Prevalence of Alpha-1 Antitrypsin Deficiency, Self-Reported Behavior Change, and Health Care Engagement Among Direct-to-Consumer Recipients of a Personalized Genetic Risk Report
Alpha-1 antitrypsin deficiency (AATD) is an autosomal co-dominant condition that predisposes to emphysema, cirrhosis, panniculitis, and vasculitis. Underrecognition has prompted efforts to enhance early detection and testing of at-risk individuals. Direct-to-consumer (DTC) genetic testing represents...
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Veröffentlicht in: | Chest 2022-02, Vol.161 (2), p.373-381 |
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creator | Ashenhurst, James R. Nhan, Hoang Shelton, Janie F. Wu, Shirley Tung, Joyce Y. Elson, Sarah L. Stoller, James K. Agee, Michelle Aslibekyan, Stella Auton, Adam Babalola, Elizabeth Bell, Robert K. Bielenberg, Jessica Bryc, Katarzyna Bullis, Emily Cameron, Briana Coker, Daniella Partida, Gabriel Cuellar Dhamija, Devika Das, Sayantan Elson, Sarah L. Filshtein, Teresa Fletez-Brant, Kipper Fontanillas, Pierre Freyman, Will Gandhi, Pooja M. Heilbron, Karl Hicks, Barry Hinds, David A. Huber, Karen E. Jewett, Ethan M. Jiang, Yunxuan Kleinman, Aaron Kukar, Katelyn Lane, Vanessa A. Lin, Keng-Han Lowe, Maya Luff, Marie K. McCreight, Jennifer C. McIntyre, Matthew H. McManus, Kimberly F. Micheletti, Steven J. Moreno, Meghan E. Mountain, Joanna L. Mozaffari, Sahar V. Nandakumar, Priyanka Noblin, Elizabeth S. O’Connell, Jared Petrakovitz, Aaron A. Poznik, G. David Schumacher, Morgan Shastri, Anjali J. Shelton, Janie F. Shi, Jingchunzi Shringarpure, Suyash Tian, Chao Tran, Vinh Tung, Joyce Y. Wang, Xin Wang, Wei Weldon, Catherine H. Wilton, Peter |
description | Alpha-1 antitrypsin deficiency (AATD) is an autosomal co-dominant condition that predisposes to emphysema, cirrhosis, panniculitis, and vasculitis. Underrecognition has prompted efforts to enhance early detection and testing of at-risk individuals. Direct-to-consumer (DTC) genetic testing represents an additional method of detection.
The study addressed three questions: (1) Does a DTC testing service identify previously undetected individuals with AATD? (2) What was the interval between initial AATD-related symptoms and initial diagnosis of AATD in such individuals? and (3) What was the behavioral impact of learning about a new diagnosis of AATD through a DTC test?
In this cross-sectional study, 195,014 individuals responded to a survey within the 23andMe, Inc. research platform.
Among 195,014 study participants, the allele frequency for the PI∗S and PI∗Z AATD variants was 21.6% (6.5% for PI∗Z and 15.1% for PI∗S); 0.63% were PI∗ZZ, half of whom reported having a physician confirm the diagnosis. Approximately 27% of those with physician-diagnosed AATD reported first becoming aware of AATD through the DTC test. Among those newly aware participants, the diagnostic delay interval was 22.3 years. Participants frequently shared their DTC test results with health care providers (HCPs) and the reported impact of learning a diagnosis of AATD was high. For example, 51.1% of PI∗ZZ individuals shared their DTC result with an HCP. The OR for PI∗ZZ smokers to report smoking reduction as a result of receiving the DTC result was 1.7 (95% CI = 1.4-2.2) compared with those without a Z allele and for reduced alcohol consumption this was 4.0 (95% CI = 2.6-5.9).
In this largest available report on DTC testing for AATD, this test, in combination with clinical follow-up, can help to identify previously undiagnosed AATD patients. Moreover, receipt of the DTC AATD report was associated with positive behavior change, especially among those with risk variants.
[Display omitted] |
doi_str_mv | 10.1016/j.chest.2021.09.041 |
format | Article |
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The study addressed three questions: (1) Does a DTC testing service identify previously undetected individuals with AATD? (2) What was the interval between initial AATD-related symptoms and initial diagnosis of AATD in such individuals? and (3) What was the behavioral impact of learning about a new diagnosis of AATD through a DTC test?
