Evidence map›Paper›PMID 17605047›Full record

ArticleHuman genetics2007

A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3.

Sylvain Hanein, Alexandra Dürr, Pascale Ribai, Sylvie Forlani, Anne-Louise Leutenegger, Isabelle Nelson, Marie-Claude Babron, Nizar Elleuch, Christel Depienne, Céline Charon and 2 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Human genetics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00136630 (Natural History, Genetic Bases and Phenotype-genotype Correlations in Autosomal Dominant Spinocerebellar Degenerations), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 34% 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.

NCT00136630 completednot on this map

Natural History, Genetic Bases and Phenotype-genotype Correlations in Autosomal Dominant Spinocerebellar Degenerations

TypeobservationalSponsorInstitut National de la Santé Et de la Recherche Médicale, FranceRan2005 to 2020Enrolled175ConditionsSpinocerebellar Ataxias, Spastic Paraplegias
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 29 citations in OpenAlex.

  1. Hereditary Spastic Paraplegia: An Update.International journal of molecular sciences · 2022
    Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Recent advances in the genetics of spastic paraplegias.Current neurology and neuroscience reports · 2008
    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

12 authors at 4 institutions in 1 country.

Sylvain HaneinINSERM, Unit 679, 47 Bd de l'Hôpital, 75013 Paris, France.
Alexandra Dürr
Pascale Ribai
Sylvie Forlani
Anne-Louise Leutenegger
Isabelle Nelson
Marie-Claude Babron
Nizar Elleuch
Christel Depienne
Céline Charon
Alexis Brice
Giovanni Stevanin
Inserm · FRAssistance Publique – Hôpitaux de Paris · FRCentre National de Recherche en Génomique Humaine · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary spastic paraplegias (HSPs) are genetically and phenotypically heterogeneous. Both "uncomplicated" and "complicated" forms have been described, with autosomal dominant, autosomal recessive, and X-linked inheritance. Hitherto, ten autosomal dominant "uncomplicated" HSP (ADHSP) loci have been mapped. Here, we report linkage of ADHSP with markers of the 8p21.1-q13.3 chromosomal region in a large French family, including 29 examined at-risk individuals. The age at onset varied from 8 to 60 years with a mean of 31.6 +/- 16.4 years. Multipoint and two-point LOD-score calculations as well as haplotype reconstruction in this region gave support to the location of this novel ADHSP locus (SPG37) in a 43.5 cM genetic interval flanked by loci D8S1839 and D8S1795. The region was shared by all definitely (n = 13), probably (n = 3) and possibly (n = 2) affected patients with a maximum LOD score of 4.20 at the D8S601 locus. Two candidate genes, encoding the kinesin family member 13B and neuregulin 1 (isoforms SMDF and GFF2), were screened for mutations, but no disease-causing alterations were identified. Interestingly, another region, on chromosome 10q22.3-23.31, was found to segregate in all affected patients (but not in probably or possibly affected subjects) and in a high proportion of healthy at risk individuals, suggesting that this locus might act as a modifier of the phenotype.

Indexed as

Genes, DominantAdolescentAdultAgedAge of OnsetChildChromosome MappingChromosomes, Human, Pair 10Chromosomes, Human, Pair 8FemaleGenetic MarkersHaplotypesHumansKinesinsLod ScoreMaleGenetic MarkersKIF13B protein, humanKinesinsNerve Tissue ProteinsNeuregulin-1NRG1 protein, human

Identifiers

PMID17605047
OpenAlexW2006745236

What OpenQuestion holds

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Registered trials

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.