Evidence map›Paper›PMID 28527106›Full record

ArticleMolecular neurobiology2018

A Trans-acting Factor May Modify Age at Onset in Familial Amyloid Polyneuropathy ATTRV30M in Portugal.

Miguel Alves-Ferreira, Teresa Coelho, Diana Santos, Jorge Sequeiros, Isabel Alonso, Alda Sousa, Carolina Lemos

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

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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

7 authors at 2 institutions in 2 countries.

Miguel Alves-FerreiraUnIGENe, IBMC-Institute for Molecular and Cell Biology; Institute for Research and Innovation in Health Sciences (i3S), University of Porto, 4200-135, Porto, Portugal.
Teresa CoelhoUnidade Corino de Andrade (UCA), Centro Hospitalar do Porto (CHP), Largo Prof. Abel Salazar, 4050, Porto, Portugal.
Diana SantosUnIGENe, IBMC-Institute for Molecular and Cell Biology; Institute for Research and Innovation in Health Sciences (i3S), University of Porto, 4200-135, Porto, Portugal.
Jorge SequeirosUnIGENe, IBMC-Institute for Molecular and Cell Biology; Institute for Research and Innovation in Health Sciences (i3S), University of Porto, 4200-135, Porto, Portugal.
Isabel AlonsoUnIGENe, IBMC-Institute for Molecular and Cell Biology; Institute for Research and Innovation in Health Sciences (i3S), University of Porto, 4200-135, Porto, Portugal.
Alda SousaUnIGENe, IBMC-Institute for Molecular and Cell Biology; Institute for Research and Innovation in Health Sciences (i3S), University of Porto, 4200-135, Porto, Portugal.
Carolina LemosUnIGENe, IBMC-Institute for Molecular and Cell Biology; Institute for Research and Innovation in Health Sciences (i3S), University of Porto, 4200-135, Porto, Portugal. clclemos@ibmc.up.pt.ORCID http://orcid.org/0000-0001-9803-9584
Universidade do Porto · PTCentro Hospitalar do Porto · PT

Funding

Fundação para a Ciência e a Tecnologia PTDC/SAU-GMG/100240/2008 and PEsTFundação para a Ciência e a Tecnologia SFRH/BD/101352/2014Fundação para a Ciência e a Tecnologia SFRH/BD/91160/2012
6 · The paper itself

Abstract

Although all familial amyloid polyneuropathy (FAP) ATTRV30M patients carry the same causative mutation, early (<40) and late-onset forms (≥50 years) of FAP may coexist in the same family. However, this variability in age at onset is still unexplained. To identify modifiers closely linked to the TTR locus that may in part be associated with age at onset of FAP ATTRV30M, in particular in a group of very early-onset patients (≤30 years) when compared with late-onset individuals. A clinical genetic study at a referral center comprising a sample of 910 Portuguese individuals includes 589 Val30Met carriers, 102 spouses, and 189 controls from the general population. Haplotype analysis was performed, using eight intragenic single nucleotide polymorphisms (SNPs) at the TTR locus. We compared haplotypes frequency in FAP samples and controls and in parent-offspring pairs using appropriated statistical analysis. Haplotype A was the most common in the general population. Noteworthy, haplotype C was more frequent in early-onset (<40) than in late-onset patients (≥50 years) (p = 0.012). When comparing allelic frequencies of each SNP within haplotype C between "very early" (≤30 years) and late-onset (≥50 years) cases, the A allele of rs72922947 was associated with an earlier onset (p = 0.009); this remained significant after a permutation-based correction. Also, the heterozygous genotype (GA) for this SNP was associated with a decrease in mean age at onset of 8.6 years (p = 0.014). We found a more common haplotype (A) linked to the Val30Met variant and a possible modulatory trans effect on age at onset. These findings may lead to potential therapeutical targets.

Indexed as

HaplotypesMutationPolymorphism, Single NucleotideAdultAge of OnsetAllelesAmyloid Neuropathies, FamilialCase-Control StudiesFemaleGene FrequencyHumansMaleMiddle AgedPortugalPrealbuminPrealbuminAge at onsetFamilial amyloid polyneuropathy (FAP)HaplotypeTrans effectTransthyretin-related amyloidosisTransthyretin (TTR)

Identifiers

PMID28527106
OpenAlexW2616631419

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.