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Published in: BMC Medical Genetics 1/2006

Open Access 01-12-2006 | Research article

Influence of advanced age of maternal grandmothers on Down syndrome

Authors: Suttur S Malini, Nallur B Ramachandra

Published in: BMC Medical Genetics | Issue 1/2006

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Abstract

Background

Down syndrome (DS) is the most common chromosomal anomaly associated with mental retardation. This is due to the occurrence of free trisomy 21 (92–95%), mosaic trisomy 21 (2–4%) and translocation (3–4%). Advanced maternal age is a well documented risk factor for maternal meiotic nondisjunction. In India three children with DS are born every hour and more DS children are given birth to by young age mothers than by advanced age mothers. Therefore, detailed analysis of the families with DS is needed to find out other possible causative factors for nondisjunction.

Methods

We investigated 69 families of cytogenetically confirmed DS children and constructed pedigrees of these families. We also studied 200 randomly selected families belonging to different religions as controls. Statistical analysis was carried out using logistic regression.

Results

Out of the 69 DS cases studied, 67 were free trisomy 21, two cases were mosaic trisomy 21 and there were none with translocation. The number of DS births was greater for the young age mothers compared with the advanced age mothers. It has also been recorded that young age mothers (18 to 29 years) born to their mothers at the age 30 years and above produced as high as 91.3% of children with DS. The logistic regression of case- control study of DS children revealed that the odds ratio of age of grandmother was significant when all the four variables were used once at a time. However, the effect of age of mother and father was smaller than the effect of age of maternal grandmother. Therefore, for every year of advancement of age of the maternal grandmother, the risk (odds) of birth of DS baby increases by 30%.

