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The Children of Atomic Bomb Survivors: A Genetic Study (1991)

Chapter: Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki

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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

8

Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki

A.A.AWA1, T.HONDA2, S.NERIISHI3, T.SUFUNI1,4, H.SHIMBA1, K.OHTAKI1, M.NAKANO1, Y.KODAMA1, M.ITOH2, and H.B.HAMILTON5

1 Introduction

A cytogenetic study of the children born to atomic bomb survivors in Hiroshima and Nagasaki and children born to unexposed parents was initiated in 1967 (Awa 1975; Awa et al. 1968). The study was expanded in 1976 as a part of the Genetic Platform Research Program at RERF (Radiation Effects Research Foundation), and has been continued to the present time in conjunction with the ongoing mortality study and biochemical genetics survey on the F1 progeny (RERF Research Protocol 1975).

The main objective of the present study is to evaluate the radiation sensitivity of human germ-cell chromosomes by measuring the frequency of children with chromosome changes in structure or number induced by radiation in the germ cells of exposed parents. It is expected that stable chromosome aberrations, if induced in the germ cells, would be most likely transmitted to the offspring. Although there is no evidence of chromosome aneuploidy being induced by radiation exposure in humans, it is difficult to exclude the possibility that abnormalities, such as XYY and XXX, would be induced in the offspring.

The present chapter describes the results of somatic chromosome analysis of 8,322 children born to A-bomb survivors in Hiroshima and Nagasaki and 7,976 children born to parents who had received less than 1 rad (distally exposed) or were not in the cities (NIC) at the time of the bomb (ATB). Chromosome analyses were based mostly on nonbanded preparations throughout the study.

Because of the recent, extensive reassessment of A-bomb dosimetry by a US Japan team of experts (1st and 2nd US-Japan Joint Workshop 1983, 1984), the present study samples have been divided into exposed and control groups based on the T65DR system that has been routinely used until recently at RERF (Milton and Shohoji 1968). The data base for the new DS86 dose system has been entered into the RERF

1

Radiation Effects Research Foundation, 5–2 Hijiyama Park, Minami-ward Hiroshima 732, Japan

2

Department of Radiobiology, Nagasaki, Japan

3

Department of Clinical Studies, Nagasaki, Japan

4

Biological Safety Research Center, National Institute of Hygienic Sciences, Tokyo, Japan

5

RERF Consultant

Reproduced, with permission, from Cytogenetics, ed. by G.Obe and A.Basler, © Springer-Verlag, Berlin-Heidelberg, 1987.

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

computer; however, calculations of the individual dose estimates for each survivor are now in progress, but are not available at this time. For this reason, no attempt has been made to analyze the present data in terms of parental radiation doses.

2 Materials and Methods

The sample subjects of the present survey were selected primarily from the RERF F1 mortality study cohort (Kato et al. 1966). This cohort includes children born between 1 May 1946 and 31 December 1958 to parents, one or both of whom were the residents of Hiroshima and Nagasaki ATB. The samples were later expanded to include children who were born after 1959 through the end of 1972. The contribution of the extended samples was about 10% of the total.

In this analysis, the exposed group consists of children born to parents, one or both of whom were located within 2000 m from the hypocenter and who had T65DR dose estimates of more than 1 rad. The control group consisted of children born to parents (1) one or both of whom were exposed distally (2500 m or more from the hypocenter) with estimated doses of less than 1 rad, or (2) were not present in the city ATB.

About 40% of the total individuals in the original samples were not included in this study, because they had died (5%), or migrated outside the contactable areas of both cities (35%). Of the remaining individuals, approximately 74% agreed to participate in this study. Thus, the participation rate of this survey was 45% of the total original sample.

After obtaining consent from the F1 participants and, if necessary, their parents, they were invited to visit the RERF clinic. At that time they were interviewed by nurses to obtain medically-related information and a blood sample was drawn. If requested, a physical examination was performed.

Heparinized blood specimens, 1 to 2 ml per person, collected from each participant, were cultured for 2 days, and then harvested for chromosome preparations using the conventional Giemsa staining methods, the details of which have been described elsewhere (Awa et al. 1978).

In each case, ten well-spread metaphases were examined directly under the microscope, and three of them were photographed for detailed karyotype analysis. Cases with less than ten scorable metaphases were regarded as culture failure. The rate of failure was about 0.1% of the total blood samples in the two cities. When an abnormality was suspected, 100 or more cells were examined.

In addition to the conventional stain, both Q- and C-band preparations (Caspersson et al. 1971; Sumner 1972) were used as a routine procedure. The G-banding method of Seabright (1971) was also applied to cases suspected of having abnormality. When family studies were performed on probands with structural rearrangements, high resolution banding techniques (Yunis et al. 1978; Pai and Thomas 1980) were employed for the precise identification of breakpoints of the chromosomes involved in the aberrations. A description of the type of chromosome abnormalities was made following the standardized nomenclature of ISCN (1978, 1981, 1985).

