TY - JOUR
T1 - The global, regional, and national burden of benign prostatic hyperplasia in 204 countries and territories from 2000 to 2019
T2 - a systematic analysis for the Global Burden of Disease Study 2019
AU - GBD 2019 Benign Prostatic Hyperplasia Collaborators
AU - Awedew, Atalel Fentahun
AU - Han, Hannah
AU - Abbasi, Behzad
AU - Abbasi-Kangevari, Mohsen
AU - Ahmed, Muktar Beshir
AU - Almidani, Omar
AU - Amini, Erfan
AU - Arabloo, Jalal
AU - Argaw, Ayele Mamo
AU - Athari, Seyyed Shamsadin
AU - Atlaw, Daniel
AU - Banach, Maciej
AU - Barrow, Amadou
AU - Bhagavathula, Akshaya Srikanth
AU - Bhojaraja, Vijayalakshmi S.
AU - Bikbov, Boris
AU - Bodicha, Belay Boda Abule
AU - Butt, Nadeem Shafique
AU - Caetano dos Santos, Florentino Luciano
AU - Dadras, Omid
AU - Dai, Xiaochen
AU - Doan, Linh Phuong
AU - Eftekharzadeh, Sahar
AU - Fatehizadeh, Ali
AU - Garg, Tushar
AU - Gebremeskel, Teferi Gebru
AU - Getachew, Motuma Erena
AU - Ghamari, Seyyed Hadi
AU - Gilani, Syed Amir
AU - Golechha, Mahaveer
AU - Gupta, Veer Bala
AU - Gupta, Vivek Kumar
AU - Hay, Simon I.
AU - Hosseini, Mohammad Salar
AU - Hosseinzadeh, Mehdi
AU - Humayun, Ayesha
AU - Ilic, Irena M.
AU - Ilic, Milena D.
AU - Ismail, Nahlah Elkudssiah
AU - Jakovljevic, Mihajlo
AU - Jayaram, Shubha
AU - Jazayeri, Seyed Behzad
AU - Jema, Alelign Tasew
AU - Kabir, Ali
AU - Karaye, Ibraheem M.
AU - Khader, Yousef Saleh
AU - Khan, Ejaz Ahmad
AU - Landires, Iván
AU - Lee, Sang woong
AU - Lee, Shaun Wen Huey
AU - Lim, Stephen S.
AU - Lobo, Stany W.
AU - Majeed, Azeem
AU - Malekpour, Mohammad Reza
AU - Malih, Narges
AU - Malik, Ahmad Azam
AU - Mehrabi Nasab, Entezar
AU - Mestrovic, Tomislav
AU - Michalek, Irmina Maria
AU - Mihrtie, Gedefaye Nibret
AU - Mirza-Aghazadeh-Attari, Mohammad
AU - Misganaw, Awoke Temesgen
AU - Mokdad, Ali H.
AU - Molokhia, Mariam
AU - Murray, Christopher J.L.
AU - Narasimha Swamy, Sreenivas
AU - Nguyen, Son Hoang
AU - Nowroozi, Ali
AU - Nuñez-Samudio, Virginia
AU - Owolabi, Mayowa O.
AU - Pawar, Shrikant
AU - Perico, Norberto
AU - Rawaf, David Laith
AU - Rawaf, Salman
AU - Rawassizadeh, Reza
AU - Remuzzi, Giuseppe
AU - Sahebkar, Amirhossein
AU - Sampath, Chethan
AU - Shetty, Jeevan K.
AU - Sibhat, Migbar Mekonnen
AU - Singh, Jasvinder A.
AU - Tan, Ker Kan
AU - Temesgen, Gebremaryam
AU - Tolani, Musliu Adetola
AU - Tovani-Palone, Marcos Roberto
AU - Valadan Tahbaz, Sahel
AU - Valizadeh, Rohollah
AU - Vo, Bay
AU - Vu, Linh Gia
AU - Yang, Lin
AU - Yazdanpanah, Fereshteh
AU - Yigit, Arzu
AU - Yiğit, Vahit
AU - Yunusa, Ismaeel
AU - Zahir, Mazyar
AU - Vos, Theo
AU - Dirac, M. Ashworth
PY - 2022/11
Y1 - 2022/11
N2 - Background: Benign prostatic hyperplasia is a common urological disease affecting older men worldwide, but comprehensive data about the global, regional, and national burden of benign prostatic hyperplasia and its trends over time are scarce. As part of the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019, we estimated global trends in, and prevalence of, benign prostatic hyperplasia and disability-adjusted life-years (DALYs) due to benign prostatic hyperplasia, in 21 regions and 204 countries and territories from 2000 to 2019. Methods: This study was conducted with GBD 2019 analytical and modelling strategies. Primary prevalence data came from claims from three countries and from hospital inpatient encounters from 45 locations. A Bayesian meta-regression modelling tool, DisMod-MR version 2.1, was used to estimate the age-specific, location-specific, and year-specific prevalence of benign prostatic hyperplasia. Age-standardised prevalence was calculated by the direct method using the GBD reference population. Years lived with disability (YLDs) due to benign prostatic hyperplasia were estimated by multiplying the disability weight by the symptomatic proportion of the prevalence of benign prostatic hyperplasia. Because we did not estimate years of life lost associated with benign prostatic hyperplasia, disability-adjusted life-years (DALYs) equalled YLDs. The final estimates were compared across Socio-demographic Index (SDI) quintiles. The 95% uncertainty intervals (UIs) were estimated as the 25th and 975th of 1000 ordered draws from a bootstrap distribution. Findings: Globally, there were 94·0 million (95% UI 73·2 to 118) prevalent cases of benign prostatic hyperplasia in 2019, compared with 51·1 million (43·1 to 69·3) cases in 2000. The age-standardised prevalence of benign prostatic hyperplasia was 2480 (1940 to 3090) per 100 000 people. Although the global number of prevalent cases increased by 70·5% (68·6 to 72·7) between 2000 and 2019, the global age-standardised prevalence remained stable (–0·770% [–1·56 to 0·0912]). The age-standardised prevalence in 2019 ranged from 6480 (5130 to 8080) per 100 000 in eastern Europe to 987 (732 to 1320) per 100 000 in north Africa and the Middle East. All five SDI quintiles observed an increase in the absolute DALY burden between 