In this cross-sectional study, 195,014 individuals responded to a survey within the 23andMe, Inc. research platform.
Among 195,014 study participants, the allele frequency for the PI∗S and PI∗Z AATD variants was 21.6% (6.5% for PI∗Z and 15.1% for PI∗S); 0.63% were PI∗ZZ, half of whom reported having a physician confirm the diagnosis. Approximately 27% of those with physician-diagnosed AATD reported first becoming aware of AATD through the DTC test. Among those newly aware participants, the diagnostic delay interval was 22.3 years. Participants frequently shared their DTC test results with health care providers (HCPs) and the reported impact of learning a diagnosis of AATD was high. For example, 51.1% of PI∗ZZ individuals shared their DTC result with an HCP. The OR for PI∗ZZ smokers to report smoking reduction as a result of receiving the DTC result was 1.7 (95% CI = 1.4-2.2) compared with those without a Z allele and for reduced alcohol consumption this was 4.0 (95% CI = 2.6-5.9).
In this largest available report on DTC testing for AATD, this test, in combination with clinical follow-up, can help to identify previously undiagnosed AATD patients. Moreover, receipt of the DTC AATD report was associated with positive behavior change, especially among those with risk variants.
[Display omitted]</description><identifier>ISSN: 0012-3692</identifier><identifier>EISSN: 1931-3543</identifier><identifier>DOI: 10.1016/j.chest.2021.09.041</identifier><identifier>PMID: 34656525</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>AATD ; alpha 1-Antitrypsin Deficiency - epidemiology ; alpha 1-Antitrypsin Deficiency - genetics ; alpha-1 antitrypsin deficiency ; consumer genomics ; direct-to-consumer ; Direct-To-Consumer Screening and Testing ; Female ; Genetic Testing ; Genotype ; Humans ; lung disease ; Male ; Middle Aged ; Prevalence ; rare disease ; Self Report ; SERPINA1</subject><ispartof>Chest, 2022-02, Vol.161 (2), p.373-381</ispartof><rights>2021 The Author(s)</rights><rights>Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-641740c0b7d081ff9bac3bf789d897360e893ddb2dddb8ede80a241079421a593</citedby><cites>FETCH-LOGICAL-c404t-641740c0b7d081ff9bac3bf789d897360e893ddb2dddb8ede80a241079421a593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34656525$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ashenhurst, James R.</creatorcontrib><creatorcontrib>Nhan, Hoang</creatorcontrib><creatorcontrib>Shelton, Janie F.</creatorcontrib><creatorcontrib>Wu, Shirley</creatorcontrib><creatorcontrib>Tung, Joyce Y.</creatorcontrib><creatorcontrib>Elson, Sarah L.</creatorcontrib><creatorcontrib>Stoller, James K.</creatorcontrib><creatorcontrib>Agee, Michelle</creatorcontrib><creatorcontrib>Aslibekyan, Stella</creatorcontrib><creatorcontrib>Auton, Adam</creatorcontrib><creatorcontrib>Babalola, Elizabeth</creatorcontrib><creatorcontrib>Bell, Robert K.</creatorcontrib><creatorcontrib>Bielenberg, Jessica</creatorcontrib><creatorcontrib>Bryc, Katarzyna</creatorcontrib><creatorcontrib>Bullis, Emily</creatorcontrib><creatorcontrib>Cameron, Briana</creatorcontrib><creatorcontrib>Coker, Daniella</creatorcontrib><creatorcontrib>Partida, Gabriel Cuellar</creatorcontrib><creatorcontrib>Dhamija, Devika</creatorcontrib><creatorcontrib>Das, Sayantan</creatorcontrib><creatorcontrib>Elson, Sarah L.</creatorcontrib><creatorcontrib>Filshtein, Teresa</creatorcontrib><creatorcontrib>Fletez-Brant, Kipper</creatorcontrib><creatorcontrib>Fontanillas, Pierre</creatorcontrib><creatorcontrib>Freyman, Will</creatorcontrib><creatorcontrib>Gandhi, Pooja M.</creatorcontrib><creatorcontrib>Heilbron, Karl</creatorcontrib><creatorcontrib>Hicks, Barry</creatorcontrib><creatorcontrib>Hinds, David A.</creatorcontrib><creatorcontrib>Huber, Karen E.</creatorcontrib><creatorcontrib>Jewett, Ethan M.