Caio Parente Barbosa

No ORCID on file · 71 papers in corpus · active 2000-2024

Study types

  • article 60
  • book-chapter 4
  • other 3
  • review 2
  • dataset 1

Condition tags

  • endometriosis 65
  • mesh:D004715 42
  • infertility 30
  • dysmenorrhea 3
  • mesh:D004414 1
  • chronic_pelvic_pain 1
  • mesh:D017699 1
  • endometrioma 1
  • dyspareunia 1
  • mesh:D004412 1
article 2024
BMC women's health ·doi:10.1186/s12905-024-03080-5

BACKGROUND: A women's chances of getting pregnant decreases in cases of infertility, which may have several clinical etiologies. The prevalence of infertility is estimated as 10-15% worldwide. One of the causes of infertility is endometrios…

other 2024
DNA and cell biology ·doi:10.1089/dna.2023.0395

Dynamic mutations in the 5' untranslated region of FMR1 are associated with infertility. Premutation alleles interfere with prenatal development and increase infertility risks. The number of CGG repeats that causes the highest decrease in o…

other 2023
Einstein (Sao Paulo, Brazil) ·doi:10.31744/einstein_journal/2023AO0483

OBJECTIVE: The follicle-stimulating hormone subunit beta gene rs10835638 variant (c.-211G>T) may have detrimental effects on fertility and protective effects against endometriosis. A case-control analysis was performed, aiming to investigat…

article 2022
Scientific reports ·doi:10.1038/s41598-022-24775-5

Infertility is a worldwide concern, affecting one in six couples throughout their reproductive period. Therefore, enhancing the clinical tools available to identify the causes of infertility may save time, money, and emotional distress for …

article 2022
Biomarkers in medicine ·doi:10.2217/bmm-2021-0076

Background: Homocysteine levels can be impacted by enzymes variations. Aim: To correlate MTHFR, MTR and MTRR variants with homocysteine levels in the blood and follicular fluid and assisted reproduction results. Material & methods: MTHFR (r…

article 2021
Frontiers in endocrinology ·doi:10.3389/fendo.2021.760616

Background Single nucleotide variants (SNVs) FSHB :c.-211G>T, FSHR :c.919G>A, and FSHR :c.2039G>A were reported to be associated with the variability in FSH and LH levels, and in vitro fertilization (IVF) outcomes. In this study, w…

article 2020

Additional file 1.

article 2020
Diagnostics ·doi:10.3390/diagnostics10080533

The etiology of endometriosis is highly complex, and although it is a benign disease, it has several biological behaviors similar to malignant lesions, including cell invasion, neo-angiogenesis, and decreased apoptosis. Survivin is a protei…

article 2020
BMC women's health ·doi:10.1186/s12905-020-00987-7

BACKGROUND: The quality of life (QoL) of patients with endometriosis and infertility was assessed in different stages and correlated with the clinical features of the cases. METHODS: The present study was a cross-sectional study; 106 women …

article 2019
Annals of human genetics ·doi:10.1111/ahg.12309

The STAT4 gene is vital to signaling pathways in the immune response. Immunological alterations are involved in the pathogenesis of endometriosis, and STAT4 polymorphisms may be linked to disease development. This study's aim is to evaluate…

article 2018
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology ·doi:10.1080/09513590.2018.1499090

A previous GWAS study performed on Brazilian pooled samples indicated some SNPs (single nucleotide polymorphisms) differentially frequent in infertile patients with endometriosis and controls. Some of them were located in the genes whose bi…

article 2018
DNA and cell biology ·doi:10.1089/dna.2017.4093

Endometriosis is an estrogen-dependent inflammatory disease that affects a large number of women in reproductive age. Follicle-stimulating hormone (FSH) plays a role in steroidogenesis and acts through a transmembrane glycoprotein, FSH rece…

review 2017
Einstein (Sao Paulo, Brazil) ·doi:10.1590/s1679-45082017rw3827

OBJECTIVE: To evaluate PTPN22 C1858T polymorphism and the risk of endometriosis. METHODS: A meta-analysis of 10 published case-control studies (from four articles), with a total sample of 971 cases and 1,181 controls, was performed. We esti…

dataset 2017
·doi:10.6084/m9.figshare.5667835

ABSTRACT Objective To evaluate PTPN22 C1858T polymorphism and the risk of endometriosis. Methods A meta-analysis of 10 published case-control studies (from four articles), with a total sample of 971 cases and 1,181 controls, was performed. …

article 2017
·doi:10.1016/j.fertnstert.2017.07.599
article 2017
·doi:10.5301/jeppd.5000294

Introduction The IRF5 gene belongs to a family of transcription factors involved in modulating cell growth, differentiation, apoptosis, and immune system activity. A growing body of evidence indicates that immunological alterations are invo…

article 2016
Minerva ginecologica

BACKGROUND: Endometriosis is a disease with an unknown pathogenesis that can lead to infertility. Endometrial polyps, fibroids, and polycystic ovarian syndrome (PCOS) have relatively high frequency and are causes of infertility. We hypothes…

article 2016

Aberrant FOXP3 gene expression in eutopic and ectopic endometrium of infertile women with endometriosis orIgInal

article 2016
Journal of assisted reproduction and genetics ·doi:10.1007/s10815-016-0822-1
article 2016

Aspiration and ethanol sclerotherapy to treat recurrent ovarian endometriomas prior to in vitro fertilization – a pilot study Aspiração e alcoolização de endometriomas ovarianos recorrentes prévios ao tratamento de fertilização in vitro – e…

article 2015
·doi:10.3823/1605

Background: Immunological theories suggest that changes in the immune system could prevent the ability to eliminate the endometrium of the pelvic cavity. In women with endometriosis is possible that changes in immunity mediated by T cells f…

review 2015
Archives of gynecology and obstetrics ·doi:10.1007/s00404-015-3705-2
other 2015
Journal of assisted reproduction and genetics ·doi:10.1007/s10815-015-0523-1

PURPOSE: Recently, several genome-wide association studies have demonstrated an association between endometriosis and markers located in or near to WNT4 gene. In order to assess the validity of the findings, we conducted a replication case-…

article 2015
·doi:10.1016/j.fertnstert.2015.07.518
article 2015
Archives of gynecology and obstetrics ·doi:10.1007/s00404-015-3808-9