Literature DB >> 33706792

Smoking and alcohol, health-related quality of life and psychiatric comorbidities in Leber's Hereditary Optic Neuropathy mutation carriers: a prospective cohort study.

Andrea Rabenstein1, Claudia B Catarino2, Tobias Rüther3, Thomas Klopstock4,5,6, Verena Rampeltshammer3, David Schindler3, Constanze Gallenmüller2, Claudia Priglinger7, Oliver Pogarell3.   

Abstract

BACKGROUND: Leber's hereditary optic neuropathy (LHON) is a rare mitochondrial disorder, characterized by acute or subacute bilateral vision loss, frequently leading to significant chronic disability, mainly in young people. The causal LHON mutations of the mitochondrial DNA have incomplete penetrance, with the highest risk of disease manifestation for male mutation carriers in the second and third decades of life. Here we evaluated smoking, alcohol drinking habits, health-related quality of life (QOL) and psychiatric comorbidities in a cohort of LHON patients and asymptomatic mutation carriers from a tertiary referral centre.
METHODS: Cross-sectional analysis of the ongoing Munich LHON prospective cohort study. Participants included all LHON patients and asymptomatic LHON mutation carriers older than 16 years at baseline, who were recruited between February 2014 and June 2015 and consented to participate. General, neurological and ophthalmological investigations were performed, including validated questionnaires on smoking, alcohol drinking habits, depressive symptoms and health-related QOL.
RESULTS: Seventy-one participants were included, 34 LHON patients (82% male) and 37 asymptomatic mutation carriers (19% male). Median age at baseline was 36 years (range 18-75 years). For LHON patients, median age at visual loss onset was 27 years (9 to 72 years). Smoking is more frequent in LHON patients than asymptomatic LHON mutation carriers, and significantly more frequent in both groups than in the general population. Sixty percent of LHON patients, who smoked at disease onset, stopped or significantly reduced smoking after visual loss onset, yet 40% of LHON patients continued to smoke at study baseline. Excessive alcohol consumption is more frequent in male LHON patients than in LHON asymptomatic and more frequent than in the male general population. Further, female asymptomatic LHON mutation carriers are at risk for depression and worse mental QOL scores.
CONCLUSIONS: Given the high prevalence of smoking and excessive drinking in LHON mutation carriers, implementing effective measures to reduce these risk factors may have a significant impact in reducing LHON disease conversion risk. The underrecognized prevalence of mental health issues in this population of LHON mutation carriers highlights the need for awareness and more timely diagnosis, which may lead to improved outcomes.

Entities:  

Keywords:  Alcohol; Depression; LHON; Leber’s hereditary optic atrophy; Mental health (< 10); Mitochondrial disorder; Quality of life; Smoking

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Substances:

Year:  2021        PMID: 33706792      PMCID: PMC7953635          DOI: 10.1186/s13023-021-01724-5

Source DB:  PubMed          Journal:  Orphanet J Rare Dis        ISSN: 1750-1172            Impact factor:   4.123


  2 in total

1.  Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.

Authors:  N Howell; L A Bindoff; D A McCullough; I Kubacka; J Poulton; D Mackey; L Taylor; D M Turnbull
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

2.  Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy.

Authors:  Annalinda Pisano; Carmela Preziuso; Luisa Iommarini; Elena Perli; Paola Grazioli; Antonio F Campese; Alessandra Maresca; Monica Montopoli; Laura Masuelli; Alfredo A Sadun; Giulia d'Amati; Valerio Carelli; Anna Ghelli; Carla Giordano
Journal:  Hum Mol Genet       Date:  2015-09-26       Impact factor: 6.150

  2 in total
  4 in total

1.  Risk of Burning Mouth Syndrome in Patients with Migraine: A Nationwide Cohort Study.

Authors:  Dong-Kyu Kim; Hyun-Joo Lee; Il Hwan Lee; Jae-Jun Lee
Journal:  J Pers Med       Date:  2022-04-11

2.  Prevalence of primary mutations in Leber hereditary optic neuropathy: A five-year report from a tertiary eye care center in India.

Authors:  Srilekha Sundaramurthy; Ambika Selvakumar; Vidhya Dharani; Nagasamy Soumittra; Jayaprakash Mani; Karthiyayini Thirumalai; Porkodi Periyasamy; Sinnakaruppan Mathavan; Sarangapani Sripriya
Journal:  Mol Vis       Date:  2021-12-11       Impact factor: 2.367

3.  Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study.

Authors:  Julia Zibold; Bettina von Livonius; Hana Kolarova; Günter Rudolph; Claudia S Priglinger; Thomas Klopstock; Claudia B Catarino
Journal:  Orphanet J Rare Dis       Date:  2022-08-09       Impact factor: 4.303

Review 4.  Mitochondrial Disorders.

Authors:  Thomas Klopstock; Claudia Priglinger; Ali Yilmaz; Cornelia Kornblum; Felix Distelmaier; Holger Prokisch
Journal:  Dtsch Arztebl Int       Date:  2021-11-05       Impact factor: 8.251

  4 in total

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