</creatorcontrib><creatorcontrib>Jiang, Yunxuan</creatorcontrib><creatorcontrib>Kleinman, Aaron</creatorcontrib><creatorcontrib>Kukar, Katelyn</creatorcontrib><creatorcontrib>Lane, Vanessa A.</creatorcontrib><creatorcontrib>Lin, Keng-Han</creatorcontrib><creatorcontrib>Lowe, Maya</creatorcontrib><creatorcontrib>Luff, Marie K.</creatorcontrib><creatorcontrib>McCreight, Jennifer C.</creatorcontrib><creatorcontrib>McIntyre, Matthew H.</creatorcontrib><creatorcontrib>McManus, Kimberly F.</creatorcontrib><creatorcontrib>Micheletti, Steven J.</creatorcontrib><creatorcontrib>Moreno, Meghan E.</creatorcontrib><creatorcontrib>Mountain, Joanna L.</creatorcontrib><creatorcontrib>Mozaffari, Sahar V.</creatorcontrib><creatorcontrib>Nandakumar, Priyanka</creatorcontrib><creatorcontrib>Noblin, Elizabeth S.</creatorcontrib><creatorcontrib>O’Connell, Jared</creatorcontrib><creatorcontrib>Petrakovitz, Aaron A.</creatorcontrib><creatorcontrib>Poznik, G. David</creatorcontrib><creatorcontrib>Schumacher, Morgan</creatorcontrib><creatorcontrib>Shastri, Anjali J.</creatorcontrib><creatorcontrib>Shelton, Janie F.</creatorcontrib><creatorcontrib>Shi, Jingchunzi</creatorcontrib><creatorcontrib>Shringarpure, Suyash</creatorcontrib><creatorcontrib>Tian, Chao</creatorcontrib><creatorcontrib>Tran, Vinh</creatorcontrib><creatorcontrib>Tung, Joyce Y.</creatorcontrib><creatorcontrib>Wang, Xin</creatorcontrib><creatorcontrib>Wang, Wei</creatorcontrib><creatorcontrib>Weldon, Catherine H.</creatorcontrib><creatorcontrib>Wilton, Peter</creatorcontrib><creatorcontrib>23andMe Research Team</creatorcontrib><title>Prevalence of Alpha-1 Antitrypsin Deficiency, Self-Reported Behavior Change, and Health Care Engagement Among Direct-to-Consumer Recipients of a Personalized Genetic Risk Report</title><title>Chest</title><addtitle>Chest</addtitle><description>Alpha-1 antitrypsin deficiency (AATD) is an autosomal co-dominant condition that predisposes to emphysema, cirrhosis, panniculitis, and vasculitis. Underrecognition has prompted efforts to enhance early detection and testing of at-risk individuals. Direct-to-consumer (DTC) genetic testing represents an additional method of detection.
The study addressed three questions: (1) Does a DTC testing service identify previously undetected individuals with AATD? (2) What was the interval between initial AATD-related symptoms and initial diagnosis of AATD in such individuals? and (3) What was the behavioral impact of learning about a new diagnosis of AATD through a DTC test?
In this cross-sectional study, 195,014 individuals responded to a survey within the 23andMe, Inc. research platform.
Among 195,014 study participants, the allele frequency for the PI∗S and PI∗Z AATD variants was 21.6% (6.5% for PI∗Z and 15.1% for PI∗S); 0.63% were PI∗ZZ, half of whom reported having a physician confirm the diagnosis. Approximately 27% of those with physician-diagnosed AATD reported first becoming aware of AATD through the DTC test. Among those newly aware participants, the diagnostic delay interval was 22.3 years. Participants frequently shared their DTC test results with health care providers (HCPs) and the reported impact of learning a diagnosis of AATD was high. For example, 51.1% of PI∗ZZ individuals shared their DTC result with an HCP. The OR for PI∗ZZ smokers to report smoking reduction as a result of receiving the DTC result was 1.7 (95% CI = 1.4-2.2) compared with those without a Z allele and for reduced alcohol consumption this was 4.0 (95% CI = 2.6-5.9).
In this largest available report on DTC testing for AATD, this test, in combination with clinical follow-up, can help to identify previously undiagnosed AATD patients. Moreover, receipt of the DTC AATD report was associated with positive behavior change, especially among those with risk variants.