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

Table 1. Number of F1 children examined

 

Number of cases

 
 

Males

Females

Total

Number of parental couples

Hiroshima

Control

 

2,477

2,635

5,112

4,242

 

Exposed:

Father

638

636

1,274

968

 

Mother

1,348

1,490

2,838

2,018

 

Both

274

330

604

467

 

Total

2,260

2,456

4,716

3,453

Nagasaki

Control

 

1,205

1,659

2,864

2,231

 

Exposed:

Father

543

623

1,166

802

 

Mother

912

1,123

2,035

1,305

 

Both

199

206

405

263

 

Total

1,654

1,952

3,606

2,370

Total

Control

 

3,682

4,294

7,976

6,473

 

Exposed:

Father

1,181

1,259

2,440

1,770

 

Mother

2,260

2,613

4,873

3,323

 

Both

473

536

1,009

730

 

Total

3,914

4,408

8,322

5,823

3 Results
3.1 Characteristics of the Study Sample

As shown in Table 1, the total number of children examined was 16,298 in the two cities; 9,828 in Hiroshima (4,716 exposed and 5,112 controls), and 6,470 in Nagasaki (3,606 exposed and 2,864 controls). The number of females predominated over males in both cities as well as in both the exposed and control groups. The exposed group was further divided into three categories by parental exposure status; i.e., children born to parents in which only the father was exposed, only the mother was exposed, or both parents were exposed.

Since efforts were made to collect as many cases as possible in the exposed group, the number of children per parental couple is considerably higher in the exposed group than in the controls (Table 1); 1.4 children per couple (or 8,322 in 5,823) in the exposed, and 1.2 per couple (or 7,976 in 6,473) in the controls, when the two cities were combined.

The mean age of the participants at examination was 24 in Hiroshima, and 23 in Nagasaki with a range between 12 and 38.

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

Table 2. Overall frequency of F1 children with chromosome abnormalities (per 1,000)

 

Rearrangements

 
 

Sex chromosomes

Balanced

Unbalanced

Trisomy

Total

No. of cases examined

Hiroshima

Control

 

17 (3.33)

16 (3.13)

0

0

33 (6.46)

5,112

 

Exposed:

Father

4 (3.14)

5 (3.92)

2 (1.57)

1 (0.78)

12 (9.42)

1,274

 

Mother

5 (1.76)

7 (2.47)

1 (0.35)

0

13 (4.58)

2,838

 

Both

3 (4.97)

2 (3.31)

0

0

5 (8.28)

604

 

Total

12 (2.54)

14 (2.97)

3 (0.64)

1 (0.21)

30 (6.36)

4,716

Nagasaki

Control

 

7 (2.44)

9 (3.14)

2 (0.70)

0

18 (6.28)

2,864

 

Exposed:

Father

3 (2.57)

3 (2.57)

1 (0.86)

0

7 (6.00)

1,166

 

Mother

4 (1.97)

0

1 (0.49)

0

5 (2.46)

2,035

 

Both

0

1 (2.47)

0

0

1 (2.47)

405

 

Total

7 (1.94)

4 (1.11)

2 (0.55)

0

13 (3.61)

3,606

Total

Control

 

24 (3.01)

25 (3.13)

2 (0.25)

0

51 (6.39)

7,976

 

Exposed:

Father

7 (2.87)

8 (3.28)

3 (1.23)

1 (0.41)

19 (7.79)

2,440

 

Mother

9 (1.85)

7 (1.44)

2 (0.41)

0

18 (3.69)

4,873

 

Both

3 (2.97)

3 (2.97)

0

0

6 (5.95)

1,009

 

Total

19 (2.28)

18 (2.16)

5 (0.60)

1 (0.12)

43 (5.17)

8,322

Newborn infantsa

 

127 (2.23)

110 (1.93)

34 (0.60)

82 (1.44)

353 (6.20)

56,952

a Cited from Hook and Hamerton (1977).

3.2 Types and Frequencies of Chromosome Abnormalities

The results of the cytogenetic observations are shown in Table 2, and every abnormal case is fully described in the Appendix Table (see pp. 181–183).

Chromosome abnormalities are classified into the following three groups; (1) sex chromosome abnormalities, (2) autosomal structural rearrangements, and (3) autosomal trisomics.

3.2.1 Sex Chromosome Abnormalities

As shown in Table 3, there were 43 cases with sex chromosome anomalies; 19 of 8,322 in the exposed group (2.28 per 1,000) and 24 of 7,976 in the controls (3.01 per 1,000). No increased frequency of sex chromosome abnormalities, ascribable to parental radiation exposure, was observed.

The majority of the abnormalities was due to sex chromosome aneuploidy, mostly XYY and XXY in males and XXX in females, which constituted 75% of the total sex

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

Table 3. Frequency of F1 children with sex chromosome abnormalities (per 1,000)a

 

Males

Females

 

XYY

XXY

Mosaic

Other

Total

X

XXX

Mosaic

Other

Total

Hiroshima

Control

 

5 (2.02)

4 (1.61)

0

2 (0.81)

11 (4.44)

0

3 (1.14)

3 (1.14)

0

6 (2.28)

 

Exposed:

Father

0

1 (1.57)

1 (1.57)

0

2 (3.13)

0

2 (3.14)

0

0

2 (3.14)

 

Mother

0

4 (2.97)

0

0

4 (2.97)

0

1 (0.67)

0

0

1 (0.67)

 

Both

0

1 (3.65)

0

0

1 (3.65)

0

1 (3.03)

1 (3.03)

0

2 (6.06)

 

Total

0

6 (2.65)

1 (0.44)

0

7 (3.10)

0

4 (1.63)

1 (0.41)

0

5 (2.04)

