TY - JOUR
T1 - Sex Differences in Diagnosis, Treatment, and Cardiovascular Outcomes in Homozygous Familial Hypercholesterolemia
AU - the Homozygous Familial Hypercholesterolemia International Clinical Collaborators
AU - Mulder, Janneke W.C.M.
AU - Tromp, Tycho R.
AU - Al-Khnifsawi, Mutaz
AU - Blom, Dirk J.
AU - Chlebus, Krysztof
AU - Cuchel, Marina
AU - D'Erasmo, Laura
AU - Gallo, Antonio
AU - Hovingh, G. Kees
AU - Kim, Ngoc Thanh
AU - Long, Jiang
AU - Raal, Frederick J.
AU - Schonck, Willemijn A.M.
AU - Soran, Handrean
AU - Truong, Thanh Huong
AU - Boersma, Eric
AU - Roeters van Lennep, Jeanine E.
AU - Alareedh, Mohammed D.
AU - Alieva, Rano
AU - Allevi, Massimiliano
AU - Altunkeser, Bulent B.
AU - Al-Waili, Khalid
AU - Al-Zamili, Ali F.
AU - Arca, Marcello
AU - Atzori, Luigi
AU - Averna, Maurizio
AU - Ayesh, Mahmoud H.
AU - Azar, Sami T.
AU - Banderali, Giuseppe
AU - Baratta, Francesco
AU - Bartuli, Andrea
AU - Béliard, Sophie
AU - Bianconi, Vanessa
AU - Bini, Simone
AU - Thani, Khalid Bin
AU - Bitar, Fadi F.
AU - Blaha, Vladimir
AU - Bonomo, Katia
AU - Bourbon, Mafalda
AU - Branchi, Adriana
AU - Brothers, Julie A.
AU - Bruckert, Eric
AU - Brunham, Liam R.
AU - Bruzzi, Patrizia
AU - Bucci, Marco
AU - Buonuomo, Paola S.
AU - Calabrò, Paolo
AU - Calandra, Sebastiano
AU - Carubbi, Francesca
AU - Cassiman, David
AU - Casula, Manuela
AU - Catapano, Alberico L.
AU - Cavalot, Franco
AU - Cefalù, Angelo B.
AU - Cesaro, Arturo
AU - Ceska, Richard
AU - Charng, Min Ji
AU - Cipollone, Francesco
AU - Cohen, Hofit
AU - D'Addato, Sergio
AU - Dal Pino, Beatrice
AU - Dann, Eldad J.
AU - Defesche, Joep C.
AU - Del Ben, Maria
AU - Demircioglu, Sinan
AU - Descamps, Olivier S.
AU - Di Costanzo, Alessia
AU - Di Taranto, Maria D.
AU - Do, Doan Loi
AU - Durst, Ronen
AU - Dvorakova, Jana
AU - Ebenbichler, Christoph F.
AU - Elis, Avishay
AU - Emil, Sameh
AU - Ezhov, Marat V.
AU - Fahed, Akl C.
AU - Fasano, Tommaso
AU - Ferri, Claudio
AU - Fogacci, Federica
AU - Formisano, Elena
AU - Fortunato, Giuliana
AU - Francis, Gordon A.
AU - Freiberger, Tomas
AU - Galimberti, Federica
AU - Gaspar, Isabel M.
AU - Genest, Jacques
AU - Gentile, Marco
AU - Giammanco, Antonina
AU - Gokce, Cumali
AU - Greber-Platzer, Susanne
AU - Grigore, Liliana
AU - Groselj, Urh
AU - Harada-Shiba, Mariko
AU - Hartgers, Merel L.
AU - Hegele, Robert A.
AU - Horak, Pavel
AU - Hori, Mika
AU - Hudgins, Lisa C.
AU - Hussein, Osama
AU - Iannuzzo, Gabriella
AU - Ilhan, Osman
AU - Iughetti, Lorenzo
AU - Kayikcioglu, Meral
AU - Kaynar, Leyla G.
