Evidence map›Paper›PMID 41795218›Full record

Observational studyEuropean journal of clinical investigation2026

Infectious seeds of valve calcification: Exploring the bacterial hypothesis in the pathogenesis of calcific aortic valve disease.

Antonella Forlino, Paola Giordani, Cristina Merla, Silvia Roda, Roberta Besio, Abeer Ahmed Qaed Ahmed, Angela Kuka, Irene Mileto, Greta Petazzoni, Marta Corbella and 12 more

Abstract readObservational Study
In one paragraph

Observational study in European journal of clinical investigation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

Antonella ForlinoDepartment of Molecular Medicine, Biochemistry Unit, University of Pavia, Pavia, Italy.ORCID https://orcid.org/0000-0002-6385-1182
Paola GiordaniMalattie Infettive, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0009-0000-5507-3803
Cristina MerlaMicrobiologia e Virologia, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0000-0003-2986-6644
Silvia RodaInfectious Diseases Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.ORCID https://orcid.org/0000-0002-0710-174X
Roberta BesioDepartment of Molecular Medicine, Biochemistry Unit, University of Pavia, Pavia, Italy.ORCID https://orcid.org/0000-0003-1430-2934
Abeer Ahmed Qaed AhmedDepartment of Molecular Medicine, Biochemistry Unit, University of Pavia, Pavia, Italy.
Angela KukaMicrobiologia e Virologia, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0009-0007-5134-5526
Irene MiletoMicrobiologia e Virologia, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0009-0007-5272-3138
Greta PetazzoniMicrobiologia e Virologia, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0000-0003-3537-8006
Marta CorbellaMicrobiologia e Virologia, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0000-0002-0969-6484
Patrizia CambieriMicrobiologia e Virologia, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Baldanti FaustoMicrobiologia e Virologia, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0000-0002-6899-3462
Annalisa De SilvestriBiostatistics and Clinical Epidemiology, Fondazione IRCCS Policlinico san Matteo, Pavia, Italy.ORCID https://orcid.org/0000-0003-3128-8441
Totaro PasqualeCardiac Surgery Unit, Fondazione IRCCS Policlinico san Matteo, Pavia, Italy.ORCID https://orcid.org/0000-0002-5403-6274
Filippo AmorosoCardiac Surgery Unit, Fondazione IRCCS Policlinico san Matteo, Pavia, Italy.ORCID https://orcid.org/0009-0008-5552-8116
Pelenghi StefanoCardiac Surgery Unit, Fondazione IRCCS Policlinico san Matteo, Pavia, Italy.
Maraschi FedericaDepartment of Chemistry, University of Pavia, Pavia, Italy.ORCID https://orcid.org/0000-0002-7895-5291
Eloisa ArbustiniDepartment of Research, Centre for Inherited Cardiovascular Diseases, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0000-0003-2948-7994
Viviana VilardoDepartment of Research, Centre for Inherited Cardiovascular Diseases, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0009-0009-0493-0938
Alexandra SmirnovaDepartment of Research, Centre for Inherited Cardiovascular Diseases, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0000-0002-8911-8827
Raffaele BrunoMalattie Infettive, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0000-0002-0235-9207
Seminari ElenaMalattie Infettive, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0000-0001-5246-928X

Funding

Ministero della Salute 08072322Ministero della Salute 2022 23683266Ministero della Salute E03 2022 23683266 DIAGNOSTICA AVANZATA - (HLS-DA)
6 · The paper itself

Abstract

backgroundCalcific aortic valve disease (CAVD) is a multifactorial condition characterized by progressive leaflet calcification with a potential role for bacterial colonization in its pathogenesis. This study investigates clinical, microbiological and molecular features of calcified versus non-calcified aortic regurgitation (AR) valves.

methodsThis is a prospective, observational study, whose primary objective was to compare the occurrence of bacterial detection between CAVD and AR. The secondary objectives included the evaluation of bone-related calcification markers in valves from CAVD and AR patients.

resultsWe analysed 31 CAVD and 8 AR valves, yielding 111 leaflets (84 calcified, 27 non-calcified). Light microscopy of CAVD leaflets revealed near-complete disruption of the three-layered valve architecture, with calcified masses extending through the leaflets, sparse cellularity and focal micro-angiogenesis; no bacteria were detected by GRAM, PAS or TEM. Enrichment culture detected low-virulence bacteria in 5.95% of CAVD and 4.16% of AR leaflets; 16S rRNA PCR was positive in 22.5% of CAVD and 12.5% of AR cases, with Staphylococcus and Streptococcus spp. predominating. Calcium content was significantly higher in CAVD leaflets (p = .001) and correlated with dyslipidemia (p = .02). Osterix expression was higher in valves with positive microbiological findings (p < .0001), while ALP was increased in CAVD and bicuspid valves regardless of microbial status. Valve interstitial cells from CAVD exhibited spontaneous in vitro calcification, unlike controls.

conclusionThe early osteogenic marker osterix was found to be upregulated in patients whose valves tested positive for microbial DNA, suggesting a potential role for bacteria in driving cellular differentiation towards an osteoblastic phenotype in CAVD.

Indexed as

Aortic ValveAortic Valve DiseaseAortic Valve InsufficiencyCalcinosisAgedAlkaline PhosphataseAortic Valve StenosisCalciumFemaleHumansMaleMiddle AgedOsteoblastsOsteocalcinProspective StudiesRNA, Ribosomal, 16SAlkaline PhosphataseCalciumOsteocalcinRNA, Ribosomal, 16SSP7 protein, humanSp7 Transcription Factorcalcific aortic valve diseaseosteoblastosterixstaphylococcus spp.streptococcus spp.VIC

Identifiers

PMID41795218
PMCPMC12967713

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.