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Barreira, D. P., Marinho, R. T., Bicho, M., Flores, I., Fialho, R. & Ouakinin, S. (2019). Hepatitis C pretreatment profile and gender differences: Cognition and disease severity effects. Frontiers in Psychology, 10. https://doi.org/10.3389/fpsyg.2019.02317

D. P. Barreira et al.,  "Hepatitis C pretreatment profile and gender differences: Cognition and disease severity effects", in Frontiers in Psychology, vol. 10, 2019

@article{barreira2019_1790988556165,
	author = "Barreira, D. P. and Marinho, R. T. and Bicho, M. and Flores, I. and Fialho, R. and Ouakinin, S.",
	title = "Hepatitis C pretreatment profile and gender differences: Cognition and disease severity effects",
	journal = "Frontiers in Psychology",
	year = "2019",
	volume = "10",
	number = "",
	doi = "10.3389/fpsyg.2019.02317",
	url = "https://www.frontiersin.org/journals/psychology"
}

TY  - JOUR
TI  - Hepatitis C pretreatment profile and gender differences: Cognition and disease severity effects
T2  - Frontiers in Psychology
VL  - 10
AU  - Barreira, D. P.
AU  - Marinho, R. T.
AU  - Bicho, M.
AU  - Flores, I.
AU  - Fialho, R.
AU  - Ouakinin, S.
PY  - 2019
SN  - 1664-1078
DO  - 10.3389/fpsyg.2019.02317
UR  - https://www.frontiersin.org/journals/psychology
AB  - Background: The hepatitis C virus (HCV) is known to infect the brain, however, the findings based on associated neuropsychiatric syndrome are controversial and the association itself remains unclear. Gender research in HCV infection is limited, failing to integrate the role of gender differences in neurocognitive syndrome. The aim of this study was to characterize psychological and neurocognitive profiles in HCV-infected patients before treatment and to explore gender differences in those profiles, as well as the impact of disease severity.
Methods: A total of 86 patients diagnosed with chronic hepatitis C were included. Depression and anxiety were assessed using Hamilton anxiety scale (HAM-A), Hamilton depression scale (HAM-D), Beck Depression Inventory (BDI). For cognition, a neuropsychological battery to measure attention, concentration and memory was used, and executive function components validated for the Portuguese population was also used before starting treatment. To identify the disease severity, platelet ratio index, and FibroScan® were used.
Results: A statistically significant gender effect was found on HAM-A (B = 0.64, CI: 0.17–1.11) and HAM-D (B = 0.62, CI: 0.14–1.09), with women scoring higher compared to men. Regarding neuropsychological scores, significant differences between gender were identified in executive functions measured by Trail Making Test (TMT B) (B = 0.48, CI: 0.02–0.97), TMT B-A (B = 0.26, CI: −39.2 to −3.7) and in digit span total (B = −0.52, CI: −1.0 to −0.04), with women performing worse than men. Controlling for years of substance dependence, TMT-B and TMT B-A showed significant gender differences. Regarding the presence or absence of substance dependence, only HAM-A and HAM-D remained significant. For categorical variables, Digit Span Total was also influenced by gender, with women being more likely to be impaired: odds ratio (OR) = 7.07, CI: 2.04–24.45), and a trend was observed for Digit Span Backward (OR = 3.57, CI: 1.31–9.75). No significant differences were found between disease severity and neurocognitive performance.
Conclusion: Data suggest that gender has an influence on depression, anxiety and cognitive functions with women showing greater impairment compared with men. This effect seems to be influenced by substance dependence.
ER  -