Differences in clinical presentation of primary open-angle glaucoma between African and European populations (2024)

Abstract

Purpose: Primary open-angle glaucoma (POAG) has been reported to occur more frequently in Africans, and to follow a more severe course compared to Europeans. We aimed to describe characteristics of POAG presentation and treatment across three ethnic groups from Africa and one from Europe. Methods: We ascertained 151 POAG patients from South African Coloured (SAC) and 94 South African Black (SAB) ethnicity from a university hospital in South Africa. In Tanzania, 310 patients were recruited from a university hospital and a referral hospital. In the Netherlands, 241 patients of European ancestry were included. All patients were over 35years old and had undergone an extensive ophthalmic examination. Patients were diagnosed according to the ISGEO criteria. A biogeographic ancestry analysis was performed to estimate the proportion of genetic African ancestry (GAA). Results: The biogeographic ancestry analysis showed that the median proportion of GAA was 97.6% in Tanzanian, 100% in SAB, 34.2% in SAC and 1.5% in Dutch participants. Clinical characteristics at presentation for Tanzanians, SAB, SAC and Dutch participants, respectively: mean age: 63, 57, 66, 70years (p<0.001); visual acuity in the worse eye: 1.78, 1.78, 0.3, 0.3 LogMAR (p<0.001); maximum intraocular pressure of both eyes: 36, 34, 29, 29mmHg (panova<0.001); maximum vertical cup to disc ratio (VCDR) of both eyes: 0.90, 0.90, 0.84, 0.83 (p<0.001); mean central corneal thickness: 506, 487, 511, 528μm (p<0.001). Fourteen percent of Tanzanian patients presented with blindness (<3/60 Snellen) in the better eye in contrast to only 1% in the Dutch. Conclusion: In this multi-ethnic comparative study, Sub-Saharan Africans present at a younger age with lower visual acuity, higher IOP, larger VCDR, than SAC and Dutch participants. This indicates the more progressive and destructive course in Sub-Saharan Africans.

Original languageEnglish
Pages (from-to)e1118-e1126
JournalActa Ophthalmologica
Volume99
Issue number7
Early online date8 Feb 2021
DOIs
Publication statusPublished - Nov 2021

Bibliographical note

Funding Information:
Stichting Combined Ophthalmic Research Rotterdam (CORR), BrightFocus Foundation, Algemene Nederlandse Vereniging ter Voorkoming van blindheid, Landelijke Stichting voor Blinden en Slechtzienden, Stichting Beheer het Schild, Prof. dr. Henkes stichting, Rotterdamse Stichting Blindenbelangen, Stichting Glaucoomfonds. European Union Horizon 2020 research and innovation programme under the Marie Sk?odowska-Curie grant agreement No. 675033 (EGRET plus). The GLGS is supported by the Dutch Health Care Insurance Council (CVZ) through the Department of Medical Technology Assessment (MTA) of the University Hospital Groningen, the Netherlands. N.M. Jansonius received the funding for this study from the European Union Horizon 2020 research and innovation programme under the Marie Sk?odowska-Curie grant agreement No. 675033 (EGRET plus). The authors thank all the GIGA study participants for their cooperation. We gratefully acknowledge Suzanne van Schaik, Milou van Bruchem, Hannah Hardjosantoso, Katinka Snoek, Chawan Amin, Vicky Hokken, Corina Brussee, Hilda Roothaert and all ophthalmologist, residents and nurses of the Ophthalmology departments from the Groote Schuur Hospital, Muhimbili National Hospital and CCBRT for their continuous efforts in the recruitment of participants. The GIGA study is supported by grants from Combined Ophthalmic Research Rotterdam, The Netherlands; BrightFocus Foundation (G2015084), USA; UitZicht grant No 2014-22 and 2015-32 (Algemene Nederlandse Vereniging ter Voorkoming van Blindheid, The Netherlands; Landelijke Stichting voor Blinden en Slechtzienden, The Netherlands; Stichting Beheer Het Schild, The Netherlands; Stichting Glaucoomfonds, The Netherlands); Prof. Dr. Henkes stichting, The Netherlands; Rotterdamse Stichting Blindenbelangen, The Netherlands.

Funding Information:
Stichting Combined Ophthalmic Research Rotterdam (CORR), BrightFocus Foundation, Algemene Nederlandse Vereniging ter Voorkoming van blindheid, Landelijke Stichting voor Blinden en Slechtzienden, Stichting Beheer het Schild, Prof. dr. Henkes stichting, Rotterdamse Stichting Blindenbelangen, Stichting Glaucoomfonds. European Union Horizon 2020 research and innovation programme under the Marie Skłodowska‐Curie grant agreement No. 675033 (EGRET plus).

Funding Information:
The GLGS is supported by the Dutch Health Care Insurance Council (CVZ) through the Department of Medical Technology Assessment (MTA) of the University Hospital Groningen, the Netherlands. N.M. Jansonius received the funding for this study from the European Union Horizon 2020 research and innovation programme under the Marie Skłodowska‐Curie grant agreement No. 675033 (EGRET plus).

Funding Information:
The authors thank all the GIGA study participants for their cooperation. We gratefully acknowledge Suzanne van Schaik, Milou van Bruchem, Hannah Hardjosantoso, Katinka Snoek, Chawan Amin, Vicky Hokken, Corina Brussee, Hilda Roothaert and all ophthalmologist, residents and nurses of the Ophthalmology departments from the Groote Schuur Hospital, Muhimbili National Hospital and CCBRT for their continuous efforts in the recruitment of participants. The GIGA study is supported by grants from Combined Ophthalmic Research Rotterdam, The Netherlands; BrightFocus Foundation (G2015084), USA; UitZicht grant No 2014‐22 and 2015‐32 (Algemene Nederlandse Vereniging ter Voorkoming van Blindheid, The Netherlands; Landelijke Stichting voor Blinden en Slechtzienden, The Netherlands; Stichting Beheer Het Schild, The Netherlands; Stichting Glaucoomfonds, The Netherlands); Prof. Dr. Henkes stichting, The Netherlands; Rotterdamse Stichting Blindenbelangen, The Netherlands.

Publisher Copyright:
© 2021 The Authors. Acta Ophthalmologica published by John Wiley & Sons Ltd on behalf of Acta Ophthalmologica Scandinavica Foundation.

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    Bonnemaijer, P. W. M., Lo Faro, V., GIGA study group, Sanyiwa, A. J., Hassan, H. G., Cook, C., Van de Laar, S., Lemij, H. G., Klaver, C. C. W., Jansonius, N. M. (2021). Differences in clinical presentation of primary open-angle glaucoma between African and European populations. Acta Ophthalmologica, 99(7), e1118-e1126. https://doi.org/10.1111/aos.14772

    Bonnemaijer, Pieter W.M. ; Lo Faro, Valeria ; GIGA study group et al. / Differences in clinical presentation of primary open-angle glaucoma between African and European populations. In: Acta Ophthalmologica. 2021 ; Vol. 99, No. 7. pp. e1118-e1126.

    @article{37892abf17ba4fc0a2f86025c9814ad0,

    title = "Differences in clinical presentation of primary open-angle glaucoma between African and European populations",

    abstract = "Purpose: Primary open-angle glaucoma (POAG) has been reported to occur more frequently in Africans, and to follow a more severe course compared to Europeans. We aimed to describe characteristics of POAG presentation and treatment across three ethnic groups from Africa and one from Europe. Methods: We ascertained 151 POAG patients from South African Coloured (SAC) and 94 South African Black (SAB) ethnicity from a university hospital in South Africa. In Tanzania, 310 patients were recruited from a university hospital and a referral hospital. In the Netherlands, 241 patients of European ancestry were included. All patients were over 35years old and had undergone an extensive ophthalmic examination. Patients were diagnosed according to the ISGEO criteria. A biogeographic ancestry analysis was performed to estimate the proportion of genetic African ancestry (GAA). Results: The biogeographic ancestry analysis showed that the median proportion of GAA was 97.6% in Tanzanian, 100% in SAB, 34.2% in SAC and 1.5% in Dutch participants. Clinical characteristics at presentation for Tanzanians, SAB, SAC and Dutch participants, respectively: mean age: 63, 57, 66, 70years (p<0.001); visual acuity in the worse eye: 1.78, 1.78, 0.3, 0.3 LogMAR (p<0.001); maximum intraocular pressure of both eyes: 36, 34, 29, 29mmHg (panova<0.001); maximum vertical cup to disc ratio (VCDR) of both eyes: 0.90, 0.90, 0.84, 0.83 (p<0.001); mean central corneal thickness: 506, 487, 511, 528μm (p<0.001). Fourteen percent of Tanzanian patients presented with blindness (<3/60 Snellen) in the better eye in contrast to only 1% in the Dutch. Conclusion: In this multi-ethnic comparative study, Sub-Saharan Africans present at a younger age with lower visual acuity, higher IOP, larger VCDR, than SAC and Dutch participants. This indicates the more progressive and destructive course in Sub-Saharan Africans.",