Conclusion

Besides the known risk factors, mother's age, father's age, the age of the maternal grandmother at the time of birth of the mother is a risk factor for the occurrence of Down syndrome.
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Literature
1.
go back to reference Lamb NE, Feingold E, Savage A, Avramopoulos D, Freeman S, Gu Y, Hallberg A, Hersey J, Karadima G, Pettay D, Saker D, Shen J, Taft L, Millelsen M, Petersen MB, Hassold T, Sherman SL: Characterization of susceptible chaisma configuration that increases the risk for maternal non-disjunction of chromosome 21. Human Molecular Genetics. 1997, 6: 1391-1399. 10.1093/hmg/6.9.1391.CrossRefPubMed Lamb NE, Feingold E, Savage A, Avramopoulos D, Freeman S, Gu Y, Hallberg A, Hersey J, Karadima G, Pettay D, Saker D, Shen J, Taft L, Millelsen M, Petersen MB, Hassold T, Sherman SL: Characterization of susceptible chaisma configuration that increases the risk for maternal non-disjunction of chromosome 21. Human Molecular Genetics. 1997, 6: 1391-1399. 10.1093/hmg/6.9.1391.CrossRefPubMed
2.
go back to reference James SJ, Pogribna M, Pofribny IP, Melnyk S, Hine RJ, Gibson JB, Yi P, Swenson DH, Wilson VL, Gaylor DW: Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome. American J Cli Nut. 1999, 70 (4): 495-501. James SJ, Pogribna M, Pofribny IP, Melnyk S, Hine RJ, Gibson JB, Yi P, Swenson DH, Wilson VL, Gaylor DW: Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome. American J Cli Nut. 1999, 70 (4): 495-501.
3.
go back to reference Stoll C, Alembik Y, Dott B, Roth MP: Study of DS in 238942 consecutive births. Ann Genet. 1998, 41 (1): 44-51.PubMed Stoll C, Alembik Y, Dott B, Roth MP: Study of DS in 238942 consecutive births. Ann Genet. 1998, 41 (1): 44-51.PubMed
4.
go back to reference Stine GJ: The new Human genetics. 1989, Iowa: Wm.C.Brown Publishers Dubuque Stine GJ: The new Human genetics. 1989, Iowa: Wm.C.Brown Publishers Dubuque
5.
go back to reference Antonarakis SE: 10 years of Genomics, chromosome 21, and Down syndrome. Genomics. 1998, 51 (1): 1-16. 10.1006/geno.1998.5335.CrossRefPubMed Antonarakis SE: 10 years of Genomics, chromosome 21, and Down syndrome. Genomics. 1998, 51 (1): 1-16. 10.1006/geno.1998.5335.CrossRefPubMed
6.
go back to reference Hassold T, Sherman S: DS: Genetic recombination and the origin of the extra chromosome 21. Clin Genet. 2000, 57 (2): 95-100. 10.1034/j.1399-0004.2000.570201.x.CrossRefPubMed Hassold T, Sherman S: DS: Genetic recombination and the origin of the extra chromosome 21. Clin Genet. 2000, 57 (2): 95-100. 10.1034/j.1399-0004.2000.570201.x.CrossRefPubMed
7.
go back to reference Lopez PM, Stone D, Gilmour H: Epidemiology of DS in a Scottish city. Paediatr Perinat Epidemiol. 1995, 9 (3): 331-340.CrossRefPubMed Lopez PM, Stone D, Gilmour H: Epidemiology of DS in a Scottish city. Paediatr Perinat Epidemiol. 1995, 9 (3): 331-340.CrossRefPubMed
8.
go back to reference Johnson Z, Lillis D, Delany V, Hayes C, Dack P: The epidemiology of Down syndrome in four countries in Ireland 1981–1990. J Public Health Med. 1996, 18 (1): 78-86.CrossRefPubMed Johnson Z, Lillis D, Delany V, Hayes C, Dack P: The epidemiology of Down syndrome in four countries in Ireland 1981–1990. J Public Health Med. 1996, 18 (1): 78-86.CrossRefPubMed
9.
go back to reference Olsen CL, Cross PK, Gensburg LT, Hughes JP: The effects of prenatal diagnosis, population ageing and changing fertility rates on the live birth prevalence of DS in New York state, 1983–1992. Prenat Diagn. 1996, 16 (11): 991-1002. 10.1002/(SICI)1097-0223(199611)16:11<991::AID-PD977>3.0.CO;2-5.CrossRefPubMed Olsen CL, Cross PK, Gensburg LT, Hughes JP: The effects of prenatal diagnosis, population ageing and changing fertility rates on the live birth prevalence of DS in New York state, 1983–1992. Prenat Diagn. 1996, 16 (11): 991-1002. 10.1002/(SICI)1097-0223(199611)16:11<991::AID-PD977>3.0.CO;2-5.CrossRefPubMed
10.
