Evidence map›Paper›PMID 26362198›Full record

Observational studyJournal of translational medicine2015

Downregulation of PHEX in multibacillary leprosy patients: observational cross-sectional study.

Sandra R Boiça Silva, Ximena Illarramendi, Antonio J Tempone, Pedro H L Silva, José A C Nery, Alexandra M V Monteiro, Maria Cristina V Pessolani, Edson Boasquevisque, Euzenir N Sarno, Geraldo M B Pereira and 1 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Journal of translational medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact, top 92% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
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

11 authors at 2 institutions in 1 country.

Sandra R Boiça SilvaDisciplina de Patologia Geral e Laboratório de Imunopatologia, Departamento de Patologia e Laboratórios, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro (UERJ), Av Professor Manuel de Abreu 444, Vila Isabel, Rio de Janeiro, RJ, 20550-170, Brazil. sandraboica@gmail.com.
Ximena IllarramendiLaboratório de Hanseníase, Instituto Oswaldo Cruz (IOC) - Oswaldo Cruz Foundation (FIOCRUZ), Av. Brasil 4365, Manguinhos, Rio de Janeiro, RJ, 21040-360, Brazil. anemirx@gmail.com.
Antonio J TemponeLaboratório de Biologia Molecular de Parasitas e Vetores, Instituto Oswaldo Cruz (IOC) - Oswaldo Cruz Foundation (FIOCRUZ), Av. Brasil 4365, Manguinhos, Rio de Janeiro, RJ, 21040-360, Brazil. tempone@ioc.fiocruz.br.
Pedro H L SilvaLaboratório de Hanseníase, Instituto Oswaldo Cruz (IOC) - Oswaldo Cruz Foundation (FIOCRUZ), Av. Brasil 4365, Manguinhos, Rio de Janeiro, RJ, 21040-360, Brazil. peddro.henrique@gmail.com.
José A C NeryLaboratório de Hanseníase, Instituto Oswaldo Cruz (IOC) - Oswaldo Cruz Foundation (FIOCRUZ), Av. Brasil 4365, Manguinhos, Rio de Janeiro, RJ, 21040-360, Brazil. neryjac@ioc.fiocruz.br.
Alexandra M V MonteiroServiço de Medicina Nuclear, Departamento de Radiologia, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro (UERJ), Av. Prof. Manuel de Abreu 444, Vila Isabel, Rio de Janeiro, RJ, 20550-170, Brazil. monteiroamv@gmail.com.
Maria Cristina V PessolaniLaboratório de Microbiologia Celular, Instituto Oswaldo Cruz (IOC) - Oswaldo Cruz Foundation (FIOCRUZ), Av. Brasil 4365, Manguinhos, Rio de Janeiro, RJ, 21040-360, Brazil. cpessola@ioc.fiocruz.br.
Edson BoasquevisqueServiço de Medicina Nuclear, Departamento de Radiologia, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro (UERJ), Av. Prof. Manuel de Abreu 444, Vila Isabel, Rio de Janeiro, RJ, 20550-170, Brazil. boasquevisque@gmail.com.
Euzenir N SarnoLaboratório de Hanseníase, Instituto Oswaldo Cruz (IOC) - Oswaldo Cruz Foundation (FIOCRUZ), Av. Brasil 4365, Manguinhos, Rio de Janeiro, RJ, 21040-360, Brazil. euzenir@ioc.fiocruz.br.
Geraldo M B PereiraLaboratório de Microbiologia Celular, Instituto Oswaldo Cruz (IOC) - Oswaldo Cruz Foundation (FIOCRUZ), Av. Brasil 4365, Manguinhos, Rio de Janeiro, RJ, 21040-360, Brazil. gmbpereira@gmail.com.
Danuza EsquenaziLaboratório de Hanseníase, Instituto Oswaldo Cruz (IOC) - Oswaldo Cruz Foundation (FIOCRUZ), Av. Brasil 4365, Manguinhos, Rio de Janeiro, RJ, 21040-360, Brazil. esquenazi.danuza@gmail.com.
Fundação Oswaldo Cruz · BRUniversidade do Estado do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeripheral nerve injury and bone lesions, well known leprosy complications, lead to deformities and incapacities. The phosphate-regulating gene with homologies to endopeptidase on the X chromosome (PHEX) encodes a homonymous protein (PHEX) implicated in bone metabolism. PHEX/PHEX alterations may result in bone and cartilage lesions. PHEX expression is downregulated by intracellular Mycobacterium leprae (M. leprae) in cultures of human Schwann cells and osteoblasts. M. leprae in vivo effect on PHEX/PHEX is not known.

methodsCross-sectional observational study of 36 leprosy patients (22 lepromatous and 14 borderline-tuberculoid) and 20 healthy volunteers (HV). The following tests were performed: PHEX flow cytometric analysis on blood mononuclear cells, cytokine production in culture supernatant, 25-hydroxyvitamin D (OHvitD) serum levels and (99m)Tc-MDP three-phase bone scintigraphy, radiography of upper and lower extremities and blood and urine biochemistry.

resultsSignificantly lower PHEX expression levels were observed in lepromatous patients than in the other groups (χ(2) = 16.554, p < 0.001 for lymphocytes and χ(2) = 13.933, p = 0.001 for monocytes). Low levels of 25-(OHvitD) were observed in HV (median = 23.0 ng/mL) and BT patients (median = 27.5 ng/mL) and normal serum levels were found in LL patients (median = 38.6 ng/mL). Inflammatory cytokines, such as TNF, a PHEX transcription repressor, were lower after stimulation with M. leprae in peripheral blood mononuclear cells from lepromatous in comparison to BT patients and HV (χ(2) = 10.820, p < 0.001).

conclusionDownregulation of PHEX may constitute an important early component of bone loss and joint damage in leprosy. The present results suggest a direct effect produced by M. leprae on the osteoarticular system that may use this mechanism.

Indexed as

Down-RegulationAdolescentAdultAgedAged, 80 and overBone and BonesCartilageCross-Sectional StudiesCytokinesFemaleFlow CytometryHealthy VolunteersHumansInflammationLeprosy, BorderlineLeprosy, MultibacillaryCytokinesPHEX Phosphate Regulating Neutral EndopeptidasePHEX protein, humanTechnetium Tc 99m Medronate

Identifiers

PMID26362198
PMCPMC4566286
OpenAlexW2168910453

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.