[Display omitted]</description><subject>AATD</subject><subject>alpha 1-Antitrypsin Deficiency - epidemiology</subject><subject>alpha 1-Antitrypsin Deficiency - genetics</subject><subject>alpha-1 antitrypsin deficiency</subject><subject>consumer genomics</subject><subject>direct-to-consumer</subject><subject>Direct-To-Consumer Screening and Testing</subject><subject>Female</subject><subject>Genetic Testing</subject><subject>Genotype</subject><subject>Humans</subject><subject>lung disease</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Prevalence</subject><subject>rare disease</subject><subject>Self Report</subject><subject>SERPINA1</subject><issn>0012-3692</issn><issn>1931-3543</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc9uEzEQhy0EoqHwBEjIRw7dxV7vPx84hG1pkSpRBThbXns2cdi1t7YTKbwVb4iTFI5cbFn6zXzj-RB6S0lOCa0_bHO1gRDzghQ0JzwnJX2GFpQzmrGqZM_RghBaZKzmxQV6FcKWpDfl9Ut0wcq6qquiWqDfDx72cgSrALsBL8d5IzOKlzaa6A9zMBZfw2CUSYnDFf4G45CtYHY-gsafYCP3xnncbaRdwxWWVuM7kGPc4E56wDd2LdcwgY14OTm7xtfGg4pZdFnnbNhN4PEKlJlT-xiOA0j8AD44K0fzKxFuwUI0Cq9M-InP3NfoxSDHAG-e7kv04_PN9-4uu_96-6Vb3meqJGXM6pI2JVGkbzRp6TDwXirWD03LdcsbVhNoOdO6L3Q6WtDQElmUlDS8LKisOLtE7899Z-8ed2nRYjJBwThKC24XRFG1jBUJU6coO0eVdyF4GMTszST9QVAijq7EVpxciaMrQbhIrlLVuyfArp9A_6v5KycFPp4DkL65N-BFOHkAfdqi0M78F_AHlm6oPw</recordid><startdate>202202</startdate><enddate>202202</enddate><creator>Ashenhurst, James R.</creator><creator>Nhan, Hoang</creator><creator>Shelton, Janie F.</creator><creator>Wu, Shirley</creator><creator>Tung, Joyce Y.</creator><creator>Elson, Sarah L.</creator><creator>Stoller, James K.</creator><creator>Agee, Michelle</creator><creator>Aslibekyan, Stella</creator><creator>Auton, Adam</creator><creator>Babalola, Elizabeth</creator><creator>Bell, Robert K.</creator><creator>Bielenberg, Jessica</creator><creator>Bryc, Katarzyna</creator><creator>Bullis, Emily</creator><creator>Cameron, Briana</creator><creator>Coker, Daniella</creator><creator>Partida, Gabriel Cuellar</creator><creator>Dhamija, Devika</creator><creator>Das, Sayantan</creator><creator>Elson, Sarah L.</creator><creator>Filshtein, Teresa</creator><creator>Fletez-Brant, Kipper</creator><creator>Fontanillas, Pierre</creator><creator>Freyman, Will</creator><creator>Gandhi, Pooja M.</creator><creator>Heilbron, Karl</creator><creator>Hicks, Barry</creator><creator>Hinds, David A.</creator><creator>Huber, Karen E.</creator><creator>Jewett, Ethan M.</creator><creator>Jiang, Yunxuan</creator><creator>Kleinman, Aaron</creator><creator>Kukar, Katelyn</creator><creator>Lane, Vanessa A.</creator><creator>Lin, Keng-Han</creator><creator>Lowe, Maya</creator><creator>Luff, Marie K.</creator><creator>McCreight, Jennifer C.</creator><creator>McIntyre, Matthew H.</creator><creator>McManus, Kimberly F.</creator><creator>Micheletti, Steven J.</creator><creator>Moreno, Meghan E.</creator><creator>Mountain, Joanna L.</creator><creator>Mozaffari, Sahar V.</creator><creator>Nandakumar, Priyanka</creator><creator>Noblin, Elizabeth S.</creator><creator>O’Connell, Jared</creator><creator>Petrakovitz, Aaron A.</creator><creator>Poznik, G. David</creator><creator>Schumacher, Morgan</creator><creator>Shastri, Anjali J.</creator><creator>Shelton, Janie F.</creator><creator>Shi, Jingchunzi</creator><creator>Shringarpure, Suyash</creator><creator>Tian, Chao</creator><creator>Tran, Vinh</creator><creator>Tung, Joyce Y.</creator><creator>Wang, Xin</creator><creator>Wang, Wei</creator><creator>Weldon, Catherine H.