METTL23 Variants and Patients With Normal-Tension Glaucoma

IMPORTANCE: This research confirms and further establishes that pathogenic variants in a fourth gene, METTL23, are associated with autosomal dominant normal-tension glaucoma (NTG). OBJECTIVE: To determine the frequency of glaucoma-causing pathogenic variants in the METTL23 gene in a cohort of patien...

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Veröffentlicht in:Archives of ophthalmology (1960) 2024-11, Vol.142 (11), p.1037-1045
Hauptverfasser: Scheetz, Todd. E, Tollefson, Mallory R, Roos, Ben R, Boese, Erin A, Pouw, Andrew E, Stone, Edwin M, Schnieders, Michael J, Fingert, John H
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container_end_page 1045
container_issue 11
container_start_page 1037
container_title Archives of ophthalmology (1960)
container_volume 142
creator Scheetz, Todd. E
Tollefson, Mallory R
Roos, Ben R
Boese, Erin A
Pouw, Andrew E
Stone, Edwin M
Schnieders, Michael J
Fingert, John H
description IMPORTANCE: This research confirms and further establishes that pathogenic variants in a fourth gene, METTL23, are associated with autosomal dominant normal-tension glaucoma (NTG). OBJECTIVE: To determine the frequency of glaucoma-causing pathogenic variants in the METTL23 gene in a cohort of patients with NTG from Iowa. DESIGN, SETTING, AND PARTICIPANTS: This case-control study took place at a single tertiary care center in Iowa from January 1997 to January 2024, with analysis occurring between January 2023 and January 2024. Two groups of participants were enrolled from the University of Iowa clinics: 331 patients with NTG and 362 control individuals without glaucoma. Patients with a history of trauma; steroid use; stigmata of pigment dispersion syndrome; exfoliation syndrome; or pathogenic variants in MYOC, TBK1, or OPTN were also excluded. MAIN OUTCOMES AND MEASURES: Detection of an enrichment of METTL23 pathogenic variants in individuals with NTG compared with control individuals without glaucoma. RESULTS: The study included 331 patients with NTG (mean [SD] age, 68.0 [11.7] years; 228 [68.9%] female and 103 [31.1%] male) and 362 control individuals without glaucoma (mean [SD] age, 64.5 [12.6] years; 207 [57.2%] female and 155 [42.8%] male). There were 5 detected instances of 4 unique METTL23 pathogenic variants in patients with NTG. Three METTL23 variants—p.Ala7Val, p.Pro22Arg, and p.Arg63Trp—were judged to be likely pathogenic and were detected in 3 patients (0.91%) with NTG. However, when all detected variants were evaluated with either mutation burden analysis or logistic regression, their frequency was not statistically higher in individuals with NTG than in control individuals without glaucoma (1.5% vs 2.5%; P = .27). CONCLUSION AND RELEVANCE: This investigation provides evidence that pathogenic variants in METTL23 are associated with NTG. Within an NTG cohort at a tertiary care center, pathogenic variants were associated with approximately 1% of NTG cases, a frequency similar to that of other known normal-tension glaucoma genes, including optineurin (OPTN), TANK-binding kinase 1 (TBK1), and myocilin (MYOC). The findings suggest that METTL23 pathogenic variants are likely involved in a biologic pathway that is associated with glaucoma that occurs at lower intraocular pressures.
doi_str_mv 10.1001/jamaophthalmol.2024.3829
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E ; Tollefson, Mallory R ; Roos, Ben R ; Boese, Erin A ; Pouw, Andrew E ; Stone, Edwin M ; Schnieders, Michael J ; Fingert, John H</creator><creatorcontrib>Scheetz, Todd. E ; Tollefson, Mallory R ; Roos, Ben R ; Boese, Erin A ; Pouw, Andrew E ; Stone, Edwin M ; Schnieders, Michael J ; Fingert, John H</creatorcontrib><description>IMPORTANCE: This research confirms and further establishes that pathogenic variants in a fourth gene, METTL23, are associated with autosomal dominant normal-tension glaucoma (NTG). OBJECTIVE: To determine the frequency of glaucoma-causing pathogenic variants in the METTL23 gene in a cohort of patients with NTG from Iowa. DESIGN, SETTING, AND PARTICIPANTS: This case-control study took place at a single tertiary care center in Iowa from January 1997 to January 2024, with analysis occurring between January 2023 and January 2024. Two groups of participants were enrolled from the University of Iowa clinics: 331 patients with NTG and 362 control individuals without glaucoma. Patients with a history of trauma; steroid use; stigmata of pigment dispersion syndrome; exfoliation syndrome; or pathogenic variants in MYOC, TBK1, or OPTN were also excluded. MAIN OUTCOMES AND MEASURES: Detection of an enrichment of METTL23 pathogenic variants in individuals with NTG compared with control individuals without glaucoma. RESULTS: The study included 331 patients with NTG (mean [SD] age, 68.0 [11.7] years; 228 [68.9%] female and 103 [31.1%] male) and 362 control individuals without glaucoma (mean [SD] age, 64.5 [12.6] years; 207 [57.2%] female and 155 [42.8%] male). There were 5 detected instances of 4 unique METTL23 pathogenic variants in patients with NTG. Three METTL23 variants—p.Ala7Val, p.Pro22Arg, and p.Arg63Trp—were judged to be likely pathogenic and were detected in 3 patients (0.91%) with NTG. However, when all detected variants were evaluated with either mutation burden analysis or logistic regression, their frequency was not statistically higher in individuals with NTG than in control individuals without glaucoma (1.5% vs 2.5%; P = .27). CONCLUSION AND RELEVANCE: This investigation provides evidence that pathogenic variants in METTL23 are associated with NTG. Within an NTG cohort at a tertiary care center, pathogenic variants were associated with approximately 1% of NTG cases, a frequency similar to that of other known normal-tension glaucoma genes, including optineurin (OPTN), TANK-binding kinase 1 (TBK1), and myocilin (MYOC). 