Evidence map›Paper›PMID 28793858›Full record

ArticleBMC evolutionary biology2017

mtDNA structure: the women who formed the Brazilian Northeast.

Ana Paula Schaan, Lorenna Costa, Diego Santos, Antonio Modesto, Marcos Amador, Camile Lopes, Sílvia Helena Rabenhorst, Raquel Montenegro, Bruno D A Souza, Thayson Lopes and 4 more

RetractedAbstract readRetracted Publication
In one paragraph

Article in BMC evolutionary biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–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

14 citing papers in PubMed.

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  5. Mitochondria inInternational journal of molecular sciences · 2022
    Review
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  8. Previous vitamin D status and total cholesterol are associated with SARS-CoV-2 infection.Clinica chimica acta; international journal of clinical chemistry · 2021
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Ana Paula SchaanHuman and Medical Genetics Laboratory, Federal University of Pará, Av. Augusto Corrêa, 01 - Cidade Universitária Prof. José Silveira Netto - Guamá, Belém, PA, 66075-110, Brazil.
Lorenna CostaClinical and Toxicological Analyses Department, Federal University of Rio Grande do Norte, Natal, RN, 59300-000, Brazil.
Diego SantosClinical and Toxicological Analyses Department, Federal University of Rio Grande do Norte, Natal, RN, 59300-000, Brazil.
Antonio ModestoHuman and Medical Genetics Laboratory, Federal University of Pará, Av. Augusto Corrêa, 01 - Cidade Universitária Prof. José Silveira Netto - Guamá, Belém, PA, 66075-110, Brazil.
Marcos AmadorHuman and Medical Genetics Laboratory, Federal University of Pará, Av. Augusto Corrêa, 01 - Cidade Universitária Prof. José Silveira Netto - Guamá, Belém, PA, 66075-110, Brazil.
Camile LopesHuman and Medical Genetics Laboratory, Federal University of Pará, Av. Augusto Corrêa, 01 - Cidade Universitária Prof. José Silveira Netto - Guamá, Belém, PA, 66075-110, Brazil.
Sílvia Helena RabenhorstPathology and Legal Medicine Department, Federal University of Ceará, Fortaleza, CE, 60020-181, Brazil.
Raquel MontenegroCenter of Research and Drug Development, Federal University of Ceará, Fortaleza, CE, 60430-270, Brazil.
Bruno D A SouzaHuman and Medical Genetics Laboratory, Federal University of Pará, Av. Augusto Corrêa, 01 - Cidade Universitária Prof. José Silveira Netto - Guamá, Belém, PA, 66075-110, Brazil.
Thayson LopesGenetics and Molecular Biology Laboratory, Federal University of Piauí, Parnaíba, PI, 64202-020, Brazil.
France Keiko YoshiokaGenetics and Molecular Biology Laboratory, Federal University of Piauí, Parnaíba, PI, 64202-020, Brazil.
Giovanny PintoGenetics and Molecular Biology Laboratory, Federal University of Piauí, Parnaíba, PI, 64202-020, Brazil.
Vivian SilbigerClinical and Toxicological Analyses Department, Federal University of Rio Grande do Norte, Natal, RN, 59300-000, Brazil.
Ândrea Ribeiro-Dos-SantosHuman and Medical Genetics Laboratory, Federal University of Pará, Av. Augusto Corrêa, 01 - Cidade Universitária Prof. José Silveira Netto - Guamá, Belém, PA, 66075-110, Brazil. akelyufpa@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe distribution of mitochondrial DNA (mtDNA) lineages in Brazil is heterogeneous due to different regional colonization dynamics. Northeastern Brazil, although being an important region in terms of human imigration and ethnic admixture, has little information regarding its population mtDNA composition. Here, we determine which mitochondrial lineages contributed to the formation of the Northeastern Brazilian population. Our sample consisted of 767 individuals distributed as follows i) 550 individuals from eight Northeastern states (Piauí, Ceará, Rio Grande do Norte, Paraíba, Pernambuco, Alagoas, Sergipe, and Bahia) which were sequenced for mtDNA hypervariable segments I, II, and III; ii) 217 individuals from Alagoas and Pernambuco (previously published data). Data analysis was performed through sequence alignment and Haplogrep 2.0 haplogroup assignment tools. Furthermore, maternal ancestry distribution was contextualized and, when possible, related to historical events to better understand the biological interactions and population dynamics that occurred in this region since the beginning of colonization.

resultsUnexpectedly, Amerindian mitochondrial ancestry was the highest in the Northeastern region overall, followed by African, European and non-Amerindian Asian, unlike previous results for this region. Alagoas and Pernambuco states, however, showed a larger African mtDNA frequency. The Northeastern region showed an intraregional heterogeneous distribution regarding ancestral groups, in which states/mesoregions located to the north had a prevalent Amerindian ancestral frequency and those to the south had predominance of African ancestry. Moreover, results showed great diversity of European haplogroups and the presence of non-Amerindian Asian haplogroups.

conclusionsOur findings are in disagreement with previous investigations that suggest African mitochondrial ancestry is the most prevalent in the Brazilian Northeast. The predominance of Amerindian lineages exemplifies the importance of indigenous women in the formation of the population, despite intense African slave entry and conflicts with European settlers. The variable distribution of ancestral groups observed in the Northeast is in accordance with historical records showing the similarities with colonization dynamics occurred in the Amazon region and the Brazilian Southeast. Moreover, the variety of European haplogroups suggests multiple origins of founding groups, specially those found in Western European populations.

Indexed as

American Indian or Alaska NativeAsian PeopleBlack PeopleBrazilDNA, MitochondrialEthnicityFemaleGenetics, PopulationGenetic VariationGeographyHaplotypesHumansPhylogenyWhite PeopleDNA, MitochondrialAsymmetric colonizationGenetic diversityMigration patternmtDNA lineagesNortheastern BrazilPopulation admixture

Identifiers

PMID28793858
PMCPMC5549335

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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.