Birth order pattern in the inheritance of chronic lymphocytic leukaemia and related lymphoproliferative disease

Leukemia and Lymphoma

Volumn 48, Issue 12, 2007, Pages 2387-2396

  Jønsson, Viggo ^a   Tjønnfjord, Geir ^b   Samuelsen, Sven Ove ^b   Johannesen, Tom ^c   Olsen, Jørgen ^d   Sellick, Gabrielle ^e   Houlston, Richard ^e   Yuille, Martin ^f   Catovsky, Daniel ^e  

^a AKER UNIVERSITY HOSPITAL   (Norway)

^b UNIVERSITY OF OSLO   (Norway)

^c CANCER REGISTRY OF NORWAY   (Norway)

^d Danish Cancer Registry   (Denmark)

^e INSTITUTE OF CANCER RESEARCH   (United Kingdom)

^f DNA Banking Network   (United Kingdom)

Author keywords

Birth order effect; Chronic lymphocytic leukaemia; Imprinting; Lymphoproliferative disorders; Microchimerism; Non Hodgkin's lymphoma

Indexed keywords

ARTICLE; BIRTH ORDER; CANCER RISK; CHRONIC LYMPHATIC LEUKEMIA; CLINICAL ARTICLE; EPIGENETICS; EXTRACHROMOSOMAL INHERITANCE; FEMALE; GENETIC PREDISPOSITION; GENOME IMPRINTING; HERITABILITY; HUMAN; LYMPHOPROLIFERATIVE DISEASE; MALE; MICROCHIMERISM; PEDIGREE ANALYSIS; PRIORITY JOURNAL; PROPORTIONAL HAZARDS MODEL; RISK FACTOR;

ADULT; AGED; BIRTH ORDER; EPIGENESIS, GENETIC; FEMALE; GENOMIC IMPRINTING; HUMANS; LEUKEMIA, LYMPHOCYTIC, CHRONIC, B-CELL; LYMPHOPROLIFERATIVE DISORDERS; MALE; MIDDLE AGED; REGRESSION ANALYSIS;

EID: 37149024085     PISSN: 10428194     EISSN: 10292403     Source Type: Journal    
DOI: 10.1080/10428190701686273     Document Type: Article

References (41)

