BMJ 1994;309:570-573 (3 September)

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Case-control study of whether subfertility in men is familial

R Lilford, A M Jones, D T Bishop, J Thornton, R Mueller 

Institute of Edpidemiology and Health Services Research, Department of Clinical Medicine, University of Leeds, Leeds LS2 9LN Correspondence to: Professor Lilford.

Abstract

Objective : To test the hypothesis that subfertility in men is familial and to examine the distribution of subfertility within families for consistency with a genetic cause.
Design : Case-control study and segregation analysis.
Setting : Two teaching hospitals in Leeds.
Subjects : Cases (probands) were men with an abnormal sperm count who attended a subfertility clinic and whose partners had no major factor contravening fertility. Controls were fathers of two or more children recruited through vasectomy clinics or a maternity department.
Main outcome measures : The incidence of involuntary20childlessness among brothers with partners and among sisters and second and third degree male relatives. When possible clinical and laboratory details were obtained from involuntarily childless brothers.
Results : Seventeen of the 148 (11.5%) brothers of probands but none of the 169 brothers of controls had sought medical advice for childlessness (P<0.0005). Four probands had more than one involuntarily childless brother. There were six further brothers whose childlessness was thought to be involuntary bringing the total prevalence of subfertility among brothers of probands to 16%. Segregation analysis was consistent with an autosomal recessive mode of inheritance accounting for 60% of subfertility in men. Seventeen of the 346 (4.9%) uncles of probands and 10 of 420 (2.8%) uncles of controls were reported to be involuntarily childless (P=0.09), but there was no difference in childlessness among sisters. In three families sperm counts from "affected" brothers confirmed the diagnosis and showed considerable similarities within but not between families.
Conclusion : Subfertility in men has a familial component, and the observations are consistent with an autosomal recessive mode of inheritance in over half the cases. Several different genes are probably involved.

Clinical implications

  • Clinical implications

  • Subfertility in men is not often caused by chromosome abnormalities

  • A common genetic mechanism for subfertility in men is not implausible as human survival is not dependent on maximising the number of offspring and many autosomal recessive conditions are lethal before the individual reaches maturity

  • A higher proportion of brothers (with partners) of men treated for subfertility were involuntarily childless compared with brothers of men with at least two children

  • Segregation analysis was consistent with an autosomal recessive mode of inheritance accounting for 60% of subfertility in men


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Relevant Article

Subfertility in men Measurement error and confounding not accounted for
D Gregson, E Smyth, J Flowers, F J Steward, A J Hill, and R J Lilford
BMJ 1994 309: 1085-1086. [Extract] [Full Text]

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