Evidence map›Paper›PMID 35625964›Full record

ArticleCancers2022

Elevated Serotonin and NT-proBNP Levels Predict and Detect Carcinoid Heart Disease in a Large Validation Study.

Sonja Levy, Aoife B Kilgallen, Catharina M Korse, Marish I F J Oerlemans, Joost P G Sluijter, Linda W van Laake, Gerlof D Valk, Margot E T Tesselaar

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Observational
  3. Article
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  5. Review
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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

8 authors at 3 institutions in 1 country.

Sonja LevyDepartment of Medical Oncology, Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.
Aoife B KilgallenRegenerative Medicine Centre Utrecht, Circulatory Health Laboratory, University Medical Centre Utrecht, 3584 CX Utrecht, The Netherlands.ORCID 0000-0003-4274-2427
Catharina M KorseDepartment of Laboratory Medicine, Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.
Marish I F J OerlemansDivision of Heart and Lungs, Department of Cardiology, Experimental Cardiology Laboratory, University Medical Centre Utrecht, 3584 CX Utrecht, The Netherlands.ORCID 0000-0003-3166-518X
Joost P G SluijterRegenerative Medicine Centre Utrecht, Circulatory Health Laboratory, University Medical Centre Utrecht, 3584 CX Utrecht, The Netherlands.ORCID 0000-0003-2088-9102
Linda W van LaakeRegenerative Medicine Centre Utrecht, Circulatory Health Laboratory, University Medical Centre Utrecht, 3584 CX Utrecht, The Netherlands.
Gerlof D ValkDepartment of Endocrine Oncology, University Medical Centre Utrecht, 3584 CX Utrecht, The Netherlands.
Margot E T TesselaarDepartment of Medical Oncology, Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.
University Medical Center Utrecht · NLThe Netherlands Cancer Institute · NLUtrecht University · NL

Funding

EU's H2020 research and innovation programme under Marie S. Curie cofund RESCUE 801540
6 · The paper itself

Abstract

Carcinoid heart disease (CHD) is a rare fibrotic cardiac complication of neuroendocrine tumors. Besides known biomarkers N-Terminal pro-B-type natriuretic peptide (NT-proBNP) and serotonin, activin A, connective tissue growth factor (CTGF), and soluble suppression of tumorigenicity 2 (sST2) have been suggested as potential biomarkers for CHD. Here, we validated the predictive/diagnostic value of these biomarkers in a case-control study of 114 patients between 1990 and 2021. Two time-points were analyzed: T0: liver metastasis without CHD for all patients. T1: confirmed CHD in cases (CHD+, n = 57); confirmed absence of CHD five or more years after liver metastasis in controls (CHD−, n = 57). Thirty-one (54%) and 25 (44%) females were included in CHD+ and CHD− patients, respectively. Median age was 57.9 years for CHD+ and 59.7 for CHD- patients (p = 0.290). At T0: activin A was similar across both groups (p = 0.724); NT-proBNP was higher in CHD+ patients (17 vs. 6 pmol/L, p = 0.016), area under the curve (AUC) 0.84, and the most optimal cut-off at 6.5 pmol/L. At T1: activin A was higher in CHD+ patients (0.65 vs. 0.38 ng/mL, p = 0.045), AUC 0.62, without an optimal cut-off value. NT-pro-BNP was higher in CHD+ patients (63 vs. 11 pmol/L, p < 0.001), AUC 0.89, with an optimal cut-off of 27 pmol/L. Serotonin (p = 0.345), sST2 (p = 0.867) and CTGF (p = 0.232) levels were similar across groups. This large validation study identified NT-proBNP as the superior biomarker for CHD. Patients with elevated serotonin levels and NT-proBNP levels between 6.5 and 27 pmol/L, and specifically >27 pmol/L, should be monitored closely for the development of CHD.

Indexed as

carcinoid heart diseaseNT-proBNPserotonin

Identifiers

PMID35625964
PMCPMC9139809
OpenAlexW4280509317

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.