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1.
Cancers (Basel) ; 14(24)2022 Dec 08.
Article in English | MEDLINE | ID: mdl-36551539

ABSTRACT

(1) Background: While inequalities in the prevalence of cancer, access to care, and survival have been well documented, less research has focused on inequalities in the uptake of supportive oncology care. Given its contribution to improving the quality of life of people affected by cancer, access to such care is a major public health issue. The present study focuses on the access and uptake of those supportive oncology care services. (2) Methods: This study is based on qualitative research methodology, using a thematic analysis tree on NVivo© analysis software. First, an exploratory survey was conducted with users of oncology services, and professionals from these services and supportive oncology care. Then, individual interviews were conducted in June 2022 among people who are currently being treated or have been treated for cancer. (3) Results: The experiences of the 33 respondents revealed that significant variations in the uptake of supportive oncology care are underpinned by identifiable disparities in their healthcare pathways: in their assimilation of information, difficulties in accessing oncology care, personal reluctance and motivations, perceived needs and benefits, and use of other medicines. (4) Conclusion: This study aims to gain some insight into disparities in the uptake of supportive care in the Centre-Val de Loire region (France). Thus, it provides a better understanding of the complex ways in which these inequalities in supportive oncology care uptake are constructed.

2.
Transl Psychiatry ; 10(1): 409, 2020 Nov 24.
Article in English | MEDLINE | ID: mdl-33235192

ABSTRACT

A Correction to this paper has been published: https://doi.org/10.1038/s41398-020-01102-y.

3.
Transl Psychiatry ; 10(1): 213, 2020 07 03.
Article in English | MEDLINE | ID: mdl-32620743

ABSTRACT

Recent evidence showing degeneration of the noradrenergic system in the locus coeruleus (LC) in Alzheimer's disease (AD) has motivated great interest in noradrenaline (NA) as a potential brain hallmark of the disease. Despite the current exploration of blood markers for AD, the deregulation of the plasma NA concentration ([NA]plasma) in AD is currently not well understood. This retrospective study includes a cohort of 71 patients (32 AD patients, 22 with other dementia and 17 without dementia) who were given consultations for memory complaints in the Cognitive Neurology Center of Lariboisière (Paris) between 2009 and 2014. As previously described in brain tissue, we show for the first time a linear correlation between [NA]plasma and Mini Mental State Examination (MMSE) score in AD patients. We observed that high [NA]plasma in AD patients was associated with higher [Aß1-42]CSF than in other AD patients with [NA]plasma similar to NC patients. In parallel, we observed a lower (p-Tau/Tau)CSF in AD patients with low [NA]plasma than in non-AD patients with [NA]plasma similar to [NA]plasma in NC patients. Our data suggest that [NA]plasma could be a potential biomarker of disease evolution in the context of AD and could possibly improve early diagnosis.


Subject(s)
Alzheimer Disease , Amyloid beta-Peptides , Biomarkers , Cognition , Humans , Norepinephrine , Peptide Fragments , Retrospective Studies , tau Proteins
4.
J Neurol ; 263(6): 1111-9, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27060084

ABSTRACT

To report on OPTIPUMP, a cohort study, investigating the impact in real-life clinical settings of continuous subcutaneous apomorphine infusion (CSAI) on the quality of life (HRQoL) of patients with Parkinson's disease. OPTIPUMP was a prospective, open-label, observational cohort study involving 30 investigational sites in France. CSAI was proposed as part of routine clinical care to patients aged ≥18 years, in absence of dementia, with a PD diagnosis and based on the presence of motor fluctuations not controlled by oral treatments. The impact of APO-pump on quality of life was evaluated as the difference in PDQ-39 scores between the initiation treatment and the follow-up visit after 6 months' treatment. All adverse events were recorded. Hyper- and hypodopaminergic behavioral tolerance was assessed on the Ardouin Scale of Behavior in Parkinson's Disease. Between September 2011 and January 2013, we enrolled 142 patients: 42 patients were withdrawn due to pump removal (33), death (4), lost of follow-up (4), no available data (1). 100 completed the study. At 6 months, their HRQoL had significantly improved (p = 0.011), as had their total UPDRS score (p < 0.001). Regarding the safety profile, Ardouin scale scores indicated that their hyperdopaminergic behaviors had not increased. CSAI had a favorable impact on HRQoL, with benefits outweighing risks. The analysis of the withdrawn patients highlights the heterogeneity of the use of the pump having an impact on its efficacy and tolerability.


Subject(s)
Antiparkinson Agents/administration & dosage , Apomorphine/administration & dosage , Dopamine Agonists/administration & dosage , Infusion Pumps , Parkinson Disease/drug therapy , Quality of Life , Aged , Antiparkinson Agents/adverse effects , Apomorphine/adverse effects , Dopamine Agonists/adverse effects , Female , Follow-Up Studies , France , Humans , Infusion Pumps/adverse effects , Infusions, Subcutaneous/adverse effects , Male , Parkinson Disease/psychology , Prospective Studies , Treatment Outcome
6.
Microbes Infect ; 9(1): 47-54, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17196420

ABSTRACT

Gliotoxin is a mycotoxin having a considerable number of immuno-suppressive actions and is produced by several moulds such as Aspergillus fumigatus. In this study, we investigated its toxic effects on human neutrophils at concentrations corresponding to those found in the blood of patients with invasive aspergillosis. Incubation of the cells for 10min with 30-100ng/ml of gliotoxin inhibited phagocytosis of either zymosan or serum-opsonized zymosan without affecting superoxide production or the exocytosis of specific and azurophil granules. Gliotoxin also induced a significant re-organization of the actin cytoskeleton which collapsed around the nucleus leading to cell shrinkage and the disappearance of filopodia. This gliotoxin-induced actin phenotype was reversed by the cAMP antagonist Rp-cAMP and mimicked by pCPT-cAMP indicating that it probably resulted from the deregulation of intracellular cAMP homeostasis as previously described for gliotoxin-induced apoptosis. By contrast, gliotoxin-induced inhibition of phagocytosis was not reversed by Rp-cAMP but by arachidonic acid, another member of a known signalling pathway affected by the toxin. This suggests that gliotoxin can affect circulating neutrophils and favour the dissemination of A. fumigatus by inhibiting phagocytosis and the consequent killing of conidia.


Subject(s)
Actins/metabolism , Aspergillus fumigatus/metabolism , Cytoskeleton/drug effects , Gliotoxin/toxicity , Neutrophils/drug effects , Phagocytosis/drug effects , Actins/physiology , Arachidonic Acid/metabolism , Aspergillosis/immunology , Aspergillosis/metabolism , Aspergillosis/microbiology , Aspergillus fumigatus/chemistry , Aspergillus fumigatus/immunology , Cyclic AMP/metabolism , Cytoskeleton/metabolism , Gliotoxin/immunology , Gliotoxin/isolation & purification , Gliotoxin/metabolism , Humans , NADPH Oxidases/metabolism , Neutrophils/enzymology , Neutrophils/immunology , Neutrophils/metabolism , Phagocytosis/immunology , Signal Transduction/drug effects
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