</creator><creator>Wilton, Peter</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202202</creationdate><title>Prevalence of Alpha-1 Antitrypsin Deficiency, Self-Reported Behavior Change, and Health Care Engagement Among Direct-to-Consumer Recipients of a Personalized Genetic Risk Report</title><author>Ashenhurst, James R. ; Nhan, Hoang ; Shelton, Janie F. ; Wu, Shirley ; Tung, Joyce Y. ; Elson, Sarah L. ; Stoller, James K. ; Agee, Michelle ; Aslibekyan, Stella ; Auton, Adam ; Babalola, Elizabeth ; Bell, Robert K. ; Bielenberg, Jessica ; Bryc, Katarzyna ; Bullis, Emily ; Cameron, Briana ; Coker, Daniella ; Partida, Gabriel Cuellar ; Dhamija, Devika ; Das, Sayantan ; Elson, Sarah L. ; Filshtein, Teresa ; Fletez-Brant, Kipper ; Fontanillas, Pierre ; Freyman, Will ; Gandhi, Pooja M. ; Heilbron, Karl ; Hicks, Barry ; Hinds, David A. ; Huber, Karen E. ; Jewett, Ethan M. ; Jiang, Yunxuan ; Kleinman, Aaron ; Kukar, Katelyn ; Lane, Vanessa A. ; Lin, Keng-Han ; Lowe, Maya ; Luff, Marie K. ; McCreight, Jennifer C. ; McIntyre, Matthew H. ; McManus, Kimberly F. ; Micheletti, Steven J. ; Moreno, Meghan E. ; Mountain, Joanna L. ; Mozaffari, Sahar V. ; Nandakumar, Priyanka ; Noblin, Elizabeth S. ; O’Connell, Jared ; Petrakovitz, Aaron A. ; Poznik, G. David ; Schumacher, Morgan ; Shastri, Anjali J. ; Shelton, Janie F. ; Shi, Jingchunzi ; Shringarpure, Suyash ; Tian, Chao ; Tran, Vinh ; Tung, Joyce Y. ; Wang, Xin ; Wang, Wei ; Weldon, Catherine H. ; Wilton, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-641740c0b7d081ff9bac3bf789d897360e893ddb2dddb8ede80a241079421a593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>AATD</topic><topic>alpha 1-Antitrypsin Deficiency - epidemiology</topic><topic>alpha 1-Antitrypsin Deficiency - genetics</topic><topic>alpha-1 antitrypsin deficiency</topic><topic>consumer genomics</topic><topic>direct-to-consumer</topic><topic>Direct-To-Consumer Screening and Testing</topic><topic>Female</topic><topic>Genetic Testing</topic><topic>Genotype</topic><topic>Humans</topic><topic>lung disease</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Prevalence</topic><topic>rare disease</topic><topic>Self Report</topic><topic>SERPINA1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ashenhurst, James R.</creatorcontrib><creatorcontrib>Nhan, Hoang</creatorcontrib><creatorcontrib>Shelton, Janie F.</creatorcontrib><creatorcontrib>Wu, Shirley</creatorcontrib><creatorcontrib>Tung, Joyce Y.</creatorcontrib><creatorcontrib>Elson, Sarah L.</creatorcontrib><creatorcontrib>Stoller, James K.</creatorcontrib><creatorcontrib>Agee, Michelle</creatorcontrib><creatorcontrib>Aslibekyan, Stella</creatorcontrib><creatorcontrib>Auton, Adam</creatorcontrib><creatorcontrib>Babalola, Elizabeth</creatorcontrib><creatorcontrib>Bell, Robert K.</creatorcontrib><creatorcontrib>Bielenberg, Jessica</creatorcontrib><creatorcontrib>Bryc, Katarzyna</creatorcontrib><creatorcontrib>Bullis, Emily</creatorcontrib><creatorcontrib>Cameron, Briana</creatorcontrib><creatorcontrib>Coker, Daniella</creatorcontrib><creatorcontrib>Partida, Gabriel Cuellar</creatorcontrib><creatorcontrib>Dhamija, Devika</creatorcontrib><creatorcontrib>Das, Sayantan</creatorcontrib><creatorcontrib>Elson, Sarah L.</creatorcontrib><creatorcontrib>Filshtein, Teresa</creatorcontrib><creatorcontrib>Fletez-Brant, Kipper</creatorcontrib><creatorcontrib>Fontanillas, Pierre</creatorcontrib><creatorcontrib>Freyman, Will</creatorcontrib><creatorcontrib>Gandhi, Pooja M.