Nagasaki

Control

 

0

5 (4.15)

0

0

5 (4.15)

0

1 (0.60)

0

1 (0.60)

2 (1.21)

 

Exposed:

Father

2 (3.68)

0

0

0

2 (3.68)

0

1 (1.61)

0

0

1 (1.61)

 

Mother

1 (1.10)

1 (1.10)

0

1 (1.10)

3 (3.29)

0

0

1 (0.89)

0

1 (0.89)

 

Both

0

0

0

0

0

0

0

0

0

0

 

Total

3 (1.81)

1 (0.60)

0

1 (0.60)

5 (3.02)

0

1 (0.51)

1 (0.51)

0

2 (1.02)

Total

Control

 

5 (1.36)

9 (2.44)

0

2 (0.54)

16 (4.35)

0

4 (0.93)

3 (0.70)

1 (0.23)

8 (1.86)

 

Exposed:

Father

2 (1.69)

1 (0.85)

1 (0.85)

0

4 (3.39)

0

3 (2.38)

0

0

3 (2.38)

 

Mother

1 (0.44)

5 (2.21)

0

1 (0.44)

7 (3.10)

0

1 (0.38)

1 (0.38)

0

2 (0.77)

 

Both

0

1 (2.11)

0

0

1 (2.11)

0

1 (1.87)

1 (1.87)

0

2 (3.73)

 

Total

3 (0.77)

7 (1.79)

1 (0.26)

1 (0.26)

12 (3.07)

0

5 (1.13)

2 (0.45)

0

7 (1.59)

Newborn infantsb

 

35 (0.93)

35 (0.93)

14 (0.37)

14 (0.37)

98 (2.59)

2 (0.10)

20 (1.04)

7 (0.37)

0

29 (1.51)

No. of cases

 

37,779

 

19,173

a The rates for the sex chromosome abnormalities apply only to the affected sex.

b Cited from Hook and Hamerton (1977).

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

anomaly cases. Except for mosaic situations, no female with 45,X was detected in any of the groups studied.

When the data from the two cities were combined, there were no significant differences between the frequencies of sex chromosome abnormalities in the exposed group when compared to the controls.

The frequency of mosaic cases was higher in females (2 in 4,408 exposed and 3 in 4,294 controls) than in males (1 in 3,914 exposed). Among the mosaics, there was a woman showing a mosaic of 45,X/46,X,r(X) in the Hiroshima controls. A family study revealed that the abnormality was identified as a de novo mutant since both parents showed the normal karyotype.

There were three cases with structural rearrangements involving sex chromosomes, all of which belonged to the control group; two unrelated males, each with a pericentric inversion of the Y-chromosome in Hiroshima, and a female with a distally deleted long arm of one of the X-chromosomes in Nagasaki.

One unusual observation was made in the Nagasaki series. A male child, born to an exposed mother, was found to have 46 chromosomes with two X-chromosomes (46,XX).

3.2.2 Autosomal Structural Rearrangements

3.2.2.1 Balanced. The majority of structural rearrangements involving autosomes were translocations of the Robertsonian or reciprocal types and pericentric inversions. They would, therefore, result in no loss or gain of chromosome material, and would be genetically balanced without any phenotypic effect. In the present study sample, there were occasionally two or more sibs in a family showing the identical karyotypic abnormality.

Among these cases, there were ten children (seven D/D and three D/G) from eight families with Robertsonian translocations in the exposed group, and six children (all D/D) from three families with similar rearrangements in the controls. By the same token, there were seven children from five families in the exposed group, and 13 children from 12 families in the controls with reciprocal translocations. Only one child in the exposed, and six children from five families in the controls had inversions.

An examination of Table 4 shows that an unusually high incidence of pericentric inversions was observed in the Hiroshima controls, and in Nagasaki a strikingly high rate of reciprocal translocations was observed in the controls, while no such cases were found in the exposed group.

As shown in the Appendix Table, chromosomes 5 and 8 were found to be involved more frequently than the others in the formation of reciprocal translocations. Furthermore, there was a frequent involvement of a chromosome 2 in pericentric inversions in Hiroshima.

In Table 5, pooled data on the frequencies of balanced structural rearrangements are tabulated in terms of the number of families in which they are observed as a function of total families included in the study. Although there is no significant difference in the frequencies of families with stable autosomal rearrangements, a relatively low frequency of rearrangements was observed in the exposed group in Nagasaki. The data

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

Table 4. Frequency of F1 children with structural rearrangements (per 1,000)

 

Balanceda

Unbalanceda

 

rob(D/D)

rob (D/G)

rcp

inv

Total

rob

rcp

del

supern

other

Total

Hiroshima

Control

4 (0.78)

0

6 (1.17)

6 (1.17)

16 (3.13)

0

0

0

0

0

0

Exposed:

 

Father

2 (1.57)

0

3 (2.35)

0

5 (3.92)

0

0

0

1 (0.78)

1 (0.78)

2 (1.57)

Mother

3 (1.06)

1 (0.35)

2 (0.70)

1 (0.35)

7 (2.47)

0

0

0

0

1 (0.35)

1 (0.35)

Both

0

0

2 (3.31)

0

2 (3.31)

0

0

0

0

0

0

Total

5 (1.06)

1 (0.21)

7 (1.48)

1 (0.21)

14 (2.97)

