𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Association of the C677T polymorphism in the methylenetetrahydrofolate reductase gene with sudden sensorineural hearing loss

✍ Scribed by Yasue Uchida; Saiko Sugiura; Fujiko Ando; Hiroshi Shimokata; Tsutomu Nakashima


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
88 KB
Volume
120
Category
Article
ISSN
0023-852X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Objectives/Hypothesis:

To investigate the recently reported association of the C677T polymorphism in the methylenetetrahydrofolate reductase (MTHFR) gene with sudden sensorineural hearing loss (SSNHL), we analyzed data from a community‐based Japanese population.

Study Design:

Nested case‐control study.

Methods:

Among 2,174 adults (1,096 males and 1,078 females) aged 40 to 79 years old who participated in the National Institute for Longevity Sciences–Longitudinal Study of Aging, we compared 33 cases of prevalent SSNHL, defined as a self‐reported otolaryngologist diagnosis, with the other cases. Multiple logistic regression was used to obtain odds ratios (ORs) for SSNHL in subjects with the MTHFR C677T polymorphism, with adjustment for other possibly influential factors under additive, dominant, and recessive genetic models.

Results:

The per‐allele ORs for SSNHL risk were 1.687 (95% confidence interval [CI], 1.023–2.780) in model 1, with adjustment for age and sex, and 1.654 (CI, 1.003–2.728) in model 2, with adjustment for smoking status, body mass index, histories of heart disease, hypertension, and diabetes, in addition to the factors in model 1. In model 3, a significant association between SSNHL and the C677T polymorphism was observed under all genetic models independent of factors including folic acid and homocysteine, although there were only 25 cases and 1,677 controls due to the addition of moderating factors.

Conclusions:

Our results suggest that the T allele of MTHFR C677T could be associated with susceptibility to SSNHL, and even imply that this mutation could be a risk factor that is independent of blood folic acid and homocysteine. Laryngoscope, 2010


πŸ“œ SIMILAR VOLUMES


Association of the C677T and A1298C poly
✍ Ali Sazci; Emel Ergul; Kemal Bayulkem πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 69 KB

## Abstract Essential tremor (ET) is a most common human movement disorder of unknown etiology. Previous reports have shown that the C677T polymorphism of methylenetetrahydrofolate reductase gene has been associated with neurodegenerative disorders. To investigate the role of methylenetetrahydrofol

Distribution of alleles of the methylene
✍ Johnson, William G.; Stenroos, Edward S.; Heath, Simon C.; Chen, Yanping; Carrol πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 28 KB πŸ‘ 2 views

Spina bifida cystica (SB) is one of the most common and disabling of birth defects. Folic acid supplementation in mothers during the periconceptional period has been shown to prevent more than 70% of neural tube defects (NTD) including SB. However, the mechanism is unknown. We tested a series of mul

The relationship of the methylenetetrahy
✍ Z. Eroglu; M. Erdogan; A. Tetik; M. Karadeniz; S. Cetinalp; B. Kosova; C. Gunduz πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 80 KB πŸ‘ 1 views

## Abstract ## Background Poor glycaemic control, hypertension and duration of diabetes are risk factors for the development of diabetic nephropathy, but there may be genetic factors. Recently, a common C to T mutation at nucleotide position 677 of the MTHFR gene (MTHFR677C > T) has been reported