    author = "Bonnemaijer, {Pieter W.M.} and {Lo Faro}, Valeria and {GIGA study group} and Sanyiwa, {Anna J.} and Hassan, {Hassan G.} and Colin Cook and {Van de Laar}, Suzanne and Lemij, {Hans G.} and Klaver, {Caroline C.W.} and Jansonius, {Nomdo M.} and Thiadens, {Alberta A.H.J.} and Neema Kanyaro and Cyprian Ntomoka and Massaga, {Julius J.} and Ikungura, {Joyce K.} and Angelina Ampong and Doreen Nelson-Ayifah and Sjoerd Driessen",

    note = "Funding Information: Stichting Combined Ophthalmic Research Rotterdam (CORR), BrightFocus Foundation, Algemene Nederlandse Vereniging ter Voorkoming van blindheid, Landelijke Stichting voor Blinden en Slechtzienden, Stichting Beheer het Schild, Prof. dr. Henkes stichting, Rotterdamse Stichting Blindenbelangen, Stichting Glaucoomfonds. European Union Horizon 2020 research and innovation programme under the Marie Sk?odowska-Curie grant agreement No. 675033 (EGRET plus). The GLGS is supported by the Dutch Health Care Insurance Council (CVZ) through the Department of Medical Technology Assessment (MTA) of the University Hospital Groningen, the Netherlands. N.M. Jansonius received the funding for this study from the European Union Horizon 2020 research and innovation programme under the Marie Sk?odowska-Curie grant agreement No. 675033 (EGRET plus). The authors thank all the GIGA study participants for their cooperation. We gratefully acknowledge Suzanne van Schaik, Milou van Bruchem, Hannah Hardjosantoso, Katinka Snoek, Chawan Amin, Vicky Hokken, Corina Brussee, Hilda Roothaert and all ophthalmologist, residents and nurses of the Ophthalmology departments from the Groote Schuur Hospital, Muhimbili National Hospital and CCBRT for their continuous efforts in the recruitment of participants. The GIGA study is supported by grants from Combined Ophthalmic Research Rotterdam, The Netherlands; BrightFocus Foundation (G2015084), USA; UitZicht grant No 2014-22 and 2015-32 (Algemene Nederlandse Vereniging ter Voorkoming van Blindheid, The Netherlands; Landelijke Stichting voor Blinden en Slechtzienden, The Netherlands; Stichting Beheer Het Schild, The Netherlands; Stichting Glaucoomfonds, The Netherlands); Prof. Dr. Henkes stichting, The Netherlands; Rotterdamse Stichting Blindenbelangen, The Netherlands. Funding Information: Stichting Combined Ophthalmic Research Rotterdam (CORR), BrightFocus Foundation, Algemene Nederlandse Vereniging ter Voorkoming van blindheid, Landelijke Stichting voor Blinden en Slechtzienden, Stichting Beheer het Schild, Prof. dr. Henkes stichting, Rotterdamse Stichting Blindenbelangen, Stichting Glaucoomfonds. European Union Horizon 2020 research and innovation programme under the Marie Sk{\l}odowska‐Curie grant agreement No. 675033 (EGRET plus). Funding Information: The GLGS is supported by the Dutch Health Care Insurance Council (CVZ) through the Department of Medical Technology Assessment (MTA) of the University Hospital Groningen, the Netherlands. N.M. Jansonius received the funding for this study from the European Union Horizon 2020 research and innovation programme under the Marie Sk{\l}odowska‐Curie grant agreement No. 675033 (EGRET plus). Funding Information: The authors thank all the GIGA study participants for their cooperation. We gratefully acknowledge Suzanne van Schaik, Milou van Bruchem, Hannah Hardjosantoso, Katinka Snoek, Chawan Amin, Vicky Hokken, Corina Brussee, Hilda Roothaert and all ophthalmologist, residents and nurses of the Ophthalmology departments from the Groote Schuur Hospital, Muhimbili National Hospital and CCBRT for their continuous efforts in the recruitment of participants. The GIGA study is supported by grants from Combined Ophthalmic Research Rotterdam, The Netherlands; BrightFocus Foundation (G2015084), USA; UitZicht grant No 2014‐22 and 2015‐32 (Algemene Nederlandse Vereniging ter Voorkoming van Blindheid, The Netherlands; Landelijke Stichting voor Blinden en Slechtzienden, The Netherlands; Stichting Beheer Het Schild, The Netherlands; Stichting Glaucoomfonds, The Netherlands); Prof. Dr. Henkes stichting, The Netherlands; Rotterdamse Stichting Blindenbelangen, The Netherlands. Publisher Copyright: {\textcopyright} 2021 The Authors. Acta Ophthalmologica published by John Wiley & Sons Ltd on behalf of Acta Ophthalmologica Scandinavica Foundation.",

