Mutation in the mitochondrial tRNA(leu) at position 3243 and spontaneous abortions in Japanese women attending a clinic for diabetic pregnancies
- PMID: 7556983
- DOI: 10.1007/s001250050357
Mutation in the mitochondrial tRNA(leu) at position 3243 and spontaneous abortions in Japanese women attending a clinic for diabetic pregnancies
Abstract
Mitochondrial DNA is exclusively maternally inherited. We recently found the prevalence of diabetic patients with an A to G transition at position 3243 of leucine tRNA (3243 base pair (bp) mutation) to be nearly 1% in randomly selected Japanese subjects. Here, we report the higher prevalence of diabetic patients with the 3243 bp mutation in a specific Japanese population of women attending a diabetic pregnancy clinic. Of 102 patients with non-insulin-dependent diabetes mellitus 6 (5.9%) were positive for the mutation, 1 (8.3%) of 12 patients with gestational diabetes and 2 (5.9%) out of 34 borderline diabetic patients. In contrast, none of 64 patients (0%) with insulin-dependent diabetes mellitus had the 3243 bp mutation. Moreover, there was a difference in the prevalence of spontaneous abortions between patients with and without this mutation (27.3 vs 12.4%). Among nine probands with the mutation, four had a history of one spontaneous abortion (p = 0.0518) and two had a history of two abortions (p = 0.0479). Two probands had a spontaneous abortion even while under strict diabetic metabolic control. The 3243 bp mutation thus may cause spontaneous abortion during pregnancy.
Similar articles
-
Beta-cell loss and glucose induced signalling defects in diabetes mellitus caused by mitochondrial tRNALeu(UUR) gene mutation.Diabet Med. 1996 Sep;13(9 Suppl 6):S98-102. Diabet Med. 1996. PMID: 8894492
-
Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.Diabetologia. 1994 May;37(5):504-10. doi: 10.1007/s001250050139. Diabetologia. 1994. PMID: 8056189
-
A subtype of diabetes mellitus associated with a mutation in the mitochondrial gene.Muscle Nerve Suppl. 1995;3:S137-41. doi: 10.1002/mus.880181427. Muscle Nerve Suppl. 1995. PMID: 7603515
-
Mitochondrial diabetes mellitus: a review.Biochim Biophys Acta. 1995 May 24;1271(1):253-60. doi: 10.1016/0925-4439(95)00036-4. Biochim Biophys Acta. 1995. PMID: 7599217 Review.
-
The genetics of diabetic pregnancy.Best Pract Res Clin Obstet Gynaecol. 2015 Jan;29(1):102-9. doi: 10.1016/j.bpobgyn.2014.08.008. Epub 2014 Aug 26. Best Pract Res Clin Obstet Gynaecol. 2015. PMID: 25438929 Review.
Cited by
-
Deep sequencing shows that accumulation of potentially pathogenic mtDNA mutations rather than mtDNA copy numbers may be associated with early embryonic loss.J Assist Reprod Genet. 2020 Sep;37(9):2181-2188. doi: 10.1007/s10815-020-01893-5. Epub 2020 Jul 23. J Assist Reprod Genet. 2020. PMID: 32700162 Free PMC article.
-
Maternally inherited diabetes and deafness: a new diabetes subtype.Diabetologia. 1996 Apr;39(4):375-82. doi: 10.1007/BF00400668. Diabetologia. 1996. PMID: 8777986 Review.
-
A retrospective cohort study evaluating pregnancy outcomes in women with MIDD.Acta Diabetol. 2024 Mar;61(3):323-331. doi: 10.1007/s00592-023-02202-z. Epub 2023 Oct 31. Acta Diabetol. 2024. PMID: 37907768
-
Large-scale study of an A-to-G transition at position 3243 of the mitochondrial gene and IDDM in Japanese patients.Diabetologia. 1996 Feb;39(2):245-6. doi: 10.1007/BF00403970. Diabetologia. 1996. PMID: 8635679 No abstract available.
-
Genotypic and phenotypic differences between Arabian and Scandinavian women with gestational diabetes mellitus.Diabetologia. 2004 May;47(5):878-84. doi: 10.1007/s00125-004-1388-5. Epub 2004 Apr 17. Diabetologia. 2004. PMID: 15095040
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical