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1.
PLoS One ; 19(5): e0302383, 2024.
Article in English | MEDLINE | ID: mdl-38713724

ABSTRACT

Patients infected with herpes zoster might be at risk for Parkinson's disease (PD). However, antiviral drugs may impede viral deoxyribonucleic acid (DNA) synthesis. This study aimed to determine whether the currently observed association between herpes zoster and PD is consistent with previous findings, and whether antiviral drug use is associated with PD. This retrospective cohort study used the Longitudinal Generation Tracking Database. We included patients aged 40 years and above and applied propensity score matching at 1:1 ratio for study comparability. PD risk was evaluated using Cox proportional hazards regression methods. A total of 234,730 people were analyzed. The adjusted hazard ratio (aHR) for PD in patients with herpes zoster was 1.05. Furthermore, the overall incidence of PD was lower in those treated with antiviral drugs than in the untreated ones (3.17 vs. 3.76 per 1,000 person-years); the aHR was 0.84. After stratifying for sex or age, a similar result was observed. In conclusion, herpes zoster may increase the risk of PD, particularly among females, but receiving antiviral treatment reduces the risk by 16%. Therefore, using antiviral drugs may help prevent PD. However, additional research is required to determine the underlying mechanism(s).


Subject(s)
Antiviral Agents , Herpes Zoster , Parkinson Disease , Humans , Female , Male , Taiwan/epidemiology , Antiviral Agents/therapeutic use , Parkinson Disease/epidemiology , Parkinson Disease/drug therapy , Middle Aged , Aged , Incidence , Herpes Zoster/epidemiology , Herpes Zoster/drug therapy , Retrospective Studies , Adult , Proportional Hazards Models , Aged, 80 and over , Risk Factors
2.
J Biophotonics ; 14(3): e202000415, 2021 03.
Article in English | MEDLINE | ID: mdl-33231354

ABSTRACT

Cold atmospheric plasma (CAP) applications can potentially lead to effective therapy for numerous skin diseases. Our aim is to systematically review the available data and map the use of CAP in dermatology. PubMed, Embase and Web of science were explored before 2020 for studies regarding the use of CAP in dermatology. A total of 166 studies were finally included. 74.1% of these studies used indirect CAP sources. Most studies used plasma jet (67.5%). Argon was the mostly used working gas (48.2%). Plasma application itself could be direct (89.2%) and indirect (16.3%). The proportion of studies with in vivo results remained 57.2%, of which most concerned direct plasma treatment (97.9%). Analyses performed indicate that CAP has been beneficial in many skin disorders. While, most CAP applications were focused on wound healing and melanoma treatment. This study provides a brief overview of CAP sources and relative medical applications in dermatology.


Subject(s)
Dermatology , Plasma Gases , Skin Diseases , Humans , Plasma , Plasma Gases/therapeutic use , Skin Diseases/therapy , Wound Healing
3.
J Biomed Biotechnol ; 2011: 167395, 2011.
Article in English | MEDLINE | ID: mdl-21915163

ABSTRACT

Several variants of CTLA-4 have been reported to be associated with susceptibility systemic lupus erythematosus (SLE); however, findings have been inconsistent across different populations. Using a case-control study design, we have investigated the role of CTLA-4 polymorphism at positions -1661 and -1722 on SLE susceptibility in our Chinese SLE population in central China's Hubei province. Samples were collected from 148 SLE patients and 170 healthy controls. Polymerase chain reaction restriction fragments length polymorphism (PCR-RFLP) was used to analyze the genotypes of the two sites. Statistically significant difference was observed in genotypes for -1722, but not for -1661. The frequency of the T allele on the -1722 SNP was significantly increased in SLE patients: 57.8% versus 40.6% in controls (P < 0.001, OR = 2.002). While the detected C allele frequency in the controls was significantly elevated in comparison to that in the SLE patients (59.4% versus 42.2%). On the contrary, no association was found between SLE and CTLA-4 polymorphism at position -1661.


Subject(s)
CTLA-4 Antigen/genetics , Lupus Erythematosus, Systemic/genetics , Case-Control Studies , China/epidemiology , Female , Genetic Predisposition to Disease , Humans , Lupus Erythematosus, Systemic/epidemiology , Male , Odds Ratio , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Polymorphism, Single Nucleotide , Promoter Regions, Genetic
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