Evidence map›Paper›PMID 35032665›Full record

ReviewProstaglandins & other lipid mediators2022

The function of specialized pro-resolving endogenous lipid mediators, vitamins, and other micronutrients in the control of the inflammatory processes: Possible role in patients with SARS-CoV-2 related infection.

Claudio G Gallo, Sirio Fiorino, Giovanni Posabella, Donato Antonacci, Antonio Tropeano, Emanuele Pausini, Carlotta Pausini, Tommaso Guarniero, Wandong Hong, Enrico Giampieri and 7 more

Open access · greenAbstract readReview
In one paragraph

Review in Prostaglandins & other lipid mediators, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Bioactivity of Synthesized Trifluoromethyl Thioxanthone Analogues.Pharmaceuticals (Basel, Switzerland) · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Synthesis and Anti-Inflammatory Activity ofMolecules (Basel, Switzerland) · 2023
    Article
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  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
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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

17 authors at 6 institutions in 2 countries.

Claudio G GalloEmilian Physiolaser Therapy Center, Castel S. Pietro Terme, Bologna, Italy. Electronic address: galclaudio@libero.it.
Sirio FiorinoInternal Medicine Unit, Budrio Hospital Azienda USL, Bologna, Italy.
Giovanni PosabellaComune di Bologna, Bologna, Italy.
Donato AntonacciMedical Science Department, "Casa Sollievo della Sofferenza" Hospital, San Giovanni Rotondo, FG, Italy.
Antonio TropeanoComune di Bologna, Bologna, Italy.
Emanuele PausiniComune di Bologna, Bologna, Italy.
Carlotta PausiniComune di Bologna, Bologna, Italy.
Tommaso GuarnieroComune di Bologna, Bologna, Italy.
Wandong HongDepartment of Gastroenterology and Hepatology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou City, Zhejiang, People's Republic of China.
Enrico GiampieriExperimental, Diagnostic and Specialty Medicine Department, University of Bologna, Bologna, Italy.
Ivan CorazzaExperimental, Diagnostic and Specialty Medicine Department, University of Bologna, Bologna, Italy.
Rossella LoiaconoInternal Medicine Unit, Medical and Surgical Sciences Department, University of Bologna, Bologna, Italy.
Elisabetta LoggiHepatology Unit, Medical and Surgical Sciences Department, University of Bologna, Bologna, Italy.
Dario de BiaseDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.
Maddalena ZippiUnit of Gastroenterology and Digestive Endoscopy, Sandro Pertini Hospital, Rome, Italy.
Federico LariInternal Medicine Unit, Budrio Hospital Azienda USL, Bologna, Italy.
Marco ZancanaroComune di Bologna, Bologna, Italy.
University of Bologna · ITAzienda USL di Bologna · ITCasa Sollievo della Sofferenza · ITOspedale Sandro Pertini · ITPresidio Ospedaliero · ITWenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammation is an essential protective response against harmful stimuli, such as invading pathogens, damaged cells, or irritants. Physiological inflammation eliminates pathogens and promotes tissue repair and healing. Effective immune response in humans depends on a tightly regulated balance among inflammatory and anti-inflammatory mechanisms involving both innate and adaptive arms of the immune system. Excessive inflammation can become pathological and induce detrimental effects. If this process is not self-limited, an inappropriate remodeling of the tissues and organs can occur and lead to the onset of chronic degenerative diseases. A wide spectrum of infectious and non-infectious agents may activate the inflammation, via the release of mediators and cytokines by distinct subtypes of lymphocytes and macrophages. Several molecular mechanisms regulate the onset, progression, and resolution of inflammation. All these steps, even the termination of this process, are active and not passive events. In particular, a complex interplay exists between mediators (belonging to the group of Eicosanoids), which induce the beginning of inflammation, such as Prostaglandins (PGE2), Leukotrienes (LT), and thromboxane A2 (TXA2), and molecules which display a key role in counteracting this process and in promoting its proper resolution. The latter group of mediators includes: ω-6 arachidonic acid (AA)-derived metabolites, such as Lipoxins (LXs), ω -3 eicosapentaenoic acid (EPA)-derived mediators, such as E-series Resolvins (RvEs), and ω -3 docosahexaenoic (DHA)-derived mediators, such as D-series Resolvins (RvDs), Protectins (PDs) and Maresins (MaRs). Overall, these mediators are defined as specialized pro-resolving mediators (SPMs). Reduced synthesis of these molecules may lead to uncontrolled inflammation with possible harmful effects. ω-3 fatty acids are widely used in clinical practice as rather inexpensive, safe, readily available supplemental therapy. Taking advantage of this evidence, several researchers are suggesting that SPMs may have beneficial effects in the complementary treatment of patients with severe forms of SARS-CoV-2 related infection, to counteract the "cytokine storm" observed in these individuals. Well-designed and sized trials in patients suffering from COVID-19 with different degrees of severity are needed to investigate the real impact in the clinical practice of this promising therapeutic approach.

Indexed as

COVID-19SARS-CoV-2Docosahexaenoic AcidsEicosanoidsHumansInflammationInflammation MediatorsMicronutrientsVitaminsDocosahexaenoic AcidsEicosanoidsInflammation MediatorsMicronutrientsVitaminsCoV-2Covid-19Cytokine stormInflammationResolvinsSPMsω-3ω-6

Identifiers

PMID35032665
PMCPMC8752446
OpenAlexW4206191133

What Socratic 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 Socratic graph.