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47,XYY 综合征的发病率:一项全国范围内医院诊断和药物使用的流行病学研究。

Morbidity in 47,XYY syndrome: a nationwide epidemiological study of hospital diagnoses and medication use.

机构信息

Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.

Department of Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark.

出版信息

Genet Med. 2020 Sep;22(9):1542-1551. doi: 10.1038/s41436-020-0837-y. Epub 2020 Jun 1.

DOI:10.1038/s41436-020-0837-y
PMID:32475987
Abstract

PURPOSE

A systematic description of morbidity in 47,XYY syndrome based on nationwide registry data of hospital diagnoses and prescribed medication.

METHODS

All males in Denmark diagnosed with 47,XYY syndrome during 1960-2014 were identified. Each was matched with 100 male controls from the general population. Diagnoses related to hospital encounters (1977-2014) and prescriptions (1996-2014) were analyzed by negative binominal regression and Cox regression, respectively.

RESULTS

47,XYY syndrome was associated with a significantly increased overall incidence of hospital diagnoses (incidence rate ratio = 2.30, confidence interval [CI]: 1.99-2.65), including a significantly increased incidence of diagnoses associated with congenital malformations and genetic disorders as well as with psychiatric, neurologic, respiratory, urogenital, endocrine, circulatory, gastrointestinal, and musculoskeletal system disorders. Diagnoses associated with infections, skin and eye disorders were significantly increased as well. 47,XYY syndrome was associated with a significantly increased occurrence of prescriptions overall (hazard ratio = 1.25, CI: 1.10-1.44), with sex hormones and medication related to the urogenital system, blood, and nervous system being most prominently increased.

CONCLUSION

47,XYY syndrome is associated with a significantly increased morbidity owing to a wide variety of diseases. Increased awareness of the diverse morbidity in 47,XYY syndrome may help guide clinicians assessing 47,XYY males, thereby improving long-term health outcomes.

摘要

目的

基于全国医院诊断和处方用药登记数据,对 47,XYY 综合征患者的发病率进行系统描述。

方法

确定丹麦所有在 1960-2014 年期间被诊断为 47,XYY 综合征的男性患者。每位患者均匹配 100 名来自普通人群的男性对照者。采用负二项回归和 Cox 回归分别分析与医院就诊(1977-2014 年)和处方(1996-2014 年)相关的诊断。

结果

47,XYY 综合征患者的总体医院诊断发病率显著升高(发病率比=2.30,95%置信区间[CI]:1.99-2.65),包括先天性畸形和遗传疾病以及精神、神经、呼吸、泌尿生殖、内分泌、循环、胃肠道和肌肉骨骼系统疾病的诊断发病率显著升高。与感染、皮肤和眼部疾病相关的诊断发病率也显著升高。47,XYY 综合征患者的总体处方发生情况显著升高(风险比=1.25,95%CI:1.10-1.44),与泌尿生殖系统、血液和神经系统相关的性激素和药物显著增加。

结论

47,XYY 综合征患者的发病率显著升高,与多种疾病有关。提高对 47,XYY 综合征患者多种发病率的认识,可能有助于指导评估 47,XYY 男性患者的临床医生,从而改善其长期健康结局。

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本文引用的文献

1
The XYY syndrome: a follow-up study on 38 boys.XYY综合征:对38名男孩的随访研究。
Genet Couns. 2003;14(3):267-79.
2
Maldescendus testis.睾丸下降不全
Horm Res. 1999 Dec;51(6):261-9. doi: 10.1159/000023412.
3
Summary of clinical findings: profiles of children with 47,XXY, 47,XXX and 47,XYY karyotypes.临床发现总结:47,XXY、47,XXX和47,XYY核型儿童的概况。
X和Y基因剂量效应是人类性别二态性的主要影响因素:以身高为例。
Proc Natl Acad Sci U S A. 2025 Jun 3;122(22):e2503039122. doi: 10.1073/pnas.2503039122. Epub 2025 May 19.
4
Prevalence and disease risks for male and female sex chromosome trisomies: a registry-based phenome-wide association study in 1.5 million participants of MVP, FinnGen, and UK Biobank.男性和女性性染色体三体的患病率及疾病风险:一项基于MVP、芬兰基因库和英国生物银行150万参与者的全表型组关联登记研究。
medRxiv. 2025 Feb 2:2025.01.31.25321488. doi: 10.1101/2025.01.31.25321488.
5
Peripheral immune cell abundance differences link blood mitochondrial DNA copy number and Parkinson's disease.外周免疫细胞丰度差异与血液线粒体DNA拷贝数及帕金森病相关联。
NPJ Parkinsons Dis. 2024 Nov 14;10(1):219. doi: 10.1038/s41531-024-00831-x.
6
Giftedness and atypical sexual differentiation: enhanced perceptual functioning through estrogen deficiency instead of androgen excess.天赋与非典型性性分化:雌激素缺乏而非雄激素过多增强感知功能。
Front Endocrinol (Lausanne). 2024 May 1;15:1343759. doi: 10.3389/fendo.2024.1343759. eCollection 2024.
7
Prevalence, Morbidity, and Mortality of Men With Sex Chromosome Aneuploidy in the Million Veteran Program Cohort.百万退伍军人计划队列中性染色体非整倍体男性的患病率、发病率和死亡率。
JAMA Netw Open. 2024 Mar 4;7(3):e244113. doi: 10.1001/jamanetworkopen.2024.4113.
8
Confusing finding of quantitative fluorescent polymerase chain reaction analysis in invasive prenatal genetic diagnosis: A case report.侵入性产前基因诊断中荧光定量聚合酶链反应分析的困惑发现:一例报告
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9
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Endocr Connect. 2023 Aug 1;12(9):e220440. doi: 10.1530/EC-22-0440.
10
The multi-omic landscape of sex chromosome abnormalities: current status and future directions.性染色体异常的多组学格局:现状与未来方向
Endocr Connect. 2023 Aug 1;12(9):e230011. doi: 10.1530/EC-23-0011.
Birth Defects Orig Artic Ser. 1979;15(1):261-6.