Hook E B, Cross P K
Bureau of Child Health, New York State Department of Health, Albany 12237.
Ann Hum Genet. 1987 Jan;51(1):27-55. doi: 10.1111/j.1469-1809.1987.tb00864.x.
We report data on diagnoses made on amniotic fluid specimens from 1977 to 1984 as reported to the New York State Chromosome Registry. The rate of all de novo (presumed mutant) abnormalities was about 2 per 1,000 in about 61,000 fetuses in which results are unlikely to be biased by the reason for amniocentesis (except for maternal age). This includes about 0.5 per 1,000 de novo markers, about 0.5 per 1,000 other de novo unbalanced, and about 1.0 per 1,000 de novo balanced rearrangements. In about 55,000 fetuses in which rates of inherited abnormalities could be evaluated without apparent bias, the rate of all inherited rearrangement was about 2.9 per 1,000. This includes about 0.3 per 1,000 inherited markers, about 0.2 per 1,000 other inherited unbalanced rearrangements, and about 2.4 per 1,000 inherited balanced abnormalities. Only mutant markers showed a clear association with maternal age (37.6 +/- 2.7 in 24 cases v. 35.8 +/- 3.6 in controls). Inherited markers did not exhibit this trend (35.8 +/- 2.0 in 12 cases v. 36.4 +/- 2.8 in controls). Paternal age does not appear to account for the association. Among abnormalities of known origin, the ratio of mutant to inherited cases is for markers 64:36, for other unbalanced rearrangements 73:27, and for all balanced abnormalities 29:71. In a subgroup of about 55,000 fetuses, of 263 total abnormalities there were 8 instances of apparent true somatic mosaics (5 mutant and 3 of unknown origin but almost certainly mutant). There were also 20 instances of markers in which presumptive somatic loss had resulted in mosaicism (10 mutant, 6 of unknown origin and 4 inherited) and 13 other instances of mosaicism associated with apparent somatic loss (9 mutant, 3 of unknown origin, and 1 inherited). The sex ratio (Y to non-Y karyotypes) for all abnormalities detected was 228:210 (1.09), not different from controls. Only deletions (5:14) and 'other' unbalanced rearrangements (5:13) exhibited a suggestive deviation from this trend. The rates of mutant chromosome rearrangements reported from 1977 to 1983 showed no apparent time cluster, with the possible exception of a peak of markers in 1977, a trend that may be due to higher maternal age in this year. Among fetuses studied because of maternal exposure to putative mutagens there was a non-significant excess of mutants (2.9-5.7 per 1,000 v. 1.7-2.2 per 1,000) and a borderline significant excess of inherited rearrangements (8.6-11.5 per 1,000 v. 2.6-3.1 per 1,000).(ABSTRACT TRUNCATED AT 400 WORDS)
我们报告了1977年至1984年期间向纽约州染色体登记处报告的羊水样本诊断数据。在约61,000例胎儿中,所有新发(推测为突变型)异常的发生率约为每1000例中有2例,这些胎儿的结果不太可能因羊水穿刺的原因(除母亲年龄外)而产生偏差。这包括每1000例中约0.5例新发标记物、每1000例中约0.5例其他新发不平衡异常以及每1000例中约1.0例新发平衡重排。在约55,000例可在无明显偏差情况下评估遗传异常发生率的胎儿中,所有遗传重排的发生率约为每1000例中有2.9例。这包括每1000例中约0.3例遗传标记物、每1000例中约0.2例其他遗传不平衡重排以及每1000例中约2.4例遗传平衡异常。只有突变标记物显示出与母亲年龄有明显关联(24例中为37.6±2.7,对照组为35.8±3.6)。遗传标记物未呈现此趋势(12例中为35.8±2.0,对照组为36.4±2.8)。父亲年龄似乎无法解释这种关联。在已知起源的异常中,突变型与遗传型病例的比例在标记物方面为64:36,在其他不平衡重排方面为73:27,在所有平衡异常方面为29:71。在约55,000例胎儿的亚组中,在总共263例异常中有8例明显的真正体细胞镶嵌体(5例突变型,3例来源不明但几乎肯定是突变型)。还有20例标记物,其中推测的体细胞丢失导致了镶嵌体(10例突变型,6例来源不明,4例遗传型)以及13例与明显体细胞丢失相关的其他镶嵌体实例(9例突变型,3例来源不明,1例遗传型)。检测到的所有异常的性别比(Y与非Y核型)为228:210(1.09),与对照组无差异。只有缺失(5:14)和“其他”不平衡重排(5:13)显示出与该趋势有提示性偏差。1977年至1983年报告的突变染色体重排发生率未显示出明显的时间聚集,1977年标记物可能出现一个峰值除外,这一趋势可能归因于该年较高的母亲年龄。在因母亲接触假定诱变剂而研究的胎儿中,突变型有非显著的过量(每1000例中有2.9 - 5.7例对1.7 - 2.2例),遗传重排有临界显著的过量(每1000例中有8.6 - 11.5例对2.6 - 3.1例)。(摘要截短于400字)