology , Humans , Neoplasms/drug therapy , Neoplasms/pathology , Oxidants/pharmacology , Reactive Oxygen Species/metabolism
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