    year = "2021",

    month = nov,

    doi = "10.1111/aos.14772",

    language = "English",

    volume = "99",

    pages = "e1118--e1126",

    journal = "Acta Ophthalmologica",

    issn = "1755-375X",

    publisher = "Wiley-Blackwell Publishing Ltd",

    number = "7",

    }

    Bonnemaijer, PWM, Lo Faro, V, GIGA study group, Sanyiwa, AJ, Hassan, HG, Cook, C, Van de Laar, S, Lemij, HG, Klaver, CCW, Jansonius, NM 2021, 'Differences in clinical presentation of primary open-angle glaucoma between African and European populations', Acta Ophthalmologica, vol. 99, no. 7, pp. e1118-e1126. https://doi.org/10.1111/aos.14772

    Differences in clinical presentation of primary open-angle glaucoma between African and European populations. / Bonnemaijer, Pieter W.M.; Lo Faro, Valeria; GIGA study group et al.
    In: Acta Ophthalmologica, Vol. 99, No. 7, 11.2021, p. e1118-e1126.

    Research output: Contribution to journalArticleAcademicpeer-review

    TY - JOUR

    T1 - Differences in clinical presentation of primary open-angle glaucoma between African and European populations

    AU - Bonnemaijer, Pieter W.M.

    AU - Lo Faro, Valeria

    AU - GIGA study group

    AU - Sanyiwa, Anna J.

    AU - Hassan, Hassan G.

    AU - Cook, Colin

    AU - Van de Laar, Suzanne

    AU - Lemij, Hans G.

    AU - Klaver, Caroline C.W.

    AU - Jansonius, Nomdo M.

    AU - Thiadens, Alberta A.H.J.

    AU - Kanyaro, Neema

    AU - Ntomoka, Cyprian

    AU - Massaga, Julius J.

    AU - Ikungura, Joyce K.

    AU - Ampong, Angelina

    AU - Nelson-Ayifah, Doreen

    AU - Driessen, Sjoerd

    N1 - Funding Information:Stichting Combined Ophthalmic Research Rotterdam (CORR), BrightFocus Foundation, Algemene Nederlandse Vereniging ter Voorkoming van blindheid, Landelijke Stichting voor Blinden en Slechtzienden, Stichting Beheer het Schild, Prof. dr. Henkes stichting, Rotterdamse Stichting Blindenbelangen, Stichting Glaucoomfonds. European Union Horizon 2020 research and innovation programme under the Marie Sk?odowska-Curie grant agreement No. 675033 (EGRET plus). The GLGS is supported by the Dutch Health Care Insurance Council (CVZ) through the Department of Medical Technology Assessment (MTA) of the University Hospital Groningen, the Netherlands. N.M. Jansonius received the funding for this study from the European Union Horizon 2020 research and innovation programme under the Marie Sk?odowska-Curie grant agreement No. 675033 (EGRET plus). The authors thank all the GIGA study participants for their cooperation. We gratefully acknowledge Suzanne van Schaik, Milou van Bruchem, Hannah Hardjosantoso, Katinka Snoek, Chawan Amin, Vicky Hokken, Corina Brussee, Hilda Roothaert and all ophthalmologist, residents and nurses of the Ophthalmology departments from the Groote Schuur Hospital, Muhimbili National Hospital and CCBRT for their continuous efforts in the recruitment of participants. The GIGA study is supported by grants from Combined Ophthalmic Research Rotterdam, The Netherlands; BrightFocus Foundation (G2015084), USA; UitZicht grant No 2014-22 and 2015-32 (Algemene Nederlandse Vereniging ter Voorkoming van Blindheid, The Netherlands; Landelijke Stichting voor Blinden en Slechtzienden, The Netherlands; Stichting Beheer Het Schild, The Netherlands; Stichting Glaucoomfonds, The Netherlands); Prof. Dr. Henkes stichting, The Netherlands; Rotterdamse Stichting Blindenbelangen, The Netherlands.Funding Information:Stichting Combined Ophthalmic Research Rotterdam (CORR), BrightFocus Foundation, Algemene Nederlandse Vereniging ter Voorkoming van blindheid, Landelijke Stichting voor Blinden en Slechtzienden, Stichting Beheer het Schild, Prof. dr. Henkes stichting, Rotterdamse Stichting Blindenbelangen, Stichting Glaucoomfonds. European Union Horizon 2020 research and innovation programme under the Marie Skłodowska‐Curie grant agreement No. 675033 (EGRET plus). Funding Information:The GLGS is supported by the Dutch Health Care Insurance Council (CVZ) through the Department of Medical Technology Assessment (MTA) of the University Hospital Groningen, the Netherlands. N.M. Jansonius received the funding for this study from the European Union Horizon 2020 research and innovation programme under the Marie Skłodowska‐Curie grant agreement No. 675033 (EGRET plus). Funding Information:The authors thank all the GIGA study participants for their cooperation. We gratefully acknowledge Suzanne van Schaik, Milou van Bruchem, Hannah Hardjosantoso, Katinka Snoek, Chawan Amin, Vicky Hokken, Corina Brussee, Hilda Roothaert and all ophthalmologist, residents and nurses of the Ophthalmology departments from the Groote Schuur Hospital, Muhimbili National Hospital and CCBRT for their continuous efforts in the recruitment of participants. The GIGA study is supported by grants from Combined Ophthalmic Research Rotterdam, The Netherlands; BrightFocus Foundation (G2015084), USA; UitZicht grant No 2014‐22 and 2015‐32 (Algemene Nederlandse Vereniging ter Voorkoming van Blindheid, The Netherlands; Landelijke Stichting voor Blinden en Slechtzienden, The Netherlands; Stichting Beheer Het Schild, The Netherlands; Stichting Glaucoomfonds, The Netherlands); Prof. Dr. Henkes stichting, The Netherlands; Rotterdamse Stichting Blindenbelangen, The Netherlands. Publisher Copyright:© 2021 The Authors. Acta Ophthalmologica published by John Wiley & Sons Ltd on behalf of Acta Ophthalmologica Scandinavica Foundation.

    PY - 2021/11

    Y1 - 2021/11

    N2 - Purpose: Primary open-angle glaucoma (POAG) has been reported to occur more frequently in Africans, and to follow a more severe course compared to Europeans. We aimed to describe characteristics of POAG presentation and treatment across three ethnic groups from Africa and one from Europe. Methods: We ascertained 151 POAG patients from South African Coloured (SAC) and 94 South African Black (SAB) ethnicity from a university hospital in South Africa. In Tanzania, 310 patients were recruited from a university hospital and a referral hospital. In the Netherlands, 241 patients of European ancestry were included. All patients were over 35years old and had undergone an extensive ophthalmic examination. Patients were diagnosed according to the ISGEO criteria. A biogeographic ancestry analysis was performed to estimate the proportion of genetic African ancestry (GAA). Results: The biogeographic ancestry analysis showed that the median proportion of GAA was 97.6% in Tanzanian, 100% in SAB, 34.2% in SAC and 1.5% in Dutch participants. Clinical characteristics at presentation for Tanzanians, SAB, SAC and Dutch participants, respectively: mean age: 63, 57, 66, 70years (p<0.001); visual acuity in the worse eye: 1.78, 1.78, 0.3, 0.3 LogMAR (p<0.001); maximum intraocular pressure of both eyes: 36, 34, 29, 29mmHg (panova<0.001); maximum vertical cup to disc ratio (VCDR) of both eyes: 0.90, 0.90, 0.84, 0.83 (p<0.001); mean central corneal thickness: 506, 487, 511, 528μm (p<0.001). Fourteen percent of Tanzanian patients presented with blindness (<3/60 Snellen) in the better eye in contrast to only 1% in the Dutch. Conclusion: In this multi-ethnic comparative study, Sub-Saharan Africans present at a younger age with lower visual acuity, higher IOP, larger VCDR, than SAC and Dutch participants. This indicates the more progressive and destructive course in Sub-Saharan Africans.

