Evidence map›Paper›PMID 37378756›Full record

Observational studyJournal of neurology2023

Retrospective observational study on the use of acetyl-L-carnitine in ALS.

Serena Sassi, Elisa Bianchi, Luca Diamanti, Danilo Tornabene, Elisabetta Sette, Doriana Medici, Sabrina Matà, Deborah Leccese, Martina Sperti, Ilaria Martinelli and 24 more

Erratum issuedOpen access · hybridAbstract readObservational Study
In one paragraph

Observational study in Journal of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

34 authors at 14 institutions in 1 country.

Serena Sassi *Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Elisa Bianchi *Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Luca DiamantiNeuro-Oncology Unit, IRCCS Mondino Foundation, Pavia, Italy.
Danilo TornabeneNeuro-Oncology Unit, IRCCS Mondino Foundation, Pavia, Italy.
Elisabetta SetteUO di Neurologia Dipartimento Neuroscienze e Riabilitazione, Azienda Ospedaliera Universitaria di Ferrara, Ferrara, Italy.
Doriana MediciPresidio Ospedaliero Fidenza AUSL Parma, Fidenza, Italy.
Sabrina MatàDipartimento Neuromuscoloscheletrico e Degli Organi di Senso, Azienda Ospedaliero-Universitaria di Careggi, Florence, Italy.
Deborah LecceseDipartimento Neuromuscoloscheletrico e Degli Organi di Senso, Azienda Ospedaliero-Universitaria di Careggi, Florence, Italy.
Martina SpertiDipartimento Neuromuscoloscheletrico e Degli Organi di Senso, Azienda Ospedaliero-Universitaria di Careggi, Florence, Italy.
Ilaria MartinelliDepartment of Neurosciences, Azienda Ospedaliero Universitaria di Modena, Modena, Italy.
Andrea GhezziDepartment of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Jessica MandrioliDepartment of Neurosciences, Azienda Ospedaliero Universitaria di Modena, Modena, Italy.
Valentina Virginia IuzzolinoDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples Federico II, Naples, Italy.
Raffaele DubbiosoDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples Federico II, Naples, Italy.
Francesca TrojsiDipartimento di Scienze Mediche e Chirurgiche Avanzate, Università degli Studi della Campania "Luigi Vanvitelli", P.Zza Miraglia 2, Naples, Italy.
Carla PassanitiDipartimento di Scienze Mediche e Chirurgiche Avanzate, Università degli Studi della Campania "Luigi Vanvitelli", P.Zza Miraglia 2, Naples, Italy.
Giulia D'AlvanoDipartimento di Scienze Mediche e Chirurgiche Avanzate, Università degli Studi della Campania "Luigi Vanvitelli", P.Zza Miraglia 2, Naples, Italy.
Massimiliano FilostoDepartment of Clinical and Experimental Sciences, NeMO-Brescia Clinical Center for Neuromuscular Diseases, University of Brescia, Brescia, Italy.
Alessandro PadovaniDepartment of Clinical and Experimental Sciences, Unit of Neurology ASST Spedali Civili Di Brescia, University of Brescia, Brescia, Italy.
Letizia MazziniALS Center Azienda Ospedaliero Universitaria "Maggiore della Carità" e Università del Piemonte Orientale, Novara, Italy.
Fabiola De MarchiALS Center Azienda Ospedaliero Universitaria "Maggiore della Carità" e Università del Piemonte Orientale, Novara, Italy.
Lucia ZinnoDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Andi NurediniDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Paolo BongioanniDpt. Medical Specialties, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.
Cristina DolciottiDpt. Medical Specialties, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.
Elena CanaliU.O di Neurologia, Presidio Ospedaliero S.Maria Nuova Azienda USL, IRCCS di Reggio Emilia, Florence, Italy.
Giulia ToschiU.O di Neurologia, Presidio Ospedaliero S.Maria Nuova Azienda USL, IRCCS di Reggio Emilia, Florence, Italy.
Antonio PetrucciCenter for Neuromuscular and Neurological Rare Diseases, San Camillo Forlanini Hospital, Rome, Italy.