0

0

0

1 (0.21)

2 (0.42)

3 (0.64)

Nagasaki

Control

2 (0.70)

0

7 (2.44)

0

9 (3.14)

0

0

0

0

2 (0.70)

2 (0.70)

Exposed:

 

Father

2 (1.72)

1 (0.86)

0

0

3 (2.57)

0

0

0

1 (0.86)

0

1 (0.86)

Mother

0

0

0

0

0

0

0

0

0

1 (0.49)

1 (0.49)

Both

0

1 (2.47)

0

0

1 (2.47)

0

0

0

0

0

0

Total

2 (0.55)

2 (0.55)

0

0

4 (1.11)

0

0

0

1 (0.28)

1 (0.28)

2 (0.55)

Total

Control

6 (0.75)

0

13 (1.63)

6 (0.75)

25 (3.13)

0

0

0

0

2 (0.25)

2 (0.25)

Exposed:

 

Father

4 (1.64)

1 (0.41)

3 (1.23)

0

8 (3.28)

0

0

0

2 (0.82)

1 (0.41)

3 (1.23)

Mother

3 (0.62)

1 (0.21)

2 (0.41)

1 (0.21)

7 (1.44)

0

0

0

0

2 (0.41)

2 (0.41)

Both

0

1 (0.99)

2 (1.98)

0

3 (2.97)

0

0

0

0

0

0

Total

7 (0.84)

3 (0.36)

7 (0.84)

1 (0.12)

18 (2.16)

0

0

0

2 (0.24)

3 (0.36)

5 (0.60)

Newborn infantsb

(56,952)

40 (0.70)

11 (0.19)

51 (0.90)

8 (0.14)

110 (1.93)

4 (0.07)

7 (0.12)

5 (0.09)

10 (0.18)

8 (0.14)

34 (0.60)

a Abbreviations: rob Robertsonian translocation; rcp reciprocal translocation; inv inversion; del deletion; supern supernumerary chromosome.

b Cited from Hook and Hamerton (1977).

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

Table 5. Frequency of autosomal structural rearrangements by parental couples

City

Groupa

No. of parental couples

No. of rearrangements

Rate (×10-3)

Hiroshima

E

3453

11

3.19

 

C

4242

13

3.06

 

T

7695

24

3.12

Nagasaki

E

2370

3

1.27

 

C

2231

7

3.14

 

T

4601

10

2.17

Combined

E

5823

14

2.40

 

C

6473

20

3.09

 

T

12296

34

2.77

Neonatesb

 

59542

113

1.90

a Abbreviations: E exposed; C control; T total.

b Cited from Jacobs (1981).

were further compared with the frequencies of the same types of abnormalities derived from cytogenetic surveys on 59,542 consecutive newborn infants (Jacobs 1981). The results obtained in this study of both exposed and control groups were approximately 50% higher than that reported for neonatal surveys.

Family studies of abnormal cases were undertaken to determine whether the observed structural rearrangements arose de novo or were inherited from one or the other parent (Table 6). Family studies in all cases were not possible because of death of parents, or because parents did not wish to cooperate in this study. When two or more sibs in a family were found to carry the identical rearrangement, however, their abnormalities were judged to be inherited, even though a family study may not have been done.

The ample evidence indicates that the majority of cases with rearrangements are heritable. There were only two de novo mutants identified. Both mutants (one in the exposed and one in the control group) were seen in the Hiroshima group. None have been detected so far in Nagasaki. The gametic mutation rates on structural rearrangements derived from the combined data were estimated as 1.72×10-4 in the exposed group, and 1.40×10-4 in the controls, respectively. These values did not deviate significantly from the value of 1.88×10-4 per gamete per generation in the liveborn infant survey (Jacobs 1981) (see Addendum p. 178).

3.2.2.2 Unbalanced. There were seven abnormal cases which were placed in this category; five in the exposed and two in the controls. All of them were characterized by the presence of an extra-small metacentric element (or elements), termed as “mar” according to the standardized nomenclature system (ISCN 1978, 1981, 1985). The element (or elements) was present either as a “supernumerary” piece of chromosomal

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

Table 6. Parental origin of balanced structural rearrangementsa

 

Hiroshimab

Nagasakib

H+Nb

Neonatesc

 

E

C

E

C

E

C

 

de novo

1

1

0

0

1

1

18

Inherited

5

5

1

5

6

10

73

Father

2

3

1

3

3

6

37

Mother

0

1

0

1

0

2

36

Undetermined

3

1

0

1

3

2

0

Total

6

6

1

5

7

11

91

Not studied

5

7

2

2

7

9

22

Mutation rate

(×10-4)

2.65

2.55

1.72

1.40

1.88

a Including reciprocal and Robertsonian translocations and pericentric inversions.

b Abbreviations: E exposed; C control.

c Cited from Jacobs (1981).

material, in addition to the normal chromosome complement in all cells, or was in the form of a mosaic (Table 4, Appendix Table). Five of the cases were mosaics (three exposed and two controls).

In one male observed in the Nagasaki controls, three extra minute elements, each of which differed in size and shape, existed as cell lines with different combinations of markers (Itoh et al. 1984). Family studies revealed that most of these abnormal cases of unbalanced type were found to arise as de novo mutants (see Appendix Table).

