Evidence map›Paper›PMID 40778682›Full record

ArticleJournal of hypertension2026

Potential role of the spleen in the development of arterial hypertension in humans.

Matteo Nardin, Claudia Agabiti Rosei, Claudia Rossini, Fabio Bertacchini, Silvia Piantoni, Valeria Brami, Giulia Chiarini, Paolo Malerba, Niccolò Piacentini, Samantha Sartori and 10 more

Abstract read
In one paragraph

Article in Journal of hypertension, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Matteo NardinDivision of Internal Medicine, Department of Medicine, ASST Spedali Civili di Brescia.
Claudia Agabiti RoseiDivision of Internal Medicine, Department of Clinical and Experimental Sciences, ASST Spedali Civili Brescia, University of Brescia.
Claudia RossiniDivision of Internal Medicine, Department of Clinical and Experimental Sciences, ASST Spedali Civili Brescia, University of Brescia.
Fabio BertacchiniEmergency Medicine, Department of Medicine, ASST Spedali Civili di Brescia.
Silvia PiantoniRheumatology and Clinical Immunology Unit, Department of Clinical and Experimental Sciences, ASST Spedali Civili and University of Brescia, Brescia, Italy.
Valeria BramiDivision of Internal Medicine, Department of Clinical and Experimental Sciences, ASST Spedali Civili Brescia, University of Brescia.
Giulia ChiariniDivision of Internal Medicine, Department of Clinical and Experimental Sciences, ASST Spedali Civili Brescia, University of Brescia.
Paolo MalerbaDivision of Internal Medicine, Department of Clinical and Experimental Sciences, ASST Spedali Civili Brescia, University of Brescia.
Niccolò PiacentiniDivision of Internal Medicine, Department of Clinical and Experimental Sciences, ASST Spedali Civili Brescia, University of Brescia.
Samantha SartoriThe Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Silvia MinistriniSurgical Clinic, Department of Clinical and Experimental Sciences, University of Brescia, Brescia and ASST Spedali Civili di Brescia.
Antonella AnastasiaHematology Division, Department of Oncology, ASST Spedali Civili di Brescia.
Mariella D'AddaHematology Division, Department of Oncology, ASST Spedali Civili di Brescia.
Enzo PorteriDivision of Internal Medicine, Department of Clinical and Experimental Sciences, ASST Spedali Civili Brescia, University of Brescia.
Paolo AiròRheumatology and Clinical Immunology Unit, Department of Clinical and Experimental Sciences, ASST Spedali Civili and University of Brescia, Brescia, Italy.
Guido Alberto Massimo TiberioSurgical Clinic, Department of Clinical and Experimental Sciences, University of Brescia, Brescia and ASST Spedali Civili di Brescia.
Giuseppe RossiHematology Division, Department of Oncology, ASST Spedali Civili di Brescia.
Franco FranceschiniRheumatology and Clinical Immunology Unit, Department of Clinical and Experimental Sciences, ASST Spedali Civili and University of Brescia, Brescia, Italy.
Damiano RizzoniDivision of Internal Medicine, Department of Clinical and Experimental Sciences, ASST Spedali Civili Brescia, University of Brescia.
Carolina De CiuceisDivision of Internal Medicine, Department of Clinical and Experimental Sciences, ASST Spedali Civili Brescia, University of Brescia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesImmunity, particularly T lymphocytes, plays an important role in the development of arterial hypertension. Moreover, the so-called neuro-immune axis has been identified as a crucial crossroads, occurring in the spleen and involving placental growth factor as the principal mediator. However, no studies in humans have yet investigated the role of the spleen in hypertension and vascular damage.

methodsIn this retrospective, case-control, single-blind study, we enrolled patients who had previously undergone elective splenectomy (cases) and subjects who had undergone elective cholecystectomy (controls). All subjects underwent 24-h ambulatory blood pressure monitoring, evaluation of retinal arteriole morphology by adaptive optics, capillary density assessment by video-capillaroscopy, arterial stiffness measurements, and analysis of T lymphocyte subpopulations by flow cytometry.

resultsFifty patients were included: 25 (50%) cases and 25 (50%) controls. No difference in hypertension prevalence ( P  = 0.39) or cumulative incidence ( P  = 0.79) of new diagnoses was detected. Splenectomized patients displayed lower 24-h ( P  = 0.024) and daytime ( P  = 0.011) diastolic blood pressure compared to cholecystectomized patients. Similar results were obtained for retinal structural parameters, capillary density, and arterial stiffness between the groups. A significant impact of splenectomy on the relationship between 24-h diastolic BP and wall cross-sectional area ( P -interaction = 0.019) and forearm capillary density recruitment ( P -interaction = 0.020) was found. A higher number and percentage of CD3 + CD8 + T cells were observed in splenectomized patients compared to cholecystectomized patients ( P  = 0.009 and P  = 0.001, respectively), although no differences in cytokine production patterns were detected.

conclusionsFor the first time, our results support the role of the spleen in blood pressure control in humans. Further and larger studies are required to appropriately translate our findings into clinical practice.

Indexed as

HypertensionSpleenAdultAgedBlood Pressure Monitoring, AmbulatoryCase-Control StudiesFemaleHumansMaleMiddle AgedRetrospective StudiesSingle-Blind MethodSplenectomyVascular Stiffnesshumanshypertensionlymphocytesspleenwall to lumen ratio

Identifiers

PMID40778682
PMCPMC12672046

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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 OpenQuestion graph.