AU - Kennedy, Brooke A.
AU - Khovidhunkit, Weerapan
AU - Kolovou, Genovefa
AU - Kose, Melis
AU - Kuku, Irfan
AU - Kurtoglu, Erdal
AU - Lalic, Katarina S.
AU - Le, Hong An
AU - Le, Thanh Tung
AU - Leitersdorf, Eran
AU - Liberopoulos, Evangelos
AU - Lyons, Alexander R.M.
AU - Madriz, Ramón
AU - Mandraffino, Giuseppe
AU - Mäser, Martin
AU - Mehta, Roopa
AU - Mitchenko, Olena
AU - Mombelli, Giuliana
AU - Montalcini, Tiziana
AU - Morace, Carmela
AU - Moubarak, Elie M.
AU - Muntoni, Sandro
AU - Naguib, Tarek A.
AU - Nascimbeni, Fabio
AU - Nawawi, Hapizah
AU - Nemer, Georges
AU - Nguyen, Mai Ngoc T.
AU - Notargiacomo, Serena
AU - Okutan, Harika
AU - Ozcebe, Osman I.
AU - Pang, Jing
AU - Passaro, Angelina
AU - Pavanello, Chiara
AU - Pecchioli, Lorenzo
AU - Pecchioli, Valerio
AU - Pederiva, Cristina
AU - Pekkolay, Zafer
AU - Pellegatta, Fabio
AU - Piro, Salvatore
AU - Pirro, Matteo
AU - Pisciotta, Livia
AU - Pujia, Arturo
AU - Ray, Kausik K.
AU - Reda, Ashraf
AU - Reijman, M. Doortje
AU - Reiner, Željko
AU - Rhadi, Sabah H.
AU - Rizzi, Luigi
AU - Romandini, Alessandra
AU - Ruel, Isabelle
AU - Rymen, Daisy
AU - Sadiq, Fouzia
AU - Sag, Saim
AU - Salcioglu, Osman Z.
AU - Santos, Raul D.
AU - Sanz, Juana M.
AU - Sarzani, Riccardo
AU - Sbrana, Francesco
AU - Schurr, Daniel
AU - Scicali, Roberto
AU - Setia, Nitika
AU - Shaghee, Foaad K.
AU - Shek, Aleksandr
AU - Sherman, Mark H.
AU - Soska, Vladimir
AU - Stevens, Christophe A.T.
AU - Stroes, Erik S.G.
AU - Stulnig, Thomas M.
AU - Suppressa, Patrizia
AU - Susekov, Andrey V.
AU - Tarugi, Patrizia
AU - Temizhan, Ahmet
AU - Tichy, Lukas
AU - Trenti, Chiara
AU - Urbanek, Robin
AU - Vallejo-Vaz, Antonio J.
AU - Vaverkova, Helena
AU - Verma, Ishwar C.
AU - Vrablik, Michal
AU - Wang, Luya
AU - Watts, Gerald F.
AU - Werba, José P.
AU - Wiegman, Albert
AU - Witters, Peter
AU - Yenercag, Mustafa
AU - Yilmaz, Mehmet
AU - Yasar, Hamiyet Yilmaz
AU - Zambon, Alberto
AU - Zambon, Sabina
AU - Zemek, Stanislav
AU - Zenti, Maria G.
AU - Zlatohlavek, Lukas
AU - Zuurbier, Linda
N1 - Publisher Copyright:
© 2024 American Medical Association. All rights reserved.
