Evidence map›Paper›PMID 32152781›Full record

ReviewReviews in endocrine & metabolic disorders2020

Serotonin pathway in carcinoid syndrome: Clinical, diagnostic, prognostic and therapeutic implications.

Giuseppe Fanciulli, Rosaria M Ruggeri, Erika Grossrubatscher, Fabio Lo Calzo, Troy D Wood, Antongiulio Faggiano, Andrea Isidori, Annamaria Colao, NIKE

Abstract readReview
PubMed Publisher
In one paragraph

Review in Reviews in endocrine & metabolic disorders, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Carcinoid Syndrome: Preclinical Models and Future Therapeutic Strategies.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Review
  15. Sex differences in carcinoid syndrome: A gap to be closed.Reviews in endocrine & metabolic disorders · 2022
    Review
  16. Review
  17. Article
  18. Update in carcinoid heart disease - the heart of the matter.Reviews in endocrine & metabolic disorders · 2021
    Review
  19. Review
  20. Article
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

9 authors at 6 institutions in 2 countries.

Giuseppe FanciulliDepartment of Medical, Surgical and Experimental Sciences, University of Sassari - Endocrine Unit, AOU Sassari, Sassari, Italy.
Rosaria M RuggeriDepartment of Clinical and Experimental Medicine, Unit of Endocrinology, University of Messina, Messina, Italy.
Erika GrossrubatscherS.C. Endocrinologia, ASST Grande Ospedale Metropolitano, Niguarda, Milan, Italy.
Fabio Lo CalzoDepartment of Clinical Medicine and Surgery, Endocrinology Unit, University Federico II, Naples, Italy.
Troy D WoodDepartment of Chemistry, University at Buffalo, Buffalo, NY, USA.
Antongiulio FaggianoDepartment of Experimental Medicine, Sapienza University of Rome, Rome, Italy. antongiulio.faggiano@uniroma1.it.
Andrea IsidoriDepartment of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
Annamaria ColaoDepartment of Clinical Medicine and Surgery, Endocrinology Unit, University Federico II, Naples, Italy.
NIKE
Federico II University Hospital · ITUniversity of Messina · ITAzienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda · ITSapienza University of Rome · ITUniversity at Buffalo, State University of New York · USUniversity of Sassari · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carcinoid syndrome represents the most common functional syndrome that affects patients with neuroendocrine neoplasms. Its clinical presentation is really heterogeneous, ranging from mild and often misdiagnosed symptoms to severe manifestations, that significantly worsen the patient's quality of life, such as difficult-to-control diarrhoea and fibrotic complications. Serotonin pathway alteration plays a central role in the pathophysiology of carcinoid syndrome, accounting for most clinical manifestations and providing diagnostic tools. Serotonin pathway is complex, resulting in production of biologically active molecules such as serotonin and melatonin, as well as of different intermediate molecules and final metabolites. These activities require site- and tissue-specific catalytic enzymes. Variable expression and activities of these enzymes result in different clinical pictures, according to primary site of origin of the tumour. At the same time, the biochemical diagnosis of carcinoid syndrome could be difficult even in case of typical symptoms. Therefore, the accuracy of the diagnostic methods of assessment should be improved, also attenuating the impact of confounding factors and maybe considering new serotonin precursors or metabolites as diagnostic markers. Finally, the prognostic role of serotonin markers has been only evaluated for its metabolite 5-hydroxyindole acetic acid but, due to heterogeneous and biased study designs, no definitive conclusions have been achieved. The most recent progress is represented by the new therapeutic agent telotristat, an inhibitor of the enzyme tryptophan hydroxylase, which blocks the conversion of tryptophan in 5-hydroxy-tryptophan. The present review investigates the clinical significance of serotonin pathway in carcinoid syndrome, considering its role in the pathogenesis, diagnosis, prognosis and therapy.

Indexed as

Signal TransductionHumansMalignant Carcinoid SyndromePhenylalaninePyrimidinesSerotoninTryptophan HydroxylasePhenylalaninePyrimidinesSerotonintelotristatTryptophan HydroxylaseAnalytical methodsCarcinoid syndromeNeuroendocrine neoplasmSerotonin pathwayTelotristat

Identifiers

PMID32152781
OpenAlexW3011793537

What OpenQuestion holds

Textmetadata
Read underepoch 390

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 OpenQuestion graph.