3.2.3 Autosomal Trisomics

There was only one male Downs syndrome case (47,XY,+21) born in 1966 to an exposed father in Hiroshima, whose age at cytogenetic examination was 15. No other trisomic cases, such as D- and E-trisomy, have been observed in the F1 population.

A summary of the overall frequencies of cases with abnormalities by parental exposure and by city is shown in Table 7. It can be seen that for sex chromosome abnormalities and structural rearrangements, the frequencies are consistently higher in the controls than in the exposed, and also higher in Hiroshima than in Nagasaki. Yet none of these differences are significantly different.

The data from the two cities were combined, regardless of parental radiation exposure, and each of the frequencies was compared with that of corresponding abnormalities in the cytogenetic surveys on 56,952 consecutive liveborn infants (Hook and

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

Hamerton 1977). Here again, the frequencies of both sex abnormalities and rearrangements were somewhat higher in the children included in this study as compared to the neonates. In contrast, the incidence of autosomal trisomics was strikingly decreased in our samples.

Table 7. Frequency of cases with chromosome abnormalities in the F1 population (per 1,000)

 

Exposed

Control

Hiroshima

Nagasaki

Combined

Neonatesa

No. of cases

8,322

7,976

9,828

6,470

16,298

56,952

Abnormalities:

 

Sex chromosomes

2.28

3.01

2.95

2.16

2.64

2.23

Autosomal rearrangement

 

Balanced

2.16

3.13

3.05

2.01

2.64

1.93

Unbalanced

0.60

0.25

0.31

0.62

0.43

0.60

Autosomal trisomy

0.12

0

0.10

0

0.06

1.44

Total

5.17

(43)

6.39

(51)

6.41

(63)

4.79

(31)

5.77

(94)

6.20

(353)

a Cited from Hook and Hamerton (1977).

3.2.3.1 Heteromorphic Variants. In the course of the present screening, there was a variety of heterochromatic variants as detected with the conventional staining method. Some of these cases were reanalyzed by the application of C-, Q-, and other banding techniques, and the results have been already reported elsewhere (Sofuni et al. 1978, 1980; Sofuni and Awa 1982). Of the heteromorphic variants observed, cases with inv(9p+q-), 1qh+, 9qh+, 16qh+, (C-band variants at the constitutive heterochromatic regions), Dp+, Gp+, Dps+, Gps+, DP-, Gp- (Q-band variants either deleted or enlarged satellites and/or short arms of acrocentric chromosomes) were identified with high frequency.

4 Discussion

As mentioned previously, the main objective of this study was to demonstrate whether there is any measurable increase in the frequency of children with chromosome abnormalities that might be associated with A-bomb radiation exposure of parental germ-cell chromosomes. This cytogenetic evaluation was conducted by comparing the frequencies of children born to A-bomb survivors with chromosome abnormalities, especially structural rearrangements, with children born to nonexposed parents.

The present results show that there are no statistically significant increases in the frequency of chromosome abnormalities among the children of the exposed. In fact, the frequency of both sex chromosome aneuploidy and structural rearrangements was higher in the controls than in the exposed.

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

This does not imply that genetic effects ascribable to parental A-bomb exposure have not occurred. It simply indicates that such effects have not been detectable by the current cytogenetic methods used. The reason for the absence of cytogenetic effects of A-bomb radiation on the children of the survivors remains unresolved. One of the possible interpretations is that germ cells with chromosome damage could have been eliminated either in the course of gametogenesis or in the very early period of gestation as “unrecognized” spontaneous abortions.

Extensive cytogenetic surveys on consecutive liveborn infants, undertaken as international collaborative studies in several European and North American countries, have provided very useful and relevant information on the natural incidence of various types of constitutional chromosome abnormalities in the human population (Sergovich et al. 1969; Lubs and Ruddle 1970; Friedrich and Nielsen 1973; Jacobs et al. 1974; Hamerton et al. 1975; Nielsen and Sillesen 1975; Walzer and Gerald 1977; also refer to Hook and Hamerton 1977 for review).

Cytogenetic data based on these surveys were compared with our present findings (Tables 2 to 4, and 7). It is apparent that the frequencies of both sex chromosome abnormalities and balanced rearrangements are slightly higher in our study than in the neonatal surveys. The situation is reversed when one compares unbalanced rearrangements and autosomal trisomics. It is known that most, but not all, situations where autosomal trisomy as well as unbalanced rearrangements are associated with physical malformations, are incompatible with life. Since the mean age of our study subjects was 24 years at examination, it is conceivable that most conceptions with these abnormalities do not survive for 2 or 3 decades even if they survived to term.

Recently, attempts have been made to reevaluate cytogenetic surveys of neonates using banding techniques in order to obtain more precise information on the frequency of abnormalities associated with structural chromosomal changes in the general human population (Lin et al. 1976; Buckton et al. 1980; Hansteen et al. 1982; Nielsen et al. 1982). The results obtained in such studies are discordant. Some studies indicated an increase in the frequency of reciprocal translocations (Hansteen et al. 1982), and inversions (Hansteen et al. 1982; Nielsen et al. 1982), or an increase in the Q-band variants (Lin et al. 1976). In contrast, the frequency of all types of chromosome abnormalities detected when G-banding techniques were used have been found to be similar to that observed previously when conventional stain preparations were used (Buckton et al. 1980). In our experience, there seemed to be no difference in the detectability of structural rearrangements between conventional stain and G- and Q-banding methods, although the latter were found to be more efficient in detecting heteromorphic variants than the conventional method.

