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,
From the * Andrology and IVF Laboratories,
Department of Surgery, the
Department of
Physiology, and the
Department of Obstetrics
and Gynecology, University of Utah School of Medicine, Salt Lake City,
Utah
| Correspondence to: Douglas T. Carrell, Andrology and IVF Laboratories, University of Utah School of Medicine, 675 Arapeen Drive, Ste 205, Salt Lake City, UT 84117 (e-mail: douglas.carrell{at}hsc.utah.edu). |
Male infertility affects a large proportion of the population. In spite of
the magnitude of the problem and the considerable research effort that has
been made to understand its causes, a large proportion of male infertility
cases remain idiopathic in nature. This pilot genome-wide association study
employed genotyping microarray technology to interrogate over 370 000
single-nucleotide polymorphisms (SNPs) in men with azoospermia and severe
oligozoospermia, along with normozoospermic controls, in an effort to discover
novel genetic variants significantly associated with male infertility. We
found 20 SNPs significantly associated with azoospermia or oligozoospermia
(P value for association of <1 x 10–5).
Using a gene-centric approach evaluating SNPs associated with genes of known
fertility function, we found 1 additional SNP with P < 1 x
10–4. Although additional studies with larger numbers of
samples will be required to validate these results and to identify causal
variants, this study represents an important first step in applying
genome-wide approaches to identify the genetic causes of male infertility.
Key words: Genetic variation, mutation, genome-wide association study, infertility, microarray
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