Evidence map›Paper›PMID 31038597›Full record

ArticleArchives of endocrinology and metabolism

Paraoxonase 1 serum activity in women: the effects of menopause, the C(-107)T polymorphism and food intake.

Mauren Castro Ritta, Aline Marques Baldez, Isabel Oliveira de Oliveira, Driele Neske Garcia, Paola Spiering Souza, Kelvin Ruan da Silva Andrade, Sandra Costa Valle, Simone Pieniz, Carlos Castilho Barros, Michal M Masternak and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Archives of endocrinology and metabolism. 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
0.5field-weighted citation impact, top 37% 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. Article
  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 3 countries.

Mauren Castro RittaFaculdade de Nutrição, Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brasil.
Aline Marques BaldezFaculdade de Nutrição, Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brasil.
Isabel Oliveira de OliveiraInstituto de Biologia, Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brasil.
Driele Neske GarciaFaculdade de Nutrição, Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brasil.
Paola Spiering SouzaFaculdade de Nutrição, Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brasil.
Kelvin Ruan da Silva AndradeFaculdade de Nutrição, Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brasil.
Sandra Costa ValleFaculdade de Nutrição, Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brasil.
Simone PienizFaculdade de Nutrição, Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brasil.
Carlos Castilho BarrosFaculdade de Nutrição, Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brasil.
Michal M MasternakCollege of Medicine, Burnett School of Biomedical Sciences, University of Central Florida, Orlando, FL, USA.
Augusto SchneiderFaculdade de Nutrição, Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brasil.
Universidade Federal de Pelotas · BRUniversity of Central Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aims of this study were to investigate changes in serum paraoxonase 1 (PON1) activity in women at the pre and postmenopausal stages and its association with the PON1 C(-107)T polymorphism and food intake profile. SUBJECTS AND

methodsA cross-sectional study with female patients aged between 35 and 59 years old was conducted. Women were divided into two groups: premenopausal (n = 40) and postmenopausal (n = 36). Women enrolled in the study had serum PON1, total cholesterol, HDL, LDL, glucose and HbA1c, as well as the BMI measured. Additionally, women were genotyped for the PON1 T(-107)C polymorphism and the food intake profile was obtained through interview.

resultsGlucose (p = 0.03), HbA1c (p = 0.002) and total cholesterol (p = 0.002)concentrations were higher in post than premenopausal women, however PON1 activity was not different (p > 0.05). Carriers of the C allele had higher PON1 activity (CC: 88.9 ± 6.5 U/mL and CT: 79.9 ± 4.7 U/mL) than women of the TT genotype (66.6 ± 5.9 U/mL) (p < 0.05). However, the model predicting PON1 activity was slightly better when genotype, total fat and cholesterol content in the diet were all included.

conclusionIn sum, we observed that the PON1 C(-107)T genotype was the major regulator of PON1 activity, and menopause had no effect on PON1 activity. The lipid and glycemic profile were altered in postmenopausal women.

Indexed as

EatingAdultAryldialkylphosphataseCross-Sectional StudiesFemaleGenotypeHumansPolymorphism, GeneticPostmenopausePremenopauseAryldialkylphosphatasePON1 protein, human

Identifiers

PMID31038597
PMCPMC10522199
OpenAlexW2943822256

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.