</creatorcontrib><creatorcontrib>Heilbron, Karl</creatorcontrib><creatorcontrib>Hicks, Barry</creatorcontrib><creatorcontrib>Hinds, David A.</creatorcontrib><creatorcontrib>Huber, Karen E.</creatorcontrib><creatorcontrib>Jewett, Ethan M.</creatorcontrib><creatorcontrib>Jiang, Yunxuan</creatorcontrib><creatorcontrib>Kleinman, Aaron</creatorcontrib><creatorcontrib>Kukar, Katelyn</creatorcontrib><creatorcontrib>Lane, Vanessa A.</creatorcontrib><creatorcontrib>Lin, Keng-Han</creatorcontrib><creatorcontrib>Lowe, Maya</creatorcontrib><creatorcontrib>Luff, Marie K.</creatorcontrib><creatorcontrib>McCreight, Jennifer C.</creatorcontrib><creatorcontrib>McIntyre, Matthew H.</creatorcontrib><creatorcontrib>McManus, Kimberly F.</creatorcontrib><creatorcontrib>Micheletti, Steven J.</creatorcontrib><creatorcontrib>Moreno, Meghan E.</creatorcontrib><creatorcontrib>Mountain, Joanna L.</creatorcontrib><creatorcontrib>Mozaffari, Sahar V.</creatorcontrib><creatorcontrib>Nandakumar, Priyanka</creatorcontrib><creatorcontrib>Noblin, Elizabeth S.</creatorcontrib><creatorcontrib>O’Connell, Jared</creatorcontrib><creatorcontrib>Petrakovitz, Aaron A.</creatorcontrib><creatorcontrib>Poznik, G. David</creatorcontrib><creatorcontrib>Schumacher, Morgan</creatorcontrib><creatorcontrib>Shastri, Anjali J.</creatorcontrib><creatorcontrib>Shelton, Janie F.</creatorcontrib><creatorcontrib>Shi, Jingchunzi</creatorcontrib><creatorcontrib>Shringarpure, Suyash</creatorcontrib><creatorcontrib>Tian, Chao</creatorcontrib><creatorcontrib>Tran, Vinh</creatorcontrib><creatorcontrib>Tung, Joyce Y.</creatorcontrib><creatorcontrib>Wang, Xin</creatorcontrib><creatorcontrib>Wang, Wei</creatorcontrib><creatorcontrib>Weldon, Catherine H.</creatorcontrib><creatorcontrib>Wilton, Peter</creatorcontrib><creatorcontrib>23andMe Research Team</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chest</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ashenhurst, James R.</au><au>Nhan, Hoang</au><au>Shelton, Janie F.</au><au>Wu, Shirley</au><au>Tung, Joyce Y.</au><au>Elson, Sarah L.</au><au>Stoller, James K.</au><au>Agee, Michelle</au><au>Aslibekyan, Stella</au><au>Auton, Adam</au><au>Babalola, Elizabeth</au><au>Bell, Robert K.</au><au>Bielenberg, Jessica</au><au>Bryc, Katarzyna</au><au>Bullis, Emily</au><au>Cameron, Briana</au><au>Coker, Daniella</au><au>Partida, Gabriel Cuellar</au><au>Dhamija, Devika</au><au>Das, Sayantan</au><au>Elson, Sarah L.</au><au>Filshtein, Teresa</au><au>Fletez-Brant, Kipper</au><au>Fontanillas, Pierre</au><au>Freyman, Will</au><au>Gandhi, Pooja M.</au><au>Heilbron, Karl</au><au>Hicks, Barry</au><au>Hinds, David A.</au><au>Huber, Karen E.</au><au>Jewett, Ethan M.</au><au>Jiang, Yunxuan</au><au>Kleinman, Aaron</au><au>Kukar, Katelyn</au><au>Lane, Vanessa A.</au><au>Lin, Keng-Han</au><au>Lowe, Maya</au><au>Luff, Marie K.</au><au>McCreight, Jennifer C.</au><au>McIntyre, Matthew H.</au><au>McManus, Kimberly F.</au><au>Micheletti, Steven J.</au><au>Moreno, Meghan E.</au><au>Mountain, Joanna L.</au><au>Mozaffari, Sahar V.</au><au>Nandakumar, Priyanka</au><au>Noblin, Elizabeth S.</au><au>O’Connell, Jared</au><au>Petrakovitz, Aaron A.</au><au>Poznik, G. David</au><au>Schumacher, Morgan</au><au>Shastri, Anjali J.</au><au>Shelton, Janie F.</au><au>Shi, Jingchunzi</au><au>Shringarpure, Suyash</au><au>Tian, Chao</au><au>Tran, Vinh</au><au>Tung, Joyce Y.