    AB - Purpose: Primary open-angle glaucoma (POAG) has been reported to occur more frequently in Africans, and to follow a more severe course compared to Europeans. We aimed to describe characteristics of POAG presentation and treatment across three ethnic groups from Africa and one from Europe. Methods: We ascertained 151 POAG patients from South African Coloured (SAC) and 94 South African Black (SAB) ethnicity from a university hospital in South Africa. In Tanzania, 310 patients were recruited from a university hospital and a referral hospital. In the Netherlands, 241 patients of European ancestry were included. All patients were over 35years old and had undergone an extensive ophthalmic examination. Patients were diagnosed according to the ISGEO criteria. A biogeographic ancestry analysis was performed to estimate the proportion of genetic African ancestry (GAA). Results: The biogeographic ancestry analysis showed that the median proportion of GAA was 97.6% in Tanzanian, 100% in SAB, 34.2% in SAC and 1.5% in Dutch participants. Clinical characteristics at presentation for Tanzanians, SAB, SAC and Dutch participants, respectively: mean age: 63, 57, 66, 70years (p<0.001); visual acuity in the worse eye: 1.78, 1.78, 0.3, 0.3 LogMAR (p<0.001); maximum intraocular pressure of both eyes: 36, 34, 29, 29mmHg (panova<0.001); maximum vertical cup to disc ratio (VCDR) of both eyes: 0.90, 0.90, 0.84, 0.83 (p<0.001); mean central corneal thickness: 506, 487, 511, 528μm (p<0.001). Fourteen percent of Tanzanian patients presented with blindness (<3/60 Snellen) in the better eye in contrast to only 1% in the Dutch. Conclusion: In this multi-ethnic comparative study, Sub-Saharan Africans present at a younger age with lower visual acuity, higher IOP, larger VCDR, than SAC and Dutch participants. This indicates the more progressive and destructive course in Sub-Saharan Africans.

    UR - http://www.scopus.com/inward/record.url?scp=85100562282&partnerID=8YFLogxK

    U2 - 10.1111/aos.14772

    DO - 10.1111/aos.14772

    M3 - Article

    C2 - 33555657

    AN - SCOPUS:85100562282

    SN - 1755-375X

    VL - 99

    SP - e1118-e1126

    JO - Acta Ophthalmologica

    JF - Acta Ophthalmologica

    IS - 7

    ER -

    Bonnemaijer PWM, Lo Faro V, GIGA study group, Sanyiwa AJ, Hassan HG, Cook C et al. Differences in clinical presentation of primary open-angle glaucoma between African and European populations. Acta Ophthalmologica. 2021 Nov;99(7):e1118-e1126. Epub 2021 Feb 8. doi: 10.1111/aos.14772

    Differences in clinical presentation of primary open-angle glaucoma between African and European populations (2024)

    FAQs

    Do African Americans get primary open-angle glaucoma? ›

    According to the National Institutes of Health, African Americans are five times more likely to develop glaucoma and six times more likely to go blind from glaucoma. Unfortunately, in African Americans, glaucoma can also occur earlier in life — on average, about 10 years earlier than in other ethnic populations.

    What is the difference between open-angle glaucoma and primary open-angle glaucoma? ›

    Primary Open-Angle Glaucoma, the most common form of glaucoma and also called Open-Angle Glaucoma, is a lifelong condition that accounts for at least 90% of all glaucoma cases. In Open-Angle Glaucoma, the eye's drainage canals become clogged over time. This can damage the optic nerve.

    Does glaucoma affect specific populations of people more so than other populations? ›

    Anyone can get glaucoma, but African Americans over age 40, all people over age 60 and those with a family history of glaucoma or diabetes are at higher risk. After cataracts, glaucoma is the leading cause of blindness among African Americans, who are six to eight times more likely to get the disease than white people.

