Carolina Castagnetti

Prof. Dr. Carolina Castagnetti

orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2010 in Theriogenology
Verified
Journal Article
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CCCarolina Castagnetti
Carolina Castagnetti
APA. Pirrone
A. Pirrone
JMJ. Mariella
J. Mariella
GMG. Mari
G. Mari

21 June 2018 in Equine Veterinary Journal
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Journal Article
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SQS. Quercia
S. Quercia
FFFrancesca Freccero
Francesca Freccero
CCCarolina Castagnetti
Carolina Castagnetti
MSM. Soverini
M. Soverini
STS. Turroni
S. Turroni
MCMarco Candela
Marco Candela

1 December 2012 in Research in Veterinary Science
Verified
Journal Article
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EIEleonora Iacono
Eleonora Iacono
BMBarbara Merlo
Barbara Merlo
APA. Pirrone
A. Pirrone
CAC. Antonelli
C. Antonelli
LBL. Brunori
L. Brunori
CCCarolina Castagnetti
Carolina Castagnetti

1 September 2012 in American Journal of Veterinary Research
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Journal Article
Closed access
CCCarolina Castagnetti
Carolina Castagnetti
JMJole Mariella
Jole Mariella
APAlessandro Pirrone
Alessandro Pirrone
SCStefano Cinotti
Stefano Cinotti
GMGaetano Mari
Gaetano Mari
APAngelo Peli
Angelo Peli
Objective—To evaluate and compare the gene expression of interleukin(IL)-1β, IL-8, and interferon-γ during the first 72 hours after birth in healthy foals and during the first 72 hours after hospitalization in sick neonatal foals and investigate correlations of clinicopathologic variables with cytokine expressions in healthy and sick neonatal foals. Animals—33 foals < 7 days old (10 healthy foals, 7 foals with sepsis, 6 foals with peripartum asphyxia syndrome, and 12 foals with other diseases [2 with failure of passive transfer of immunity only were not further evaluated]). Procedures—A blood sample (15 mL) was collected from each foal immediately after birth or hospital admission (0 hours) and at 24 and 72 hours later. Clinicopathologic variables were evaluated, and cytokine gene expression in WBCs was measured with an absolute quantitative real-time reverse transcriptase PCR assay. Results—At all time points, gene expression of interferon-γ was low in all groups. No time-dependent changes in cytokine expressions were detected in healthy or sick foals. Foals with sepsis had significantly higher IL-1β gene expression than did healthy foals, foals with peripartum asphyxia syndrome, or foals with other diseases. At 0 hours, IL-1β expression was correlated with plasma fibrinogen concentration in healthy foals and with the neutrophil-to-lymphocyte ratio in foals with sepsis; IL-8 expression was correlated with monocyte count in foals with sepsis and with arterial pH, plasma fibrinogen concentration, and plasma lactate concentration in foals with peripartum asphyxia syndrome. Conclusions and Clinical Relevance—Data have suggested that evaluation of IL-1β expression in sick neonatal foals could help identify those with sepsis.

8 June 2022 in Animals
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Journal Article
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ALALIAI LANCI
ALIAI LANCI
FPFrancesca Perina
Francesca Perina
ADAndré Donadoni
André Donadoni
CCCarolina Castagnetti
Carolina Castagnetti
JJole Mariella
Jole Mariella
Dystocia as a prolonged stage II parturition (>30 min) was associated with a higher risk of complications. The hypothesis of the study was that any type of dystocia could affect the foal’s health, even when the stage II was <30 min. Clinical reports on 222 Standardbred mares and their foals hospitalized at the Veterinary Teaching Hospital of the University of Bologna from 2004 to 2020 were reviewed. Mares were divided into the Eutocia Group (165, eutocic delivery) and the Dystocia Group (57, dystocic delivery). The incidence of dystocia was 4.9%. Stage II was longer in the Dystocia Group (median 20 min) than in the Eutocia Group (median 12 min). All occurrences of dystocia were retrospectively classified into three categories of severity: mild, moderate and severe dystocia. The occurrence of postpartum complications in mares and neonatal diseases and failure of passive transfer of immunity in foals was higher in the Dystocia Group. Foal venous lactatemia and serum creatine kinase were significantly higher in the Dystocia Group (median 3.9 mmol/L; 262 UI/L respectively) than in the Eutocia Group (median 3.1 mmol/L; 187 UI/L respectively). The APGAR score was lower in the Dystocia Group (median 8) than in the Eutocia Group (median 10) and significantly lower in severe dystocia (median 3). The duration of stage II should not be considered the only parameter of dystocia in mares: even a rapid resolution of dystocia could pose health risks to the foal and the mare.

15 May 2021 in Animals
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Journal Article
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GSGiuseppe Sarli
Giuseppe Sarli
CCCarolina Castagnetti
Carolina Castagnetti
CBCarlo Bianco
Carlo Bianco
GBGiulia Ballotta
Giulia Ballotta
GTGiorgia Tura
Giorgia Tura
DZDANIELE ZAMBELLI
DANIELE ZAMBELLI
Placenta is essential for the development of the fetus, and its impaired function can lead to a negative outcome (i.e., neonatal mortality). In dogs, investigations on placenta histology and neonatal outcome in healthy bitches are lacking, and a contribution is provided in this study to emphasize the use of placenta histology in practice. Fifty-one placentas from 11 litters were collected during cesarean section, classified according to the litter size (large (L) or small (S)) and the outcome, this latter as healthy (Group 1) or dead within 7 days (Group 2). The placenta/puppy weight ratio (PPR) was calculated, and specimens were formalin-fixed and paraffin-wax embedded, and on the resulting histological slides, capillary density (CD) was quantified. Among necrosis, calcification, and intravascular leucocytes, only the presence of multifocal-confluent necrosis (significantly more frequent in Group 2) was associated with a higher risk of death within 7 days (odds ratio = 30.7). Mixed logistic regression ruled out the effect on death both of a bitch and cesarean type (programmed vs. emergency). PPR and CD values were associated with litter size; large litters had lower PPR (p < 0.01) and higher CD (p < 0.05) than small litters. The relationship between PPR and CD was negative and significant (p < 0.01). Necrosis was a frequent finding in canine placentas, but only when multifocal-confluent was it associated with a poor outcome. The litter size influenced PPR (lower in L) and CD (higher in L), and this is likely due to the plasticity of placenta adaptation.