Evidence map›Paper›PMID 40138010›Full record

SynthesisCerebellum (London, England)2025

Epidemiology of Autosomal Dominant Spinocerebellar Ataxias in Latin America: A Systematic Review and Meta-Analysis.

Milagros Galecio-Castillo, Jesus Gutierrez-Arratia, Alonso Abad-Murillo, Elison Sarapura-Castro, Ismael Araujo-Aliaga, Ana Saldarriaga-Mayo, Maryenela Illanes-Manrique, Mario Cornejo-Olivas

Abstract readSystematic ReviewMeta-Analysis
PubMed Publisher
In one paragraph

Synthesis in Cerebellum (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
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.

Milagros Galecio-CastilloNeurogenetics Working Group, Universidad Cientifica del Sur, Carretera Panamericana Sur Km. 19, Villa El Salvador, Lima, Perú.ORCID http://orcid.org/0000-0002-8107-9632
Jesus Gutierrez-ArratiaNeurogenetics Research Center, Instituto Nacional de Ciencias Neurológicas, Lima, Peru.ORCID http://orcid.org/0000-0003-4082-5966
Alonso Abad-MurilloNeurogenetics Working Group, Universidad Cientifica del Sur, Carretera Panamericana Sur Km. 19, Villa El Salvador, Lima, Perú.ORCID http://orcid.org/0000-0001-8552-8792
Elison Sarapura-CastroNeurogenetics Working Group, Universidad Cientifica del Sur, Carretera Panamericana Sur Km. 19, Villa El Salvador, Lima, Perú.ORCID http://orcid.org/0000-0002-1562-3062
Ismael Araujo-AliagaNeurogenetics Working Group, Universidad Cientifica del Sur, Carretera Panamericana Sur Km. 19, Villa El Salvador, Lima, Perú.ORCID http://orcid.org/0000-0002-8661-9351
Ana Saldarriaga-MayoNeurogenetics Working Group, Universidad Cientifica del Sur, Carretera Panamericana Sur Km. 19, Villa El Salvador, Lima, Perú.ORCID http://orcid.org/0000-0002-1150-6715
Maryenela Illanes-ManriqueNeurogenetics Working Group, Universidad Cientifica del Sur, Carretera Panamericana Sur Km. 19, Villa El Salvador, Lima, Perú.ORCID http://orcid.org/0000-0002-3098-0981
Mario Cornejo-OlivasNeurogenetics Working Group, Universidad Cientifica del Sur, Carretera Panamericana Sur Km. 19, Villa El Salvador, Lima, Perú. mcornejool@cientifica.edu.pe.ORCID http://orcid.org/0000-0001-6313-5680

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Spinocerebellar Ataxias (SCAs) are a group of autosomal dominant neurodegenerative disorders characterized by progressive cerebellar ataxia, affecting motor coordination. SCAs are reported globally with large geographical and ethnic differences. This systematic review and meta-analysis aimed to update the frequency, and geographic distribution of SCAs in Latin America, including recently identified SCAs like SCA27B. We conducted a systematic search in PubMed, Scopus, LILACS, SciELO, and Web of Science databases, including studies published from inception to January 2025. We included 27 studies for the systematic review and 18 studies for the meta-analysis that met the inclusion criteria, representing a total of 5859 participants across eleven countries. Our meta-analysis revealed that about 50% (95% CI 26-74%) of hereditary ataxias in Latin America were confirmed to have a genetic diagnosis of SCA. The included participants with a known SCA have the following proportions: MJD/SCA3 (15%), SCA2 (11%), SCA7 (4%), SCA10 (3%), and SCA1 (3%). Geographic distributions were notable, MJD/SCA3 in Brazil, SCA2 in Cuba, Argentina and Mexico, SCA10 predominating in Peru, and SCA7 in Venezuela. Recently identified SCA types, like SCA27B and one case of SCA4, were identified in Brazil. In 22 countries there are no published studies on the epidemiology of SCAs. The distribution of SCAs in Latin America reflects the influence of historical migrations, founder effects, and ancestries, emphasizing regional heterogeneity. Our findings underscore the critical need for further epidemiological studies, particularly in understudied countries in the region.

Indexed as

Spinocerebellar AtaxiasHumansLatin AmericaEpidemiologyLatin AmericaMeta-analysisSCASpinocerebellar ataxiaSystematic review

Identifiers

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.