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1.
J Clin Rheumatol ; 27(1): 40-41, 2021 Jan 01.
Article in English | MEDLINE | ID: mdl-33347033

ABSTRACT

BACKGROUND/AIMS: A role for Helicobacter pylori in triggering systemic sclerosis (SSc) has been proposed, but data are conflicting. In previous studies, infection has been generally searched for by using serology. We designed this study to assess H. pylori prevalence in SSc patients with histology of gastric mucosa, considered the criterion standard for infection diagnosis. METHODS: This cross-sectional study enrolled 30 SSc patients who complained of upper gastrointestinal symptoms. All underwent upper endoscopy with gastric biopsies. Endoscopic alterations were recorded, and gastric mucosa biopsies were used for both histological examination and searching for H. pylori. The role for proton-pump inhibitor (PPI) therapy was considered. Fisher exact test was used for statistical analysis. RESULTS: Data of 28 SSc patients were available, 14 with ongoing PPI therapy. Helicobacter pylori infection at histology was detected in 14.3% patients, and it equally occurred in patients with or without PPI therapy. Erosive esophagitis/Barrett esophagus was detected in 26.6% of cases. Among patients with PPI therapy, 30% received half dose only. The prevalence of intestinal metaplasia was low (14.3%). Endoscopic esophageal alterations were significantly more frequent in those patients showing anti-Scl70 antibody positivity. CONCLUSIONS: This study showed that prevalence of H. pylori is very low in SSc patients, so that it seems not having a role in triggering SSc. Management of gastroesophageal diseases in SSc patients needs to be improved, and looking to the autoimmune profile may be of help. Thus, collaboration between rheumatologist and gastroenterologist is highly recommended.


Subject(s)
Helicobacter Infections/pathology , Helicobacter pylori/isolation & purification , Nuclear Proteins/immunology , Proton Pump Inhibitors/therapeutic use , Scleroderma, Systemic , Upper Gastrointestinal Tract , Autoantibodies/blood , Barrett Esophagus/pathology , Biopsy/methods , DNA Topoisomerases, Type I , Endoscopy, Digestive System/methods , Female , Gastric Mucosa/microbiology , Gastric Mucosa/pathology , Gastroesophageal Reflux/drug therapy , Helicobacter Infections/epidemiology , Humans , Male , Middle Aged , Risk Assessment , Scleroderma, Systemic/blood , Scleroderma, Systemic/diagnosis , Scleroderma, Systemic/microbiology , Scleroderma, Systemic/physiopathology , Upper Gastrointestinal Tract/diagnostic imaging , Upper Gastrointestinal Tract/microbiology , Upper Gastrointestinal Tract/pathology
2.
Int J Rheum Dis ; 24(4): 502-509, 2021 Apr.
Article in English | MEDLINE | ID: mdl-33073534

ABSTRACT

INTRODUCTION: Like other autoimmune diseases, systemic sclerosis (SSc) has been described to be associated with accelerated atherosclerosis (ATS). Before clinical manifestations of cardiovascular disease (CVD) occur, subclinical ATS can be investigated in different ways. AIM: To evaluate the presence of subclinical ATS in a group of patients with SSc, and to identify different risk profiles among patients. METHODS: Subclinical ATS was reviewed in 43 SSc patients and 27 healthy controls, using 2 methods: carotid ultrasound and flow mediated dilation (FMD) of the brachial artery. RESULTS: Plaques were statistically more frequent in SSc patients than in controls (65% vs 30%, P = .006); intima-media thickness of common carotid artery (CCA-IMT) resulted in statistically higher (median value 0.8 mm vs 0.55 mm; P < .0001) while FMD was significantly lower (median value 9% vs 14%; P = .0086) in patients compared to healthy controls. Among the SSc patients, thickening of CCA-IMT was significantly associated with the presence of diastolic dysfunction of left ventricle (absence of diastolic dysfunction: odds ratio [OR] 0.2, 95% CI 0.04-0.92, P = .038) and with a higher Framingham score (OR 1.3, 95% CI 1.03-1.6], P = .024). The diffuse cutaneous form was slightly protective against pathological FMD (OR 0.12, 95% CI 0.022-0.71, P = .019). CONCLUSIONS: This study confirms the involvement of macrocirculation in SSc patients, detecting the presence of subclinical ATS markers more frequently in patients compared to healthy controls. Framingham score, diastolic dysfunction of left ventricle and limited cutaneous form of the disease appeared to be associated with a higher risk of developing ATS.


Subject(s)
Atherosclerosis/etiology , Carotid Artery Diseases/etiology , Scleroderma, Systemic/complications , Aged , Asymptomatic Diseases , Atherosclerosis/diagnostic imaging , Atherosclerosis/physiopathology , Brachial Artery/diagnostic imaging , Brachial Artery/physiopathology , Carotid Artery Diseases/diagnostic imaging , Carotid Artery Diseases/physiopathology , Carotid Artery, Common/diagnostic imaging , Carotid Intima-Media Thickness , Case-Control Studies , Female , Humans , Male , Middle Aged , Plaque, Atherosclerotic , Risk Assessment , Risk Factors , Scleroderma, Systemic/diagnosis , Vasodilation
3.
Clin Rheumatol ; 40(4): 1393-1397, 2021 Apr.
Article in English | MEDLINE | ID: mdl-33188620

ABSTRACT

The outbreak of SARS-CoV-2 has changed the habits and lives of people worldwide. Patients affected by systemic sclerosis (SSc) experienced constant fear because of their immunocompromised status. The aim of this study was to investigate the prevalence of SARS-CoV-2 infection and to analyze the lifestyle changes in a single-center cohort of SSc patients and if these changes were more severe than in the general population. During the Italian lockdown, we supplied two surveys to our 184 SSc patients. In the first one, filled by 110 patients, we asked if SARS-CoV-2 had infected them or if they experienced signs and symptoms consistent with COVID-19. The second survey, performed by 79 SSc patients and 63 healthy subjects, included questions about the lifestyle adopted during this specific period. Among our patients, COVID-19 was diagnosed only in one case, while three other subjects reported signs and symptoms suggestive for the disease. Regarding the second survey, our patients greatly changed their lifestyle during the pandemic, adopting more restrictive isolation measures, because of their awareness of frailty. To date, we do not dispose of enough data to speculate about the risk of COVID-19 among immunocompromised patients, although in our SSc patients their frailty seems to have been their shelter. Pending more accurate epidemiological studies, it is essential to share as much data as possible to better understand the impact of COVID-19 on SSc patients' health. Key points • The lifestyle adopted by SSc patients during the first months of COVID-19 pandemic was characterized by more stringent isolation rules than general population. • The prudential behavior of patients with SSc during Italian lockdown should be considered as a possible bias when analyzing the risk of SARS-CoV-2 disease in these subjects, as well as a protective factor against infection.


Subject(s)
Life Style , Quarantine , Scleroderma, Systemic/psychology , Aged , COVID-19/epidemiology , COVID-19/psychology , Cohort Studies , Female , Humans , Italy , Male , Middle Aged , Surveys and Questionnaires
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