Characterization of Hepatopathy in Turner Syndrome: Analysis of Determinants

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna

About this trial

The present study is therefore aimed at investigating the prevalence of hepatic alterations (laboratory and imaging) in adult patients with TS and generating hypothesissto the possible etiopathogenetic factors most involved, as well as evaluating the correlation between biochemical and structural abnormalities.

Thus, the study could provide relevant etiopathogenetic and prognostic results on the development of hepatopathy in TS patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of Turner syndrome made by karyotype analysis on peripheral blood.

Age 18 years or older

Written informed consent obtained

Disqualifiers

TS patients on therapy with drugs responsible for significant liver enzyme alterations (liver function alteration, LFA).

Trial population

The study population will be enrolled from the cohort of adult TS patients under longitudinal monitoring at the U.O.C. of Endocrinology and Diabetes Prevention and Care IRCCS Policlinico S. Orsola.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Factors associated with hepatopathy

Hepatopathy, defined as the presence of at least one of the following conditions: * AST ≥ 35 UI/L * ALT ≥ 35 UI/L * GGT ≥ 38 UI/L * ALP ≥ 116 UI/L * Presence of hepatic steatosis

Time frame
Baseline

Secondary outcomes

1

Comparison of liver morpho-functional parameters with results obtained by fibroscan.

Liver stiffness measurement (kPa)

Time frame
Baseline
2

Comparison of liver morpho-functional parameters with results obtained by fibroscan.

Spleen stiffnes measurement (kPa)

Time frame
Baseline

Other outcomes

Sponsors and contacts

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