Evidence map›Paper›PMID 41974762›Full record

ArticleScientific reports2026

Prenatal diagnosis strategies and pregnancy outcomes in the Luohe region of China in the context of increasing maternal age.

Shaozhe Yang, Rongxiang Li, Zhenhua Gong, Shuwen Xin, Yanqi He, Shaoxia Teng, Yanan Gao, Xiuhong Fu

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Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Shaozhe YangHenan Key Laboratory of Fertility Protection and Aristogenesis, Luohe Central Hospital, 54 Renmin East Road, Shaoling District, Luohe, 462000, Henan, People's Republic of China.
Rongxiang LiHenan Key Laboratory of Fertility Protection and Aristogenesis, Luohe Central Hospital, 54 Renmin East Road, Shaoling District, Luohe, 462000, Henan, People's Republic of China.
Zhenhua GongDepartment of Clinical Genetics, Huantai Maternal and Child Health Centre, Zibo, 256400, People's Republic of China.
Shuwen XinHenan Key Laboratory of Fertility Protection and Aristogenesis, Luohe Central Hospital, 54 Renmin East Road, Shaoling District, Luohe, 462000, Henan, People's Republic of China.
Yanqi HeHenan Key Laboratory of Fertility Protection and Aristogenesis, Luohe Central Hospital, 54 Renmin East Road, Shaoling District, Luohe, 462000, Henan, People's Republic of China.
Shaoxia TengHenan Key Laboratory of Fertility Protection and Aristogenesis, Luohe Central Hospital, 54 Renmin East Road, Shaoling District, Luohe, 462000, Henan, People's Republic of China.
Yanan GaoHenan Key Laboratory of Fertility Protection and Aristogenesis, Luohe Central Hospital, 54 Renmin East Road, Shaoling District, Luohe, 462000, Henan, People's Republic of China.
Xiuhong FuHenan Key Laboratory of Fertility Protection and Aristogenesis, Luohe Central Hospital, 54 Renmin East Road, Shaoling District, Luohe, 462000, Henan, People's Republic of China. lhscqzdzx@163.com.

Funding

Henan Key Laboratory of Fertility Protection and Aristogenesis SYLBHYSSYS
6 · The paper itself

Abstract

This article aims to explore prenatal diagnostic strategies in the context of increasing maternal age. We calculated the proportion of advanced maternal age (AMA) pregnancies in the Luohe region from 2019 to 2023 and evaluated the indications, abnormal fetal karyotypes, and pregnancy outcomes among 3681 pregnant women (3700 samples) who underwent amniocentesis. The prenatal diagnostic indications, abnormal fetal karyotypes, and pregnancy outcomes of 3681 pregnant women (3700 samples) were determined. The rates of abnormal amniotic fluid karyotypes for different indications and termination of pregnancy (TOP) rates with different types of abnormalities were compared. From 2019 to 2023, the proportion of AMA pregnancies in Luohe region increased from 11.30 to 16.03%. The most common prenatal diagnosis was AMA (54.50%), followed by abnormal maternal serum screening (35.83%). Among the 3700 samples, 97 exhibited numerical abnormalities, 32 structural abnormalities, and 2 had both numerical and structural abnormalities. The highest TOP rates were observed for combined numerical and structural abnormalities, followed by isolated numerical abnormalities and isolated structural abnormalities. Among numerical abnormalities, sex chromosome aneuploidies had a lower TOP rate than common trisomies and rare autosomal aneuploidies. AMA have become the primary prenatal diagnostic indication. In addition to noninvasive prenatal testing (NIPT), fetal karyotyping can also detect mosaicism, structural abnormalities, and triploidy. The combination of karyotyping and molecular detection has increased the detection rate of chromosomal abnormalities. However, NIPT cannot replace amniocentesis.

Indexed as

Advanced Maternal AgePregnancy OutcomePrenatal DiagnosisAbnormal KaryotypeAdultAmniocentesisAneuploidyChinaChromosome AberrationsChromosome DisordersFemaleHumansKaryotypingPregnancyAdvanced maternal ageAmniocentesisChromosome abnormalityKaryotype analysisPrenatal diagnosis

Identifiers

PMID41974762
PMCPMC13237138

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