Alessia PernaCenter for Neuromuscular and Neurological Rare Diseases, San Camillo Forlanini Hospital, Rome, Italy.
Vittorio RisoCenter for Neuromuscular and Neurological Rare Diseases, San Camillo Forlanini Hospital, Rome, Italy.
Maurizio InghilleriDipartimento di Neuroscienze Umane, Università di Roma "Sapienza" UOSD Malattie Neurodegenerative-Centro Malattie Rare Neuromuscolari, Policlinico Universitario Umberto I, Rome, Italy.
Laura LibonatiDipartimento di Neuroscienze Umane, Università di Roma "Sapienza" UOSD Malattie Neurodegenerative-Centro Malattie Rare Neuromuscolari, Policlinico Universitario Umberto I, Rome, Italy. laura.libonati@uniroma1.it.ORCID http://orcid.org/0000-0002-4323-3598
Chiara CambieriDipartimento di Neuroscienze Umane, Università di Roma "Sapienza" UOSD Malattie Neurodegenerative-Centro Malattie Rare Neuromuscolari, Policlinico Universitario Umberto I, Rome, Italy.
Elisabetta PupilloIstituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Azienda Ospedaliero-Universitaria Careggi · ITCarlo Forlanini Hospital · ITMario Negri Institute for Pharmacological Research · ITPoliclinico Umberto I · ITPresidio Ospedaliero · ITUniversity of Campania "Luigi Vanvitelli" · ITUniversity of Modena and Reggio Emilia · ITAzienda Ospedaliera Universitaria Pisana · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITUniversity of Brescia · ITUniversity of Naples Federico II · ITUniversity of Parma · ITArcispedale Sant'Anna · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ALCAR (Acetyl-L-carnitine) is a donor of acetyl groups and increases the intracellular levels of carnitine, the primary transporter of fatty acids across the mitochondrial membranes. In vivo studies showed that ALCAR decrease oxidative stress markers and pro-inflammatory cytokines. In a previous double-blind placebo-controlled phase II trial showed positive effects on self-sufficiency (defined as a score of 3+ on the ALSFRS-R items for swallowing, cutting food and handling utensils, and walking) ALSFRS-R total score and FVC. We conducted an observational, retrospective, multicentre, case-control study to provide additional data on the effects of ALCAR in subjects with ALS in Italy. Subjects treated with ALCAR 1.5 g/day or 3 g/day were included and matched with not treated subjects by sex, age at diagnosis, site of onset, and time from diagnosis to baseline, (45 subjects per group). ALCAR 3 g/day vs not treated: 22 not treated subjects (48.9%) were still alive at 24 months after baseline, compared to 23 (51.1%) treated subjects (adj. OR 1.18, 95% CI 0.46-3.02). No statistically significant differences were detected in ALSFRS nor FVC nor self-sufficiency. ALCAR 1.5 g/day vs not treated: 22 not treated subjects (48.9%) were still alive at 24 months after baseline, compared to 32 (71.1%) treated subjects (adj. OR 0.27, 95% CI 0.10-0.71). For ALSFRS-R, a mean slope of - 1.0 was observed in treated subjects compared to - 1.4 in those not treated (p = 0.0575). No statistically significant difference was detected in the FVC nor self-sufficiency. Additional evidence should be provided to confirm the efficacy of the drug and provide a rationale for the dosage.

Indexed as

AcetylcarnitineAmyotrophic Lateral SclerosisCase-Control StudiesDouble-Blind MethodHumansRetrospective StudiesAcetylcarnitineAmyotrophic lateral sclerosisCase–controlEfficacyNeurological diseaseObservational studyTreatment

Identifiers

PMID37378756
PMCPMC10576701
OpenAlexW4382344234

What OpenQuestion holds

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Registered trials

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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.