Maeda et al. (1978) reported the results of a cytogenetic survey on 2,626 consecutive liveborn infants in Japan. They found nine cases with sex chromosome abnormalities (0.30%) and ten autosomal abnormalities, including five with Robertsonian translocation of the balanced type (0.19%), one with 13-trisomy associated with Robertsonian translocation (0.04%), one with a supernumerary marker (0.04%), and three with 21-trisomy (0.11%). Although the sample size of this survey was rather small, the results agreed to-a certain extent with our findings with respect to the frequency of sex chromosome abnormalities and types and patterns of autosomal abnormalities.

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

Table 8. Frequency of autosomal structural rearrangements

City

Groupa

No. of children

No. of rearrangements

Rate (×10-3)

Hiroshima

E

4716

14

2.97

 

C

5112

16

3.13

 

T

9828

30

3.05

Nagasaki

E

3606

4

1.11

 

C

2864

9

3.14

 

T

6470

13

2.01

Combined

E

8322

18

2.16

 

C

7976

25

3.13

 

T

16298

43

2.64

Neonatesb

 

59542

113

1.90

a Abbreviations: E exposed; C control; T total.

b Cited from Jacobs (1981).

The origin and cytogenetic features of an additional marker chromosome, often designated as a supernumerary chromosome, have been studied extensively (refer to Buckton et al. 1985). This marker chromosome is chracterized by a small metacentric element. Often it has a satellite (or satellites) at one or both distal ends. With regard to the presence of cases in the F1 carrying such a marker, it was interesting to observe that (1) the supernumerary was seen in all cells or existed in the form of a mosaic, and (2) the majority of the supernumeraries were do novo mutants without any phenotypic change. This finding led to the presumption that the origin of the markers in our cases might arise from a product of a Robertsonian translocation between the short arms of the D- and G-chromosomes.

There has been discrepancy concerning a possible association between maternal radiation and trisomy-21 (Uchida et al. 1961; Schull and Neel 1962; Uchida 1977). In the A-bomb exposed population, Schull and Neel (1962) reported that the frequency of children with Down syndrome born to exposed mothers (fathers not exposed) was 0.54 per 1,000 (3 in 5,579), and 1.27 per 1,000 (12 in 9,440) in children born to nonexposed mothers. These results suggest that no association exists between Down syndrome and maternal radiation. The present results do not indicate an increase in children with 21-trisomy or aneuploidy involving any other chromosome.

Finally, when the new A-bomb radiation dosimetry system (DS86) becomes available for estimating the dose for individual survivors, the present data will be reanalyzed to determine the relationship between the frequency of chromosome abnormalities observed in children as a function of parental gonadal dose.

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

Table 9. Parental origin of balanced structural rearrangementsa

 

Hiroshima

Nagasaki

H+N

Neonatesb

 

E

C

E

C

E

C

 

de novo

1

1

0

0

1

1

18

Inherited

8

8

2

7

10

15

73

Father

2

4

2

4

4

8

37

Mother

0

1

0

1

0

2

36

Undetermined

6

3

0

2

6

5

0

Total

9

9

2

7

11

16

91

(Not studied)

(5)

(7)

(2)

(2)

(7)

(9)

(22)

Gametic mutation rate (×10-4)

1.65

1.74

0.98

0.98

1.88

a Including reciprocal and Robertsonian translocations plus pericentric inversions.

b Cited from Jacobs (1981).

Abbreviations: E exposed; C control; H Hiroshima; N Nagasaki.

Addendum. In the test, we computed the gametic mutation rates of structural rearrangements of balanced type in our population in terms of the frequency of families with abnormality as a function of total families studied. However, it seems more appropriate to estimate the chromosomal mutation rate using the following formula:

For the gametic mutation rate, the value derived from the above formula is further divided by 2 (Jacobs 1981). The gametic mutation rates on structural rearrangements derived from the combined data in Tables 8 and 9 were estimated as 0.98×10-4 in the exposed, and 0.98×10-4 in the controls, respectively. These values were much lower than the value of 1.88×10-4 per gamete per generation in the liveborn infant survey (Jacobs 1981).

Acknowledgments. We are grateful to the Hiroshima and Nagasaki citizens for their willingness to voluntarily participate in this survey. Without their cooperation this study would not have been possible. Our thanks are due also to the following RERF staff members for their continued support throughout this survey: Drs. M.Otake and S.Fujita, Department of Statistics, Dr. Y.Shimizu, Department of Epidemiology, for sample selection and statistical advices; Drs. T.Amano, M.Soda, R.Hazama, and their associaes in the Nursing Section, Department of Clinical Studies, for their clinical assistance; public health nurses and clinical contactors in the Department of Research Support who obtained consent of the participants and arrangements for their visit to RERF. We are very much indebted to Messrs. S.Iida, K.Tanabe, Mrs. Y.Urakawa, and their colleagues in the Cytogenetics Laboratories in Hiroshima and Nagasaki for their continued technical support including blood cultures, chromosome preparations, microscope and karyotype analysis, and photographic works. We wish to thank Dr. C.W.Edington, Vice-Chairman of RERF, for his encouragement and for going through the manuscript.