go back to reference Rosch C, Steinbicker V, Krop S: The effect of prenatal diagnosis and demographic factors in a region of the Eastern part of Germany. Eur J Epidemiol. 2000, 16 (7): 627-32. 10.1023/A:1007693025935.CrossRefPubMed Rosch C, Steinbicker V, Krop S: The effect of prenatal diagnosis and demographic factors in a region of the Eastern part of Germany. Eur J Epidemiol. 2000, 16 (7): 627-32. 10.1023/A:1007693025935.CrossRefPubMed
11.
go back to reference Forrester MB, Merz RD: Epidemiology of DS (trisomy 21), Hawaii 1986–97. Teratology. 2002, 65 (5): 207-312. 10.1002/tera.10042.CrossRefPubMed Forrester MB, Merz RD: Epidemiology of DS (trisomy 21), Hawaii 1986–97. Teratology. 2002, 65 (5): 207-312. 10.1002/tera.10042.CrossRefPubMed
12.
go back to reference Cooley WC, Graham JM: Down Syndrome: An update and review for the primary physician. Clin Pediatr. 1991, 30: 223- Cooley WC, Graham JM: Down Syndrome: An update and review for the primary physician. Clin Pediatr. 1991, 30: 223-
13.
go back to reference Hassold TJ, Hunt P: To err (meiotically) is human: the genesis of human anuploidy. Nature Reviews in Genetics. 2001, 2: 280-291. 10.1038/35066065.CrossRefPubMed Hassold TJ, Hunt P: To err (meiotically) is human: the genesis of human anuploidy. Nature Reviews in Genetics. 2001, 2: 280-291. 10.1038/35066065.CrossRefPubMed
14.
go back to reference Ghosh S, Dey SK: DNA diagnosis of DS using polymerase chain reaction and polymorphic microsatellite markers. Int J Hum Genetics. 2003, 10 (3): 17-20. Ghosh S, Dey SK: DNA diagnosis of DS using polymerase chain reaction and polymorphic microsatellite markers. Int J Hum Genetics. 2003, 10 (3): 17-20.
15.
go back to reference Isaac GS, Krishnamurthy PS, Reddy YR: DS in Hyderabad, India. Acta anthropogenet. 1985, 9 (4): 256-260.PubMed Isaac GS, Krishnamurthy PS, Reddy YR: DS in Hyderabad, India. Acta anthropogenet. 1985, 9 (4): 256-260.PubMed
16.
go back to reference Verma IC, Anand NK, Kabra M, Menon PSN, Sharma N: Study of malformations and DS in India (SOMDI): Delhi region. Ind J Hum Genet. 1998, 4: 84-87. Verma IC, Anand NK, Kabra M, Menon PSN, Sharma N: Study of malformations and DS in India (SOMDI): Delhi region. Ind J Hum Genet. 1998, 4: 84-87.
17.
go back to reference Modi UJ, Nayak U, Aiyer S, Bharani S, Master DC, Shah T, Anerao M: Study of Malformations and DS in India (SOMDI): Baroda Region. Ind J Hum Genet. 1998, 4: 93-98. Modi UJ, Nayak U, Aiyer S, Bharani S, Master DC, Shah T, Anerao M: Study of Malformations and DS in India (SOMDI): Baroda Region. Ind J Hum Genet. 1998, 4: 93-98.
18.
go back to reference Jyothy A, Kumar KS, Rao GN, Rao VB, Swarna M, Devi BU, Sujatha M, Kumari CK, Reddy PP: Cytogenetic studies of 1001 Down syndrome cases from Andra Pradesh, India. Indian J Med Res. 2000, 111: 133-137.PubMed Jyothy A, Kumar KS, Rao GN, Rao VB, Swarna M, Devi BU, Sujatha M, Kumari CK, Reddy PP: Cytogenetic studies of 1001 Down syndrome cases from Andra Pradesh, India. Indian J Med Res. 2000, 111: 133-137.PubMed
19.
go back to reference Kothare S, Shetty N, Dave U: Maternal age and chromosomal profile in 160 DS cases-Experience of tertiary genetic center from India. Int J Hum Genetics. 2002, 2 (1): 49-53. Kothare S, Shetty N, Dave U: Maternal age and chromosomal profile in 160 DS cases-Experience of tertiary genetic center from India. Int J Hum Genetics. 2002, 2 (1): 49-53.
20.
go back to reference Kaur A, Mahajan S, Singh JR: Cytogenetic profile of individual with mental retardation. Int J Hum Genetics. 2003, 3 (1): 13-16. Kaur A, Mahajan S, Singh JR: Cytogenetic profile of individual with mental retardation. Int J Hum Genetics. 2003, 3 (1): 13-16.
21.
go back to reference Rao VB: Mean maternal age of Down's syndrome in Hyderabad, India. J Indian Med Assoc. 1999, 97 (1): 25-PubMed Rao VB: Mean maternal age of Down's syndrome in Hyderabad, India. J Indian Med Assoc. 1999, 97 (1): 25-PubMed
22.
go back to reference Jyothy A, Kumar KS, Mallikarjuna GN, Rao VB, Devi BU, Sujatha M, Reddy PP: Parental age and the origin of extra chromosome 21 in DS. J Hum Genet. 2001, 46: 347-350. 10.1007/s100380170071.CrossRefPubMed Jyothy A, Kumar KS, Mallikarjuna GN, Rao VB, Devi BU, Sujatha M, Reddy PP: Parental age and the origin of extra chromosome 21 in DS. J Hum Genet. 2001, 46: 347-350. 10.1007/s100380170071.CrossRefPubMed
