Spontaneous preterm birth: advances toward the discovery of genetic predisposition

JF Strauss III, R Romero, N Gomez-Lopez… - American journal of …, 2018 - Elsevier
Evidence from family and twin-based studies provide strong support for a significant
contribution of maternal and fetal genetics to the timing of parturition and spontaneous …

Spontaneous preterm birth and single nucleotide gene polymorphisms: a recent update

IA Sheikh, E Ahmad, MS Jamal, M Rehan, M Assidi… - BMC genomics, 2016 - Springer
Background Preterm birth (PTB), birth at< 37 weeks of gestation, is a significant global public
health problem. World-wide, about 15 million babies are born preterm each year resulting in …

Meta-analysis of maternal and fetal transcriptomic data elucidates the role of adaptive and innate immunity in preterm birth

B Vora, A Wang, I Kosti, H Huang, I Paranjpe… - Frontiers in …, 2018 - frontiersin.org
Preterm birth (PTB) is the leading cause of newborn deaths around the world. Spontaneous
preterm birth (sPTB) accounts for two-thirds of all PTBs; however, there remains an unmet …

Matrix metalloproteinase and tissue inhibitors of metalloproteinases gene polymorphisms in disorders that influence fertility and pregnancy complications: A …

A Barišić, SD Pavlić, S Ostojić, N Pereza - Gene, 2018 - Elsevier
Matrix metalloproteinase (MMP) and tissue inhibitors of metalloproteinase (TIMP) gene
polymorphisms have been extensively evaluated as predisposing factors to human …

Current approaches to risk assessment and prevention of preterm birth—a continuing public health crisis

JR Biggio - Ochsner Journal, 2020 - ochsnerjournal.org
Background: Preterm birth remains a major cause of neonatal morbidity and mortality.
Several potential pathways and pathophysiologic processes can lead to preterm birth …

The genomics of prematurity in an era of more precise clinical phenotyping: A review

TA Manuck - Seminars in Fetal and Neonatal Medicine, 2016 - Elsevier
Spontaneous preterm birth is a major public health problem, with a clear genetic component.
Genetic association studies have evolved substantially in recent years, moving away from …

Functional polymorphisms of matrix metalloproteinases 1 and 9 genes in women with spontaneous preterm birth

N Pereza, I Pleša, A Peterlin, Ž Jan, N Tul… - Disease …, 2014 - Wiley Online Library
Objective. The aim of this study was to investigate the association of functional MMP-1‐1607
1G/2G and MMP-9‐1562 C/T gene polymorphisms with spontaneous preterm birth (SPTB; …

TNFRSF1B Gene Variants in Clinicopathological Aspects and Prognosis of Patients with Cutaneous Melanoma

BF Carvalho, GVB Gomez, J Carron… - International Journal of …, 2024 - mdpi.com
Regulatory T lymphocytes play a critical role in immune regulation and are involved in the
aberrant cell elimination by facilitating tumor necrosis factor connection to the TNFR2 …

The burden of genetic and epigenetic traits in prematurity

B Ribeiro de Andrade Ramos… - Reproductive …, 2018 - journals.sagepub.com
Despite decades of investigations and accumulated scientific knowledge, preterm birth
(PTB) remains a significant burden worldwide. Several mechanisms have been proposed to …

Maternal genetic risk factors for spontaneous preterm birth: A systematic review and meta‐analysis

T Mladenić, A Barišić, N Pereza… - … of Gynecology & …, 2024 - Wiley Online Library
Background Despite various genomic approaches used in prior studies investigating the
association of maternal genetic variability with spontaneous preterm birth (sPTB), results …