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×

Appendix Table. Family studies of abnormal cases of the unbalanced type

 

Age at birth

 

Case No.

Sex

Age ATE

Year of birth

Mo

Fa

Exposure status

Type of abnormality

Remarks

 

Hiroshima

 

FH3321

M

28

1948

32

38

C

A1. 47,XYY

 

FH4305

M

22

1956

30

38

C

” ”

 

FH4998

M

29

1949

25

29

C

” ”

 

FH7308

M

17

1964

28

32

C

” ”

 

FH9913

M

15

1969

25

27

C

” ”

 

FH0757

M

17

1953

26

34

Mo

A2. 47,XXY

 

FH0801

M

22

1948

23

27

Fa

” ”

 

FH0815

M

13

1957

31

48

B

” ”

 

FH4223

M

22

1956

34

31

Mo

” ”

 

FH4727

M

29

1949

33

38

Mo

” ”

 

FH5953

M

26

1953

21

24

C

” ”

 

FH6415

M

30

1950

32

40

C

” ”

 

FH6662

M

28

1952

27

31

C

” ”

 

FH8632

M

24

1958

24

28

Mo

” ”

 

FH8718

M

33

1949

35

41

C

” ”

 

FH8454

M

17

1965

25

30

Fa

A3. 46,XY/47,XYY

46:48 cells, 47:152 cells

FH6505

M

24

1956

32

38

C

A4. 46,X,inv(Y)(p11.2q11.2)

 

FH7417

M

23

1958

33

31

C

” 46,X,inv(Y)(p11.2q11.23)pat

 

FH0492

F

21

1948

25

29

Fa

A6. 47,XXX

 

FH1870

F

15

1957

34

33

B

” ”

 

FH3886

F

30

1947

25

27

C

” ”

 

FH5852

F

21

1958

30

36

Mo

” ”

 

FH8291

F

24

1958

23

27

Fa

” ”

F2: one (liveborn)

FH8912

F

16

1967

37

39

C

” ”

Sib (dizygotic co-twin)—normal

FH9339

F

15

1967

28

30

C

” ”

 

FH0092

F

18

1949

33

36

B

A7. 45,X/47,XXX

45:95 cells, 47:4 cells

FH3033

F

22

1954

33

38

C

” ”

45:82 cells, 47:15 cells

FH8020

F

24

1957

24

28

C

” ”

45:44 cells, 47:49 cells. F2 :one (liveborn), also pregnant at examination

FH8590

F

33

1948

25

38

C

” 45,X/46,X,r(x)§

§de novo mutant. 45:141 cells, 46:59 cells

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×
 

Age at birth

 

Case No.

Sex

Age ATE

Year of birth

Mo

Fa

Exposure status

Type of abnormality

Remarks

FH0381

M

18

1951

21

30

Fa

B1. 45,XY,t(DqDq)

   

FH1988

F

16

1956

27

32

Mo

” 45,XX,t(DqDq)

Sibs

FH2443

F

21

1952

23

28

Mo

” 45,XX, ”

   

FH4989

M

28

1951

29

39

Mo

” 45,XY,t(13q14q)

   

FH6456

M

30

1949

24

27

C

” 45,XY,t(13q14q)

Sibs

FH6664

F

29

1951

26

29

C

” 45,XX, ”

   

FH6757

F

26

1954

29

32

C

” 45,XX, ”

   

FH6538

F

30

1950

20

23

C

” 45,XX,t(14q15q)

   

FH8096

F

16

1966

30

35

Fa

” 45,XX,t(13q14q)

   

FH3496

F

22

1954

26

34

Mo

B2. 45,XX,t(14q21q)

   

FH0405

F

18

1951

29

43

Fa

B3. 46,XX,t(5;11)(q13;p15)

Sibs

FH8076

M

33

1949

27

41

Fa

” 46,XY, ”

   

FH2209

F

26

1947

34

36

B

” 46,XX,t(5;17)(p13;q25)§

 

§de novo mutant

FH2210

F

26

1947

23

29

B

” 46,XX,t(5;8)(q22;p11.2)pat

   

FH2690

M

17

1957

23

27

Fa

” 46,XY,t(5;8)(q22;p11.2)pat

   

FH4493

M

29

1949

32

34

C

” 46,XY,t(6;12)(q15;q22)

   

FH4595

M

23

1955

27

30

C

” 46,XY,t(1;6)(q21;p21)

   

FH6611

F

29

1951

27

32

Mo

” 46,XX,t(3;8)(q21;q24.1)

Sibs

FH6771

M

26

1954

30

35

Mo

” 46,XY,

   

FH7342

F

32

1949

27

36

C

” 46,XX,t(12;13)(q21.32;p12.3)§

 

§de novo mutant

FH9219

M

25

1957

25

31

C

B3. 46,XY,t(5;7)(q15;p21)pat

   

FH9876

F

13

1970

29

30

C

” 46,XX,t(5;8)(q22;p11.2)pat

   

FH9922

M

13

1971

25

30

C

” 46,XY,t(6;8)(q13;q22)

   

FH1705

F

25

1946

34

35

C

B4. 46,XX,inv(2p+q—)

   

FH5672

M

32

1947

27

32

C

” 46,XY,inv(18)(p11.32q11.2)mat

   

FH6099

M

27

1953

27

38

Mo

” 46,XY,inv(2)(p11.2q13)

   