</au><au>Wang, Xin</au><au>Wang, Wei</au><au>Weldon, Catherine H.</au><au>Wilton, Peter</au><aucorp>23andMe Research Team</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevalence of Alpha-1 Antitrypsin Deficiency, Self-Reported Behavior Change, and Health Care Engagement Among Direct-to-Consumer Recipients of a Personalized Genetic Risk Report</atitle><jtitle>Chest</jtitle><addtitle>Chest</addtitle><date>2022-02</date><risdate>2022</risdate><volume>161</volume><issue>2</issue><spage>373</spage><epage>381</epage><pages>373-381</pages><issn>0012-3692</issn><eissn>1931-3543</eissn><abstract>Alpha-1 antitrypsin deficiency (AATD) is an autosomal co-dominant condition that predisposes to emphysema, cirrhosis, panniculitis, and vasculitis. Underrecognition has prompted efforts to enhance early detection and testing of at-risk individuals. Direct-to-consumer (DTC) genetic testing represents an additional method of detection.
The study addressed three questions: (1) Does a DTC testing service identify previously undetected individuals with AATD? (2) What was the interval between initial AATD-related symptoms and initial diagnosis of AATD in such individuals? and (3) What was the behavioral impact of learning about a new diagnosis of AATD through a DTC test?
In this cross-sectional study, 195,014 individuals responded to a survey within the 23andMe, Inc. research platform.
Among 195,014 study participants, the allele frequency for the PI∗S and PI∗Z AATD variants was 21.6% (6.5% for PI∗Z and 15.1% for PI∗S); 0.63% were PI∗ZZ, half of whom reported having a physician confirm the diagnosis. Approximately 27% of those with physician-diagnosed AATD reported first becoming aware of AATD through the DTC test. Among those newly aware participants, the diagnostic delay interval was 22.3 years. Participants frequently shared their DTC test results with health care providers (HCPs) and the reported impact of learning a diagnosis of AATD was high. For example, 51.1% of PI∗ZZ individuals shared their DTC result with an HCP. The OR for PI∗ZZ smokers to report smoking reduction as a result of receiving the DTC result was 1.7 (95% CI = 1.4-2.2) compared with those without a Z allele and for reduced alcohol consumption this was 4.0 (95% CI = 2.6-5.9).
In this largest available report on DTC testing for AATD, this test, in combination with clinical follow-up, can help to identify previously undiagnosed AATD patients. Moreover, receipt of the DTC AATD report was associated with positive behavior change, especially among those with risk variants.
[Display omitted]</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>34656525</pmid><doi>10.1016/j.chest.2021.09.041</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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ispartof | Chest, 2022-02, Vol.161 (2), p.373-381 |
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subjects | AATD alpha 1-Antitrypsin Deficiency - epidemiology alpha 1-Antitrypsin Deficiency - genetics alpha-1 antitrypsin deficiency consumer genomics direct-to-consumer Direct-To-Consumer Screening and Testing Female Genetic Testing Genotype Humans lung disease Male Middle Aged Prevalence rare disease Self Report SERPINA1 |
title | Prevalence of Alpha-1 Antitrypsin Deficiency, Self-Reported Behavior Change, and Health Care Engagement Among Direct-to-Consumer Recipients of a Personalized Genetic Risk Report |
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