Publications by authors named "E Romeo"

Novel biomarkers are needed to better identify-and distinguish-heart failure with preserved ejection fraction (HFpEF) from other clinical phenotypes. The goal of our study was to identify epigenetic-sensitive biomarkers useful to a more accurate diagnosis of HFpEF. We performed a network-oriented genome-wide DNA methylation study of circulating CD4 T lymphocytes isolated from peripheral blood using reduced representation bisulfite sequencing (RRBS) in two cohorts (i.

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Pulmonary arterial hypertension (PAH) is defined as increase in mean pulmonary arterial pressure and pulmonary vascular resistance (PVR). It can be associated with congenital heart disease (CHD) with the following subtypes: 1) uncorrected left-to-right (L-R) intracardiac shunt leading to overload of the pulmonary circulation and a progressive increase of PVR; 2) Eisenmenger syndrome, appearing when a large post-tricuspid shunt is left uncorrected and pulmonary vascular disease (PVD) is severe, so the shunt becomes bidirectional or right-to-left, causing cyanosis; 3) PAH after shunt closure, when PVR arises after a defect correction; and 4) PAH associated with small or coincidental defects. While the treatment of patients with Eisenmenger syndrome is well established, the treatment of patients with PAH in whom there is a L-R shunt (with no cyanosis) remains unclear and requires expertise.

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Article Synopsis
  • Intestinal volvulus is a serious condition that can cause bowel obstruction and reduced blood flow to the intestines, potentially leading to death if not treated.
  • Symptoms of volvulus are often unclear but usually include sudden abdominal pain, distension, nausea, and vomiting.
  • A highlighted case in the article involves a patient who showed respiratory symptoms rather than typical gastrointestinal signs, making diagnosis challenging, with contrast-enhanced CT scans being the preferred diagnostic tool.
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Article Synopsis
  • In systemic sclerosis (SSc), severe aortic stenosis (AS) occurs in about 4.3% of patients, often linked to poor health outcomes and requiring careful monitoring.
  • In a study of 234 SSc patients from 2007 to 2022, ten had severe AS, with a notable progression rate over a mean period of 3.2 years, impacting heart function significantly.
  • Treatment options included transcatheter aortic valve implantation (TAVI) and surgical aortic valve replacement (SAVR), with most patients surviving long-term, highlighting the importance of screening for AS in SSc patients.
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Despite the innovations introduced in the 2022 European Society of Cardiology/European Respiratory Society Guidelines on Pulmonary Hypertension, risk discrimination and management of pulmonary arterial hypertension (PAH) patients at intermediate risk still represents a grey zone. Additionally, clinical evidence derived from currently available studies is limited. This expert panel survey intends to aid physicians in choosing the best therapeutic strategy for patients at intermediate risk despite ongoing oral therapy.

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