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 |
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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). 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.</description><identifier>ISSN: 2168-6165</identifier><identifier>ISSN: 2168-6173</identifier><identifier>EISSN: 2168-6173</identifier><identifier>DOI: 10.1001/jamaophthalmol.2024.3829</identifier><identifier>PMID: 39325437</identifier><language>eng</language><publisher>United States: American Medical Association</publisher><subject>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</subject><ispartof>Archives of ophthalmology (1960), 2024-11, Vol.142 (11), p.1037-1045</ispartof><rights>Copyright American Medical Association Nov 2024</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a237t-35045da9a9a9e707e6fc365ede99fbbec452e6b21e8914713f0866c807a42ce13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://jamanetwork.com/journals/jamaophthalmology/articlepdf/10.1001/jamaophthalmol.2024.3829$$EPDF$$P50$$Gama$$H</linktopdf><linktohtml>$$Uhttps://jamanetwork.com/journals/jamaophthalmology/fullarticle/10.1001/jamaophthalmol.2024.3829$$EHTML$$P50$$Gama$$H</linktohtml><link.rule.ids>64,314,776,780,3327,27901,27902,76458,76461</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39325437$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Scheetz, Todd. 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. 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.</description><subject>Aged</subject><subject>Case-Control Studies</subject><subject>DNA Mutational Analysis</subject><subject>Female</subject><subject>Gene frequency</subject><subject>Glaucoma</subject><subject>Humans</subject><subject>Intraocular Pressure - physiology</subject><subject>Kinases</subject><subject>Low Tension Glaucoma - diagnosis</subject><subject>Low Tension Glaucoma - genetics</subject><subject>Low Tension Glaucoma - physiopathology</subject><subject>Male</subject><subject>Methyltransferases - genetics</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Visual Fields - physiology</subject><issn>2168-6165</issn><issn>2168-6173</issn><issn>2168-6173</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkDtPwzAQgC0EolXpH2BAkVhYUvyKH2yoKgWpPIYAo3VJHTVVEhc7Gfj3JGqpBHfD-eTvztaHUETwjGBMbrdQg9tt2g1UtatmFFM-Y4rqEzSmRKhYEMlOj2eRjNA0hC3uQ2HMWXKORkwzmnAmx-jueZGmK8qiD_AlNG2IoFlHb9CWdmg-y3YTvThfQxWntgmla6JlBV3uarhAZwVUwU4PdYLeHxbp_DFevS6f5verGCiTbcwSzJM16CGtxNKKImcisWurdZFlNucJtSKjxCpNuCSswEqIXGEJnOaWsAm62e_deffV2dCaugy5rSporOuCYQRrLYUUA3r9D926zjf973qKayoU07Kn1J7KvQvB28LsfFmD_zYEm0Gx-avYDIrNoLgfvTo80GW1XR8Hf4X2wOUe6Dccb6miHGvCfgCjI4G9</recordid><startdate>20241101</startdate><enddate>20241101</enddate><creator>Scheetz, Todd. 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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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of ophthalmology (1960)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Scheetz, Todd. 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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