Evidence map›Paper›PMID 19911314›Full record

ArticleNeuromolecular medicine2010

Kinesin light chain 1 gene haplotypes in three conformational diseases.

Malin von Otter, Sara Landgren, Staffan Nilsson, Caroline Lundvall, Lennart Minthon, Nenad Bogdanovic, Niels Andreasen, Deborah R Gustafson, Ingmar Skoog, Anders Wallin and 6 more

Abstract read
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In one paragraph

Article in Neuromolecular medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. A novel ARC gene polymorphism is associated with reduced risk of Alzheimer's disease.Journal of neural transmission (Vienna, Austria : 1996) · 2012
    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

16 authors at 5 institutions in 2 countries.

Malin von OtterDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden. malin.vonotter@gu.se
Sara Landgren
Staffan Nilsson
Caroline Lundvall
Lennart Minthon
Nenad Bogdanovic
Niels Andreasen
Deborah R Gustafson
Ingmar Skoog
Anders Wallin
Anna Håkansson
Hans Nissbrandt
Madeleine Zetterberg
Gunnar Tasa
Kaj Blennow
Henrik Zetterberg
University of Gothenburg · SEKarolinska Institutet · SEChalmers University of Technology · SELund University · SEUniversity of Tartu · EE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A functional intracellular transport system is essential to maintain cell shape and function especially in elongated cells, e.g. neurons and lens fibre cells. Impaired intracellular transport has been suggested as a common pathological mechanism for age-related diseases characterised by protein aggregation. Here, we hypothesise that common genetic variation in the transport protein kinesin may influence the risk of Parkinson's disease (PD), Alzheimer's disease (AD) and age-related cataract. This case-control study involves a PD material (165 cases and 190 controls), an AD material (653 cases and 845 controls) and a cataract material (495 cases and 183 controls). Genetic variation in the kinesin light chain 1-encoding gene (KLC1) was tagged by six tag single nucleotide polymorphisms (SNPs). Single SNPs and haplotypes were analysed for associations with disease risk, age parameters, mini-mental state examination scores and cerebrospinal fluid biomarkers for AD using logistic or linear regression. Genetic variation in KLC1 did not influence risk of PD. Weak associations with risk of AD were seen for rs8007903 and rs3212079 (P (c) = 0.04 and P (c) = 0.02, respectively). Two SNPs (rs8007903 and rs8702) influenced risk of cataract (P (c) = 0.0007 and P (c) = 0.04, respectively). However, the allele of rs8007903 that caused increased risk of AD caused reduced risk of cataract, speaking against a common functional effect of this particular SNP in the two diseases. Haplotype analyses did not add significantly to the associations found in the single SNP analyses. Altogether, these results do not convincingly support KLC1 as a major susceptibility gene in any of the studied diseases, although there is a small effect of KLC1 in relation to cataract.

Indexed as

Genetic VariationHaplotypesAgedAlzheimer DiseaseCataractEstoniaFemaleGenetic Predisposition to DiseaseGenotypeHumansKinesinsMaleMicrotubule-Associated ProteinsMiddle AgedParkinson DiseasePolymorphism, Single NucleotideKinesinsKLC1 protein, humanMicrotubule-Associated Proteins

Identifiers

PMID19911314
OpenAlexW2004887168

What OpenQuestion holds

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Read underepoch 390

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.