    What is the prevalence of primary open-angle glaucoma in Africa? ›

    The global prevalence of glaucoma was estimated at 2.4% in 2021 [4]. In Africa (2021), glaucoma prevalence was estimated at 4.2% for primary open-angle glaucoma (POAG) and 1.09% for primary angle-closure glaucoma (PACG) [3, 4].

    Who has higher prevalence of primary open-angle glaucoma? ›

    POAG is strongly correlated with age: its prevalence is highest among older Hispanic or Latino individuals (18%), black individuals (15%), white individuals (7%), and Asian individuals (5%) [6]. Finally, there are gender differences in glaucoma as well.

    What is the race ethnicity and prevalence of primary open-angle glaucoma? ›

    The disease burden for primary open-angle glaucoma (POAG) is highest among racial/ethnic minority groups, particularly Black individuals. The prevalence of POAG worldwide is projected to increase from 52.7 million in 2020 to 79.8 million in 2040, a 51.4% increase attributed mainly to Asian and African individuals.

    What is a differential diagnosis of primary open angle glaucoma? ›

    Differential diagnoses to consider include: Ocular hypertension (elevated IOP but no definite signs of glaucomatous optic neuropathy) Normal tension glaucoma (all the features of POAG but IOP always measured within normal limits) Primary angle closure glaucoma (narrow drainage angle on gonioscopy)

    What is the difference between POAG and PACG? ›

    There are two types of primary glaucoma: primary open-angle glaucoma (POAG) and primary angle-closure glaucoma (PACG). POAG is characterized by an open iridocorneal angle, and in contrast, PACG is characterized by a narrow or closed iridocorneal angle that hampers the aqueous efflux, which can lead to increased IOP.

    What is the difference between the two types of glaucoma? ›

    In open-angle glaucoma, the increase in pressure is often small and slow. In closed-angle glaucoma, the increase is often high and sudden. Either type can damage the optic nerve.

    What ethnicity has open-angle glaucoma? ›

    In the United States, the leading cause of irreversible blindness among Americans of African descent is primary open-angle glaucoma (POAG). POAG affects this population at a younger age than other groups (about a decade earlier) and it is often diagnosed at a more severe stage of disease.

    What is the racial disparity in glaucoma? ›

    In the US, an estimated 3 million adults have glaucoma, with African Americans having a higher prevalence of the disease than other racial and ethnic groups.

    Which ethnicity is at the highest risk for glaucoma? ›

    Although everyone is at risk for glaucoma, those at higher risk include people who: Are over 60 years old. Are of African, Asian, or Hispanic descent.

    What are the racial variations in the prevalence of primary open-angle glaucoma the Baltimore eye survey? ›

    Main Results. —Age-adjusted prevalence rates for primary open-angle glaucoma were four to five times higher in blacks as compared with whites. Rates among blacks ranged from 1.23% in those aged 40 through 49 years to 11.26% in those 80 years or older, whereas rates for whites ranged from 0.92% to 2.16%, respectively.

    What is the demographic of open angle glaucoma? ›

    The largest number of persons with POAG is among those aged 70–79 (31%), followed by those aged 60–69 (27%), aged 50–59 (17%), aged 80 and older (17%), and aged 40–49 (8%).

    What is the prevalence and types of glaucoma among an indigenous African population in southwestern Nigeria? ›

    Conclusions.: The high prevalence of glaucoma (7.3%) in the Akinyele district in southwestern Nigeria is comparable with those in predominantly black populations in the Akwapim-South district of Ghana and Barbados. Primary open angle glaucoma remains the most prevalent form of glaucoma.

    Who is at risk of primary open-angle glaucoma? ›

    Some of the risk factors for primary open-angle glaucoma have been extensively described and studied, including elevated intraocular pressure, advancing age, family history, African ancestry, myopia, and perhaps presence of certain systemic diseases, such as diabetes and hypertension.

    Which patient is most likely to have open-angle glaucoma? ›

    Open-angle glaucoma tends to run in families. Your risk is higher if you have a parent or grandparent with open-angle glaucoma. People of African descent are also at higher risk for this disease.

    What is the demographic of open-angle glaucoma? ›

    The largest number of persons with POAG is among those aged 70–79 (31%), followed by those aged 60–69 (27%), aged 50–59 (17%), aged 80 and older (17%), and aged 40–49 (8%).

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