23.
go back to reference Bittles AH, Glasson EJ: Clinical, social, and ethical implications of changing life expectancy in Down syndrome. Dev Med Child Neurol. 2004, 46: 282-85.CrossRefPubMed Bittles AH, Glasson EJ: Clinical, social, and ethical implications of changing life expectancy in Down syndrome. Dev Med Child Neurol. 2004, 46: 282-85.CrossRefPubMed
24.
go back to reference Patterson D, Costa AC: Down syndrome and genetics- a case of linked histories. Nature Review Genetics. 6: 137-147. 10.1038/nrg1525. Patterson D, Costa AC: Down syndrome and genetics- a case of linked histories. Nature Review Genetics. 6: 137-147. 10.1038/nrg1525.
25.
go back to reference Sayee R, Thomas IM: DS with unusual familial translocation (1:21): A case report. Indian J Pediatr. 1996, 63 (1): 121-126.CrossRef Sayee R, Thomas IM: DS with unusual familial translocation (1:21): A case report. Indian J Pediatr. 1996, 63 (1): 121-126.CrossRef
26.
go back to reference Jyothy A, Rao GN, Kumar KS, Rao VB, Devi BU, Reddy PP: Translocation DS. Indian J Med Sci. 2002, 56 (5): 225-229.PubMed Jyothy A, Rao GN, Kumar KS, Rao VB, Devi BU, Reddy PP: Translocation DS. Indian J Med Sci. 2002, 56 (5): 225-229.PubMed
27.
go back to reference Aagesen L, Grinsted J, Mikkelsen M: Advanced grandmaternal age on the mother's side- a risk of giving rise to trisomy 21. Ann hum Genet. 1984, 48: 297-302.CrossRefPubMed Aagesen L, Grinsted J, Mikkelsen M: Advanced grandmaternal age on the mother's side- a risk of giving rise to trisomy 21. Ann hum Genet. 1984, 48: 297-302.CrossRefPubMed
28.
go back to reference Mikkelsen M: Down anomaly: New research of an old and well known syndrome. Medical genetics: Past, Present, Future. Edited by: Berg K. 1985, New York: Alan R. Liss Mikkelsen M: Down anomaly: New research of an old and well known syndrome. Medical genetics: Past, Present, Future. Edited by: Berg K. 1985, New York: Alan R. Liss
29.
go back to reference Papp Z, Varadi E, Szabo Z: Grandmaternal age at birth of parents of children with trisomy. Hum Genet. 1977, 39: 221-224. 10.1007/BF00287015.CrossRefPubMed Papp Z, Varadi E, Szabo Z: Grandmaternal age at birth of parents of children with trisomy. Hum Genet. 1977, 39: 221-224. 10.1007/BF00287015.CrossRefPubMed
30.
go back to reference Brown AS, Feingold E, Broman KW, Sherman SL: Genome wide variation in recombination in female meiosis: A risk factor for no disjunction of chromosome 21. Human Molecular Genetics. 2000, 9 (4): 515-523. 10.1093/hmg/9.4.515.CrossRefPubMed Brown AS, Feingold E, Broman KW, Sherman SL: Genome wide variation in recombination in female meiosis: A risk factor for no disjunction of chromosome 21. Human Molecular Genetics. 2000, 9 (4): 515-523. 10.1093/hmg/9.4.515.CrossRefPubMed
31.
go back to reference Jeffreys CA, Burrage PS, Bickel SE: A model system for increased meiotic nondisjunction in older oocytes. Curr Biol. 2003, 13: 498-503. 10.1016/S0960-9822(03)00134-9.CrossRefPubMed Jeffreys CA, Burrage PS, Bickel SE: A model system for increased meiotic nondisjunction in older oocytes. Curr Biol. 2003, 13: 498-503. 10.1016/S0960-9822(03)00134-9.CrossRefPubMed
32.
go back to reference Gardiner K, Slavov D, Bechtel L, Davisson M: Annotation of human chromosome 21 for relevance to DS: Gene structure and expression analysis. Genomics. 2002, 79 (6): 833-844. 10.1006/geno.2002.6782.CrossRefPubMed Gardiner K, Slavov D, Bechtel L, Davisson M: Annotation of human chromosome 21 for relevance to DS: Gene structure and expression analysis. Genomics. 2002, 79 (6): 833-844. 10.1006/geno.2002.6782.CrossRefPubMed
Metadata
Title
Influence of advanced age of maternal grandmothers on Down syndrome
Authors
Suttur S Malini
Nallur B Ramachandra
Publication date
01-12-2006
Publisher
BioMed Central
Published in
BMC Medical Genetics / Issue 1/2006
Electronic ISSN: 1471-2350
DOI
https://doi.org/10.1186/1471-2350-7-4

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