|
|
| Research article summary (published 19 Oct 2009): |
Implications of hypertrophic cardiomyopathy transmitted by sperm donation.
Full Abstract
CONTEXT: Sperm donation is an increasingly common practice for achieving pregnancy in the absence of a male partner or when fertility is problematic. The unintended consequence in which genetic diseases are unwittingly transmitted to offspring is an underrecognized public health issue not previously prioritized by US Food and Drug Administration guidelines. OBJECTIVE: To report the clinical circumstances and implication of hypertrophic cardiomyopathy (HCM) transmitted by sperm donation to recipients. SETTING: Voluntary sperm donation through a US Food and Drug Administration-approved tissue bank. MAIN OUTCOME MEASURE: Incidence of genetically affected offspring and clinical outcomes to date. RESULTS: An asymptomatic 23-year-old man who had no personal knowledge of underlying heart disease and who underwent standard testing that was negative for infectious diseases, repeatedly donated sperm over a 2-year period (1990-1991). The donor was later shown to be affected (in 2005) by a novel beta-myosin heavy-chain mutation that caused HCM, after an offspring was clinically diagnosed with this disease. Of the 24 children known to be offspring of the donor, including 22 who were products of fertilization via sperm donation and 2 conceived by the donor's wife, a total of 9 genetically affected offspring, 2 to 16 years of age and 6 males, have been identified with HCM (2005-2009). Three of the 9 gene-positive children have currently expressed phenotypic evidence of HCM, including one who died at age 2 years due to progressive and unrelenting heart failure with marked hypertrophy, and also 2 survivors with extreme left ventricular hypertrophy at age 15 years. The latter 2 children and the donor are judged likely to be at increased risk for sudden death. CONCLUSIONS: This case series underscores the potential risk for transmission of inherited cardiovascular diseases through voluntary sperm donation, a problem largely unappreciated by the medical community and agencies regulating tissue donation. Recommendations include improved screening guidelines for donors to exclude cardiovascular diseases (eg, HCM) such as consideration for 12-lead electrocardiograms.
Author information
Author/s: Maron, Barry J (BJ); Lesser, John R (JR); Schiller, Nelson B (NB); Harris, Kevin M (KM); Brown, Colleen (C); Rehm, Heidi L (HL);
Affiliation: Hypertrophic Cardiomyopathy Center, Minneapolis Heart Institute Foundation and Abbott Northwestern Hospital, Minneapolis, Minnesota 55407, USA. hcm.maron(-atsign-)mhif.org
Journal and publication information
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
Journal: JAMA : the journal of the American Medical Association (JAMA), published in United States. (Language: eng)
Reference: 2009-Oct; vol 302 (issue 15) : pp 1681-4
Dates: Created 2009/10/21; Completed 2009/11/02; Revised 2009/11/13;
PMID: 19843903, status: MEDLINE (last retrieval date: 11/15/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
Comments and Corrections
CommentIn: JAMA. 2009 Oct 21;302(15):1702-4. (PMID: 19843908)
ErratumIn: JAMA. 2009 Nov 11;302(18):1972.
External Links for this article
(including full text providers, if available):
Click Electronic Full-text Provider Links to see options for finding the electronic full text links to this article. Note there may be a subscription or fee required for access to the full text. See our FAQ for information on finding FREE full text articles.
This article may also be located in paper journal collections available in many libraries. Use the Journal and Publication Information above to find the full article.
MeSH headings (categories)
This article was linked to the MESH Headings shown below.
Related articles
These are the highest related articles currently in the database:
- A PCR-based integrated protocol for the structural analysis of the 13th exon of the human beta-myosin heavy chain gene (MYH7): development of a diagnostic tool for HCM disease.
14 Apr 2008 - [Hypertrophic cardiomyopathy: infrequent mutation of the cardiac beta-myosin heavy-chain gene]
30 Jul 2006 - [Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy]
29 Sep 2006 - As the use of donor sperm increases, secrecy can be a health hazard.
4 Jun 2006 - Genotype-phenotype correlation of R870H mutation in hypertrophic cardiomyopathy.
29 Apr 2006 - Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene.
30 Aug 1999 - Array-based resequencing assay for mutations causing hypertrophic cardiomyopathy.
5 Feb 2008 - Gene symbol: MYH7. Disease: cardiomyopathy, hypertrophic.
29 Nov 2005 - Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation.
21 Mar 2007 - Long-term follow-up of R403WMYH7 and R92WTNNT2 HCM families: mutations determine left ventricular dimensions but not wall thickness during disease progression.
29 Apr 2007
Related Article Map
Legend:
- FREE Full text Article.
- Abstract only.
- Title only. More help.
See a large map of 100+ related articles.