Illescas Tamara, Mansilla Elena, Herrero Beatriz, Rodríguez Roberto, López Francisco, Aza-Carmona Miriam, Regojo Rita María, Santos-Simarro Fernando, Heath Karen E, Bartha José Luis, Antolín Eugenia
Fetal Medicine Unit, Department of Obstetrics and Gynecology, Hospital Universitario La Paz, Madrid, Spain.
Institute of Medical and Molecular Genetics (INGEMM), Hospital Universitario La Paz, Madrid, Spain.
Eur J Obstet Gynecol Reprod Biol. 2020 Jul;250:209-215. doi: 10.1016/j.ejogrb.2020.05.009. Epub 2020 May 19.
To assess the diagnostic accuracy of prenatal ultrasound for detecting fetal skeletal dysplasias and to describe its role in orienting genetic studies.
Observational study of pregnant women surveyed in our hospital, between 2011 and 2018, with fetal long bones below the 3rd centile (shortened long bones), either as an isolated finding or associated to other skeletal anomalies. We used a systematic protocol for the ultrasound evaluation and selection of those fetuses suspected of having a skeletal dysplasia. We report the demographics of these patients along with the sonographic follow-up of their fetuses, the genetic results and the outcome of the pregnancies and the newborn in the entire group and also compare data between the two sub-groups (isolated shortened long bones vs shortened long bones associated to other anomalies).
A total of 81 pregnancies with a suspected fetal skeletal dysplasia were included, with a complete follow-up available in 75 cases, 22 with isolated shortened long bones and 53 cases that presented shortened long bones with other skeletal anomalies. In the shortened long bones sub-group, a total of five (23 %) were born healthy neonates, 10 (45 %) were small for gestational age or intrauterine growth restricted (one of them of genetic origin) and seven (32 %) had a skeletal dysplasia (6 of them with genetic diagnosis). Whilst among the 53 cases that presented with shortened long bones + other skeletal anomalies, three (6%) were healthy neonates, five (9%) were small for gestational age/intrauterine growth restricted (two of genetic origin) and 45 (85 %) had a skeletal dysplasia (19 genetically confirmed and 26 with a clinical diagnosis). These differences in frequencies between the two sub-groups were determined to be statistically significant (χ: p = 0.02).
Around one third of fetuses with isolated shortened long bones will have a skeletal dysplasia. If abnormal skeletal ultrasound findings are associated with shortened long bones, the risk for skeletal dysplasia is significantly increased (85 %). Prenatal systematic approach in a multidisciplinary unit is useful in the orientation of genetic studies.
评估产前超声检测胎儿骨骼发育不良的诊断准确性,并描述其在指导基因研究中的作用。
对2011年至2018年在我院接受检查的孕妇进行观察性研究,这些孕妇的胎儿长骨低于第3百分位数(长骨缩短),可为孤立性发现或与其他骨骼异常相关。我们采用系统方案对怀疑有骨骼发育不良的胎儿进行超声评估和筛选。我们报告这些患者的人口统计学数据,以及对其胎儿的超声随访、基因检测结果、妊娠结局和新生儿情况,并比较两个亚组(孤立性长骨缩短与伴有其他异常的长骨缩短)之间的数据。
共纳入81例疑似胎儿骨骼发育不良的妊娠病例,75例有完整随访资料,其中22例为孤立性长骨缩短,53例长骨缩短并伴有其他骨骼异常。在长骨缩短亚组中,共有5例(23%)出生时为健康新生儿,10例(45%)为小于胎龄儿或宫内生长受限(其中1例为基因源性),7例(32%)有骨骼发育不良(其中6例有基因诊断)。而在53例长骨缩短并伴有其他骨骼异常的病例中,3例(6%)为健康新生儿,5例(9%)为小于胎龄儿/宫内生长受限(其中2例为基因源性),45例(85%)有骨骼发育不良(19例基因确诊,26例临床诊断)。两个亚组之间这些频率差异具有统计学意义(χ:p = 0.02)。
约三分之一孤立性长骨缩短的胎儿会有骨骼发育不良。如果骨骼超声异常表现与长骨缩短相关,骨骼发育不良的风险会显著增加(85%)。多学科单位的产前系统方法有助于指导基因研究。