1. Houlston, R. S., Sellick, G., Yuille, M., Matutes, E. and Catovsky, D. (2003) Causation of chronic lymphocytic leukaemia - insight from familial disease. Leuk Res, 27, pp. 871-876.
2. Goldin, L. R., Pfeiffer, R. M., Li, X. and Hemminki, K. (2004) Familial risk of lymphoproliferative tumors in families of patients with chronic lymphocytic leukemia, results from the Swedish family-cancer database. Blood, 194, pp. 1850-1854.
3. Daugherty, S. E., Pfeiffer, R. M., Mellemkjaer, L. and Hemminki, K. (2005) No evidence for anticipation in lymphoproliferative tumors in population-based samples. Cancer Epidemiol Biomarkers Prev, 14, pp. 1245-1250.
4. Alexandrescu, D. T., Garino, A., Brown-Balem, K. A. and Wiernik, P. H. (2006) Anticipation in families with Hodgkin's and non-Hodgkin's lymphoma in their pedigree. Leuk Lymph, 47, pp. 2115-2127.
5. Goldin, L. R., Ishibe, N., Sgambati, M., Marti, G. E., Fontaine, L. and Lee, M. P. (2003) A genome scan of 18 families with chronic lymphocytic leukaemia. Br J Haematol, 121, pp. 866-873.
6. Segel, G. B. and Lichtman, M. A. (2004) Familial inherited leukemia, lymphoma, and myeloma, an overview. Blood Cells Mol Dis, 32, pp. 246-261.
7. Sellick, G. S., Webb, E. L., Allinson, R., Matutes, E., Dyer, M JS and Jønsson, V. (2005) A high-density SNP genomewide linkage scan for chronic lymphocytic leukemia-susceptibility loci. Am J Hum Genet, 77, pp. 420-429.
8. Hartwell, L. H., Hood, L., Goldberg, M. L., Reynolds, A. E., Silver, L. M. and Veres, R. C. (2000) Genomic imprinting. Genetics from genes to genomes, pp. 408-410. McGraw Hill, Boston
9. Angiolini, E., Fowden, A., Coan, P., Sandovici, I., Smith, P. and Dean, W. (2006) Regulation of placental efficiency for nutrient transport by imprinted genes. Placenta, 27, pp. 98-102.
10. Federman, D. D. (2006) The biology of human sex differences. N Engl J Med, 354, pp. 1507-1517.
11. Kaneko-Ishino, T., Kohda, T., Ono, R. and Ishino, F. (2006) Complementation hypothesis, the necessity of a monoallelic gene expression mechanism in mammalian development. Cytogen Genom Res, 113, pp. 24-30.
12. Lewis, A. and Reik, W. (2006) How imprinting centres work. Cytogen Genom Res, 113, pp. 81-89.
13. Santure, A. W. and Spencer, H. G. (2006) Influence of mom and dad, quantitative genetic models for maternal effects on genomic imprinting. Genetics, 173, pp. 2297-2316.
14. Wilkins, J. F. (2006) Competative signal discrimination, methylation, reprogramming and genomic imprinting. J Theoret Biol, 242, pp. 643-651.
15. Emery, A EH (1986) Parental age and birth order. Methodology in medical genetics, pp. 140-153. Churchill Livingstone, Edinburgh, London
16. Moore, T. and Haig, D. (1991) Genomic imprinting in mammalian development, a parental tug-of-war. Trends Genet, 7, pp. 45-49.
17. Ong, K. K., Petry, C. J., Barratt, B. J., Ring, S., Cordell, H. J., Wingate, D. L. and the Avon Longitudinal Study of Pregnancy and Childhood Study Team (2004) Maternal-fetal interaction and birth order influence insulin variable number of tandem repeats allele class associations with head size at birth and childhood weight gain. Diabetes, 53, pp. 1128-1133.
18. Harris, N. L. and Ferry, J. A. (2001) Classification of non-Hodgkin's lymphomas. Neoplastic Hematopathology, pp. 691-753. Lippincott Williams & Wilkins, Philadelphia
19. Muller-Hermelink, H. K., Catovsky, D., Montserrat, E. and Harris, N. L. (2001) Chronic lymphocytic leukemia/small lymphocytic lymphoma. Tumours of Haematopoietic and Lymphoid Tissues, pp. 127-130. IARC Press, Lyon
20. Chiorazzi, N., Rai, K. R. and Ferrarini, M. (2005) Chronic lymphocytic leukemia. N Engl J Med, 352, pp. 804-815.
21. Cox, D. R. (1958) The regression analysis of binary sequences. J R Stat Soc, 20, pp. 215-242.
22. Haldane, J BS and Smith, C AB (1947) A simple exact test for birth-order effect. Ann Eugenics, 14, pp. 117-124.
23. Wilcoxon, F. (1947) Probability tables for individual comparisons by ranking methods. Biometrics, 3, pp. 119-122.
24. Rawstron, A. C., Yuille, M. R., Fuller, J., Cullen, M., Kennedy, B. and Richards, S. J. (2002) Inherited predisposition to CLL is detectable as subclinical monoclonal B-lymphocyte expansion. Blood, 100, pp. 2289-2290.
25. Kyle, R. A., Terneau, T. M., Rajkumar, S. V., Offord, J. R., Larson, D. R. and Plevak, M. F. (2002) A long-term study of prognosis in monoclonal gammopathy of undetermined significance. N Engl J Med, 346, pp. 564-569.
26. Isaacson, P. G. (2001) Gastrointestinal lymphomas and lymphoid hyperplasias. Neoplastic Hematopathology, pp. 1235-1261. Lippincott Williams & Wilkins, Philadelphia
27. Birth statistics in Denmark National Board of Health, Vital Statistics I Birth Register, 2007, State Publ. Denmark, Copenhagen
28. Irgens, L. M. The medical birth registry in Norway. Epidemiological research and surveillance throughout 30 years. Acta Obstet Gynecol Scand, 79, pp. 435-439.
29. Skjaerven, R., Vatten, L. J., Wilcox, A. J., Rønning, T., Irgens, L. M. and Lie, R. T. Recurrence of pre-eclapsia across generations, exploring fetal and maternal genetic components in a population based cohort. BMJ
30. Altieri, A., Castro, F., Bermejo, J. L. and Hemminki, K. (2006) Number of siblings and risk of lymphoma, leukemia and myeloma by histopathology. Cancer Epidemiol Biomarkers Prev, 15, pp. 1281-1286.
31. Wang, S. S., Slanger, S. L., Brennan, P., Holly, E. A., De Sanjose, S. and Bernstein, L. (2007) Family history of hemotopoietic malignancies and risk of non-Hodgkin lymphoma (NHL), a pooled analysis of 10211 cases and 11905 controls from the International Lymphoma Epidemiology Consortium (InterLymph). Blood, 109, pp. 3479-3488.
32. Smith, C AB (1958) Discussion on Dr. Cox's paper. The regression analysis of binary sequences, 20, pp. 232-233.
33. Nelson, J. L. (1998) Microchimerism and autoimmune disease. N Engl J Med, 338, pp. 1224-1225.
34. Adams, K. M. and Nelson, J. L. (2004) Microchimerism: An investigative frontier in autoimmunity and transplantation. JAMA, 291, pp. 1127-1131.
35. Adams, K. M. and Gadi, V. K. (2006) Autoimmunity in CLL, grave consequences of gravidity?. Leuk Lymph, 47, pp. 1445-1446.
36. Stevens, A. M., McDonnell, W. M., Mullarkey, M. E., Pang, J. M., Leisenring, W. and Nelson, J. L. (2004) Liver biopsies from human females contain male hepatocytes in the absence of transplantation. Lab Invest, 84, pp. 1603-1609.
37. Bayes-Genis, A., Bellosillo, B., de la Calle, O., Salido, M., Roura, S. and Ristol, F. S. (2005) Identification of male cardiomyocytes of extracardiac origin in the hearts of woman with male progeny, male fetal cell microchimerism in the heart. J Heart Lung Transplant, 24, pp. 2179-2183.
38. Ubeda, F. and Haig, D. (2005) On the evolutionary stability of Mendelian segregation. Genetics, 170, pp. 1345-1357.
39. Raval, A., Byrd, J. C. and Plass, C. (2006) Epigenetics in chronic lymphocytic leukemia. Semin Oncol, 33, pp. 157-166.
40. Raval, A., Tanner, S. M., Bryd, J. C., Angerman, E. B., Perko, J. D. and Chen, S. S. (2007) Downregulation of death-associated protein kinase 1 (DAPK 1) in chronic lymphocytic leukemia. Cell, 129, pp. 879-890.
41. Amiel, A., Leopold, L., Gronich, N., Yukla, M., Fejgin, M. D. and Lishner, M. (2006) The influence of different chromosomal aberrations on molecular cytogenetic parameters in chronic lymphocytic leukemia. Cancer Genet Cytogenet, 167, pp. 145-149.