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E</creatorcontrib><creatorcontrib>Tollefson, Mallory R</creatorcontrib><creatorcontrib>Roos, Ben R</creatorcontrib><creatorcontrib>Boese, Erin A</creatorcontrib><creatorcontrib>Pouw, Andrew E</creatorcontrib><creatorcontrib>Stone, Edwin M</creatorcontrib><creatorcontrib>Schnieders, Michael J</creatorcontrib><creatorcontrib>Fingert, John H</creatorcontrib><title>METTL23 Variants and Patients With Normal-Tension Glaucoma</title><title>Archives of ophthalmology (1960)</title><addtitle>JAMA Ophthalmol</addtitle><description>IMPORTANCE: This research confirms and further establishes that pathogenic variants in a fourth gene, METTL23, are associated with autosomal dominant normal-tension glaucoma (NTG). OBJECTIVE: To determine the frequency of glaucoma-causing pathogenic variants in the METTL23 gene in a cohort of patients with NTG from Iowa. 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There were 5 detected instances of 4 unique METTL23 pathogenic variants in patients with NTG. Three METTL23 variants—p.Ala7Val, p.Pro22Arg, and p.Arg63Trp—were judged to be likely pathogenic and were detected in 3 patients (0.91%) with NTG. However, when all detected variants were evaluated with either mutation burden analysis or logistic regression, their frequency was not statistically higher in individuals with NTG than in control individuals without glaucoma (1.5% vs 2.5%; P = .27). CONCLUSION AND RELEVANCE: This investigation provides evidence that pathogenic variants in METTL23 are associated with NTG. Within an NTG cohort at a tertiary care center, pathogenic variants were associated with approximately 1% of NTG cases, a frequency similar to that of other known normal-tension glaucoma genes, including optineurin (OPTN), TANK-binding kinase 1 (TBK1), and myocilin (MYOC). 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E</au><au>Tollefson, Mallory R</au><au>Roos, Ben R</au><au>Boese, Erin A</au><au>Pouw, Andrew E</au><au>Stone, Edwin M</au><au>Schnieders, Michael J</au><au>Fingert, John H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>METTL23 Variants and Patients With Normal-Tension Glaucoma</atitle><jtitle>Archives of ophthalmology (1960)</jtitle><addtitle>JAMA Ophthalmol</addtitle><date>2024-11-01</date><risdate>2024</risdate><volume>142</volume><issue>11</issue><spage>1037</spage><epage>1045</epage><pages>1037-1045</pages><issn>2168-6165</issn><issn>2168-6173</issn><eissn>2168-6173</eissn><abstract>IMPORTANCE: This research confirms and further establishes that pathogenic variants in a fourth gene, METTL23, are associated with autosomal dominant normal-tension glaucoma (NTG). OBJECTIVE: To determine the frequency of glaucoma-causing pathogenic variants in the METTL23 gene in a cohort of patients with NTG from Iowa. DESIGN, SETTING, AND PARTICIPANTS: This case-control study took place at a single tertiary care center in Iowa from January 1997 to January 2024, with analysis occurring between January 2023 and January 2024. Two groups of participants were enrolled from the University of Iowa clinics: 331 patients with NTG and 362 control individuals without glaucoma. Patients with a history of trauma; steroid use; stigmata of pigment dispersion syndrome; exfoliation syndrome; or pathogenic variants in MYOC, TBK1, or OPTN were also excluded. MAIN OUTCOMES AND MEASURES: Detection of an enrichment of METTL23 pathogenic variants in individuals with NTG compared with control individuals without glaucoma. RESULTS: The study included 331 patients with NTG (mean [SD] age, 68.0 [11.7] years; 228 [68.9%] female and 103 [31.1%] male) and 362 control individuals without glaucoma (mean [SD] age, 64.5 [12.6] years; 207 [57.2%] female and 155 [42.8%] male). There were 5 detected instances of 4 unique METTL23 pathogenic variants in patients with NTG. Three METTL23 variants—p.Ala7Val, p.Pro22Arg, and p.Arg63Trp—were judged to be likely pathogenic and were detected in 3 patients (0.91%) with NTG. However, when all detected variants were evaluated with either mutation burden analysis or logistic regression, their frequency was not statistically higher in individuals with NTG than in control individuals without glaucoma (1.5% vs 2.5%; P = .27). CONCLUSION AND RELEVANCE: This investigation provides evidence that pathogenic variants in METTL23 are associated with NTG. Within an NTG cohort at a tertiary care center, pathogenic variants were associated with approximately 1% of NTG cases, a frequency similar to that of other known normal-tension glaucoma genes, including optineurin (OPTN), TANK-binding kinase 1 (TBK1), and myocilin (MYOC). The findings suggest that METTL23 pathogenic variants are likely involved in a biologic pathway that is associated with glaucoma that occurs at lower intraocular pressures.</abstract><cop>United States</cop><pub>American Medical Association</pub><pmid>39325437</pmid><doi>10.1001/jamaophthalmol.2024.3829</doi><tpages>9</tpages></addata></record>
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subjects Aged
Case-Control Studies
DNA Mutational Analysis
Female
Gene frequency
Glaucoma
Humans
Intraocular Pressure - physiology
Kinases
Low Tension Glaucoma - diagnosis
Low Tension Glaucoma - genetics
Low Tension Glaucoma - physiopathology
Male
Methyltransferases - genetics
Middle Aged
Mutation
Visual Fields - physiology
title METTL23 Variants and Patients With Normal-Tension Glaucoma
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