Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Recent research on gene polymorphisms related to caffeine therapy in preterm infants with apnea of prematurity].

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics - 15 Jul 2022

Xie Jiang-Biao, Lin Xin-Zhu

Abstract excerpt

Apnea of prematurity (AOP) is one of the common diseases in preterm infants. The main cause of AOP is immature development of the respiratory control center. If AOP is not treated timely and effectively, it will lead to respiratory failure, hypoxic brain injury, and even death in severe cases. Caffeine is the first choice for the treatment of AOP, but its effectiveness varies in preterm infants. With the...

Topics

Join the communities discussing this publication.

Apnea
Caffeine
Infant
Infant, Newborn
Infant, Newborn, Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Infant, Premature

Infant, Premature, Diseases

Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 35894202
DOI: 10.7499/j.issn.1008-8830.2203134
PMCID: PMC9336620

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Recent research on gene polymorphisms related to caffeine therapy in preterm infants with apnea of prematurity].PMID 35894202Read ↗

Genetic basis of apnoea of prematurity and caffeine treatment response: role of adenosine receptor polymorphisms: genetic basis of apnoea of prematurity.Semantic proximity Read ↗

Caffeine Therapy for Apnea of Prematurity: Role of the Circadian CLOCK Gene PolymorphismSemantic proximity Read ↗

The association of gene polymorphisms of adenosine and dopamine receptors with the response to caffeine citrate treatment in infants with apnea of prematurity: a prospective nested case-control study.Semantic proximity Read ↗

Monitoring blood caffeine concentration in preterm infants: a retrospective observational studySemantic proximity Read ↗

[Research progress of the gene polymorphisms of metabolic enzyme related to polycyclic aromatic hydrocarbons risk of preterm birth].Semantic proximity Read ↗

[Assessing the impact of risk factors and polymorphisms GST genes on the development of bronchopulmonary dysplasia in premature infants].Semantic proximity Read ↗

Heritability of apnea of prematurity: a retrospective twin study.Semantic proximity Read ↗

The Role of Genetic Polymorphisms in Antioxidant Enzymes and Potential Antioxidant Therapies in Neonatal Lung DiseaseSemantic proximity Read ↗

[Genotype and phenotype analysis of neonates with neonatal encephalopathy complicated with perinatal hypoxic event].Semantic proximity Read ↗

[Mutations of MTHFR, MTR, MTRR genes as high risk factors for neural tube defects].Semantic proximity Read ↗

Correlation of interactions between NOS3 polymorphisms and oxygen therapy with retinopathy of prematurity susceptibility.Semantic proximity Read ↗

Antioxidant and neurodevelopmental gene polymorphisms in prematurely born individuals influence hypoxia-related oxidative stress.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.