2000 and 2019. The most rapid increases in the absolute DALY burden were seen in the middle SDI quintile (94·7% [91·8 to 97·6]), the low-middle SDI quintile (77·3% [74·1 to 81·2]), and the low SDI quintile (77·7% [72·9 to 83·2]). Between 2000 and 2019, age-standardised DALY rates changed less, but the three lower SDI quintiles (low, low-middle, and middle) saw small increases, and the two higher SDI quintiles (high and high-middle SDI) saw small decreases. Interpretation: The absolute burden of benign prostatic hyperplasia is rising at an alarming rate in most of the world, particularly in low-income and middle-income countries that are currently undergoing rapid demographic and epidemiological changes. As more people are living longer worldwide, the absolute burden of benign prostatic hyperplasia is expected to continue to rise in the coming years, highlighting the importance of monitoring and planning for future health system strain. Funding: Bill & Melinda Gates Foundation. Translation: For the Amharic translation of the abstract see Supplementary Materials section.
AB - Background: Benign prostatic hyperplasia is a common urological disease affecting older men worldwide, but comprehensive data about the global, regional, and national burden of benign prostatic hyperplasia and its trends over time are scarce. As part of the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019, we estimated global trends in, and prevalence of, benign prostatic hyperplasia and disability-adjusted life-years (DALYs) due to benign prostatic hyperplasia, in 21 regions and 204 countries and territories from 2000 to 2019. Methods: This study was conducted with GBD 2019 analytical and modelling strategies. Primary prevalence data came from claims from three countries and from hospital inpatient encounters from 45 locations. A Bayesian meta-regression modelling tool, DisMod-MR version 2.1, was used to estimate the age-specific, location-specific, and year-specific prevalence of benign prostatic hyperplasia. Age-standardised prevalence was calculated by the direct method using the GBD reference population. Years lived with disability (YLDs) due to benign prostatic hyperplasia were estimated by multiplying the disability weight by the symptomatic proportion of the prevalence of benign prostatic hyperplasia. Because we did not estimate years of life lost associated with benign prostatic hyperplasia, disability-adjusted life-years (DALYs) equalled YLDs. The final estimates were compared across Socio-demographic Index (SDI) quintiles. The 95% uncertainty intervals (UIs) were estimated as the 25th and 975th of 1000 ordered draws from a bootstrap distribution. Findings: Globally, there were 94·0 million (95% UI 73·2 to 118) prevalent cases of benign prostatic hyperplasia in 2019, compared with 51·1 million (43·1 to 69·3) cases in 2000. The age-standardised prevalence of benign prostatic hyperplasia was 2480 (1940 to 3090) per 100 000 people. Although the global number of prevalent cases increased by 70·5% (68·6 to 72·7) between 2000 and 2019, the global age-standardised prevalence remained stable (–0·770% [–1·56 to 0·0912]). The age-standardised prevalence in 2019 ranged from 6480 (5130 to 8080) per 100 000 in eastern Europe to 987 (732 to 1320) per 100 000 in north Africa and the Middle East. All five SDI quintiles observed an increase in the absolute DALY burden between 2000 and 2019. The most rapid increases in the absolute DALY burden were seen in the middle SDI quintile (94·7% [91·8 to 97·6]), the low-middle SDI quintile (77·3% [74·1 to 81·2]), and the low SDI quintile (77·7% [72·9 to 83·2]). Between 2000 and 2019, age-standardised DALY rates changed less, but the three lower SDI quintiles (low, low-middle, and middle) saw small increases, and the two higher SDI quintiles (high and high-middle SDI) saw small decreases. Interpretation: The absolute burden of benign prostatic hyperplasia is rising at an alarming rate in most of the world, particularly in low-income and middle-income countries that are currently undergoing rapid demographic and epidemiological changes. As more people are living longer worldwide, the absolute burden of benign prostatic hyperplasia is expected to continue to rise in the coming years, highlighting the importance of monitoring and planning for future health system strain. Funding: Bill & Melinda Gates Foundation. Translation: For the Amharic translation of the abstract see Supplementary Materials section.
KW - benign prostatic hyperplasia
KW - Global Burden of Disease Study 2019
KW - systematic analysis
KW - Bayesian meta-regression modelling tool
UR - http://www.scopus.com/inward/record.url?scp=85141746748&partnerID=8YFLogxK
U2 - 10.1016/S2666-7568(22)00213-6
DO - 10.1016/S2666-7568(22)00213-6
M3 - Article
AN - SCOPUS:85141746748
SN - 2666-7568
VL - 3
SP - e754-e776
JO - The Lancet Healthy Longevity
JF - The Lancet Healthy Longevity
IS - 11
ER -