FH7331

F

16

1964

27

33

C

” 46,XX,inv(2)(p11.2q13)pat

Sibs

FH7333

F

14

1966

29

34

C

” 46,XX, ”

   

FH9118

M

35

1948

39

45

C

” 46,XY;inv(2)(p11.2q14.2)

   

FH9254

M

34

1949

27

34

C

” 46,XY,inv(5)(p15.3q13)

   

FH7361

F

24

1957

24

25

Fa

B8. 47,XX,+mar*§ (*minute)

 

§de novo mutant. F2 :one (liveborn)

FH6169

F

23

1956

28

28

Mo

B9. 46,XX/47,XX,+mar* (*minute)

 

46:9 cells, 47:91 cells

FH8980

M

14

1969

25

28

Fa

” 46,XY,del(18)(p11.1)/46,XY,i(18q)

 

del(18p): 181 cells, i(18q): 7 cells

FH7594

M

15

1966

25

25

Fa

C1. 47,XY,+21§

 

§de novo mutant

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×
 

Nagasaki

 

FN0217

M

13

1956

37

33

Mo

A1. 47,XYY

   

FN0486

M

21

1948

30

35

Fa

” ”

   

FN0970

M

19

1951

26

28

Fa

” ”

   

FN1717

M

26

1948

31

39

C

A2. 47,XXY

   

FN2696

M

18

1957

27

27

C

” ”    

FN4025

M

30

1948

27

31

Mo

” ”

   

FN4171

M

25

1953

22

19

C

” ”

   

FN4317

M

28

1951

40

45

C

” ”

   

FN6865

M

14

1970

25

29

C

” ”

   

FN3338

M

21

1956

25

30

Mo

A4. 46,XX

 

[XX male]

FN3252

F

22

1955

24

27

Fa

A6. 47,XXX

   

FN4237

F

31

1947

20

24

C

” ”

   

FN2120

F

18

1956

26

24

Mo

A7. 46,XX/47,XXX

 

46:3 cells, 47:96 cells

FN3202

F

21

1956

33

37

C

A8. 46,XXq-

   

FN4935

F

32

1948

32

46

C

B1. 45,XX,t(13q14q)pat

Sibs

FN4936

F

28

1952

36

50

C

” 45,XX,

   

FN5837

M

13

1969

32

34

Fa

” 45,XY,t(13q14q)pat

Sibs

FN5859

F

17

1965

29

31

Fa

45,XX,
   

FN0870

M

18

1952

23

31

B

B2. 45,XY,t(DqGq)

   

FN6530

F

14

1969

29

36

Fa

” 45,XX,t(14q21q)

   

FN1638

M

24

1950

21

22

C

B3. 46,XY,t(Cq-;17q+)pat

   

FN3068

F

28

1948

40

44

C

” 46,XX,t(18q+;20q-)

   

FN3948

M

21

1957

33

41

C

” 46,XY,t(1p–;12q+)mat

   

FN4419

F

32

1947

22

28

C

” 46,XX,t(2p–;8p+)

Sibs

FN4891

F

31

1949

24

30

C

” 46,XX,

   

FN4724

M

29

1951

24

29

C

” 46,XY,t(Bq–;Cq+)pat    

FN5049

F

29

1951

28

35

C

” 46,XX,t(2q–;13q+)

   

FN2357

F

26

1949

23

46

Fa

B8. 47,XX,+mar* mat (*minute)

   

FN3990

M

22

1957

40

37

C

B9. 46,XY/47,XY,+mar*§ (*minute)

 

§de novo mutant. 46:18 cells, 47:31 cells

FN4121

M

30

1948

20

29

Mo

” 46,XY/47,XY,+mar*§ (*minute)

 

§de novo mutant. 46:21 cells, 47:9 cells

FN6023

M

31

1951

23

24

C

” 46,XY/47,XY,+mar/48,XY,+mar×2§

 

§de novo mutant. Complex mosaic consisting of cell lines with 2 or 3 different minute markers of varying combinations.

[Abbreviations] ATE: At the time of examination. Age at birth: Parental age. Mo: Mother. Fa: Father. Exposure status: B-Both parents exposed. Fa=Father exposed. Mo-Mother exposed. C=Control.

Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×
Page 356
Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×
Page 357
Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×
Page 358
Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×
Page 359
Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×
Page 360
Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
×
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Suggested Citation:"Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki." National Research Council. 1991. The Children of Atomic Bomb Survivors: A Genetic Study. Washington, DC: The National Academies Press. doi: 10.17226/1800.
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The Children of Atomic Bomb Survivors: A Genetic Study Get This Book
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Do persons exposed to radiation suffer genetic effects that threaten their yet-to-be-born children? Researchers are concluding that the genetic risks of radiation are less than previously thought.

This finding is explored in this volume about the children of atomic bomb survivors in Hiroshima and Nagasaki—the population that can provide the greatest insight into this critical issue. Assembled here for the first time are papers representing more than 40 years of research. These documents reveal key results related to radiation's effects on pregnancy termination, sex ratio, congenital defects, and early mortality of children. Edited by two of the principal architects of the studies, J. V. Neel and W. J. Schull, the volume also offers an important comparison with studies of the genetic effects of radiation on mice.

The wealth of technical details will be immediately useful to geneticists and other specialists. Policymakers will be interested in the overall conclusions and discussion of future studies.

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