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1.
Curr Rev Clin Exp Pharmacol ; 17(2): 156-160, 2022.
Article in English | MEDLINE | ID: mdl-34477542

ABSTRACT

BACKGROUND: Hepatitis C Virus (HCV) infection represents a global problem, and it is related to both hepatic and extra-hepatic manifestations (e.g., xerophthalmia). New direct-acting antivirals (DAAs), IFN-free treatments, are commonly used to manage HCV infection. However, the impact of new DAAs on dry eyes (xerophthalmia) is lacking. In this study, we evaluated its incidence in HCV patients and the effect of DAAs on this manifestation. METHODS: We performed an observational open-label non-randomized study in HCV patients from 01 April 2018 to 01 June 2020. RESULTS: Patients who satisfied the inclusion criteria underwent clinical and laboratory evaluation, Schirmer's test, and Break-up time test. Enrolled patients were divided in two groups: Group 1: HCV patients with xerophthalmia: 24 patients (16 male and 8 female), HCV-RNA 2,685,813 ± 1,145,698; Group 2: HCV patients without xerophthalmia: 35 patients (19 male and 16 female), HCV-RNA 2,614,757 ± 2,820,433. The follow-ups (3 and 6 months after the enrollment) documented an improvement in both eyes' manifestations and HCV-infection (HCV-RNA undetected). CONCLUSION: In conclusion, in this study, we reported that xerophthalmia could appear in HCV patients, and DAAs treatment reduces this manifestation without the development of adverse drug reactions.


Subject(s)
Hepatitis C, Chronic , Hepatitis C , Xerophthalmia , Antiviral Agents/therapeutic use , Female , Hepacivirus/genetics , Hepatitis C/complications , Hepatitis C, Chronic/complications , Humans , Male , RNA/pharmacology , Xerophthalmia/chemically induced
2.
J Matern Fetal Neonatal Med ; 34(10): 1679-1682, 2021 May.
Article in English | MEDLINE | ID: mdl-31315488

ABSTRACT

PURPOSE: To evaluate the relation between CD34+ cells count in maternal blood and potential development of fetal congenital renal abnormalities. MATERIALS AND METHODS: We enrolled 16 women that gave birth to newborns carrying congenital renal malformations over a 3-year period and 48 women with uncomplicated pregnancies (controls) in a 1:3 ratio (three controls per case). RESULTS: CD34+ cells in the maternal peripheral blood were significantly lower in the group of women who gave birth to newborns carrying congenital renal malformations compared to the controls (p < .0001). CONCLUSIONS: CD34+ cells in maternal blood could be validated as a potential marker to predict the development of possible kidney malformations.


Subject(s)
Congenital Abnormalities , Fetus , Case-Control Studies , Female , Fetal Blood , Humans , Infant, Newborn , Kidney , Pregnancy
3.
Ther Apher Dial ; 24(3): 258-264, 2020 Jun.
Article in English | MEDLINE | ID: mdl-31483921

ABSTRACT

The mechanism of action of fibroblast growth factor-23 (FGF23) is becoming increasingly clearer as a result of studies that have defined its structure and pleiotropic effects. Furthermore, data are emerging on the effects exerted on this hormone by iron administration. Ten main iron formulations are recognized (with clear differences in composition and possible reactions of intolerance and anaphylaxis), which are indicated for iron deficiency anemia, including nephropathic subjects, as suggested by medical guidelines. With some types of iron formulation (especially iron carboxymaltose) a particular side effect has been observed: hypophosphatemia, mediated by FGF23. This review aims to draw attention to this correlation and the contradiction represented by the presence of both positive and negative modulation by FGF23, with the effects induced by its increase even after long-term treatment with iron formulation. However, more evidence is needed to understand the reasons for this differential stimulation.


Subject(s)
Anemia, Iron-Deficiency/drug therapy , Drug-Related Side Effects and Adverse Reactions , Ferric Compounds/pharmacology , Fibroblast Growth Factor-23/metabolism , Hypophosphatemia , Maltose/analogs & derivatives , Drug-Related Side Effects and Adverse Reactions/metabolism , Drug-Related Side Effects and Adverse Reactions/prevention & control , Hematinics/pharmacology , Humans , Hypophosphatemia/chemically induced , Hypophosphatemia/metabolism , Hypophosphatemia/prevention & control , Long Term Adverse Effects/prevention & control , Maltose/pharmacology
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