PY - 2024/4/10
Y1 - 2024/4/10
N2 - IMPORTANCE Homozygous familial hypercholesterolemia (HoFH) is a rare genetic condition characterized by extremely increased low-density lipoprotein (LDL) cholesterol levels and premature atherosclerotic cardiovascular disease (ASCVD). Heterozygous familial hypercholesterolemia (HeFH) is more common than HoFH, and women with HeFH are diagnosed later and undertreated compared to men; it is unknown whether these sex differences also apply to HoFH. OBJECTIVE To investigate sex differences in age at diagnosis, risk factors, lipid-lowering treatment, and ASCVD morbidity and mortality in patients with HoFH. DESIGN, SETTING, AND PARTICIPANTS Sex-specific analyses for this retrospective cohort study were performed using data from the HoFH International Clinical Collaborators (HICC) registry, the largest global dataset of patients with HoFH, spanning 88 institutions across 38 countries. Patients with HoFH who were alive during or after 2010 were eligible for inclusion. Data entry occurred between February 2016 and December 2020. Data were analyzed from June 2022 to June 2023. MAIN OUTCOMES AND MEASURES Comparison betweenwomen and men with HoFH regarding age at diagnosis, presence of risk factors, lipid-lowering treatment, prevalence, and onset and incidence of ASCVD morbidity (myocardial infarction [MI], aortic stenosis, and combined ASCVD outcomes) and mortality. RESULTS Data from 389 women and 362 men with HoFH from 38 countries were included. Women and men had similar age at diagnosis (median [IQR], 13 [6-26] years vs 11 [5-27] years, respectively), untreated LDL cholesterol levels (mean [SD], 579 [203] vs 596 [186]mg/dL, respectively), and cardiovascular risk factor prevalence, except smoking (38 of 266 women [14.3%] vs 59 of 217 men [27.2%], respectively). Prevalence of MI was lower in women (31 of 389 [8.0%]) than men (59 of 362 [16.3%]), but age at first MI was similar (mean [SD], 39 [13] years in women vs 38 [13] years in men). Treated LDL cholesterol levels and lipid-lowering therapy were similar in both sexes, in particular statins (248 of 276 women [89.9%] vs 235 of 258 men [91.1%]) and lipoprotein apheresis (115 of 317 women [36.3%] vs 118 of 304 men [38.8%]). Sixteen years after HoFH diagnosis, women had statistically significant lower cumulative incidence of MI (5.0% in women vs 13.7%in men; subdistribution hazard ratio [SHR], 0.37; 95%CI, 0.21-0.66) and nonsignificantly lower all-cause mortality (3.0% in women vs 4.1% in men; HR, 0.76; 95%CI, 0.40-1.45) and cardiovascular mortality (2.6% in women vs 4.1% in men; SHR, 0.87; 95%CI, 0.44-1.75). CONCLUSIONS AND RELEVANCE In this cohort study of individuals with known HoFH, MI was higher in men compared with women yet age at diagnosis and at first ASCVD event were similar. These findings suggest that early diagnosis and treatment are important in attenuating the excessive cardiovascular risk in both sexes.
AB - IMPORTANCE Homozygous familial hypercholesterolemia (HoFH) is a rare genetic condition characterized by extremely increased low-density lipoprotein (LDL) cholesterol levels and premature atherosclerotic cardiovascular disease (ASCVD). Heterozygous familial hypercholesterolemia (HeFH) is more common than HoFH, and women with HeFH are diagnosed later and undertreated compared to men; it is unknown whether these sex differences also apply to HoFH. OBJECTIVE To investigate sex differences in age at diagnosis, risk factors, lipid-lowering treatment, and ASCVD morbidity and mortality in patients with HoFH. DESIGN, SETTING, AND PARTICIPANTS Sex-specific analyses for this retrospective cohort study were performed using data from the HoFH International Clinical Collaborators (HICC) registry, the largest global dataset of patients with HoFH, spanning 88 institutions across 38 countries. Patients with HoFH who were alive during or after 2010 were eligible for inclusion. Data entry occurred between February 2016 and December 2020. Data were analyzed from June 2022 to June 2023. MAIN OUTCOMES AND MEASURES Comparison betweenwomen and men with HoFH regarding age at diagnosis, presence of risk factors, lipid-lowering treatment, prevalence, and onset and incidence of ASCVD morbidity (myocardial infarction [MI], aortic stenosis, and combined ASCVD outcomes) and mortality. RESULTS Data from 389 women and 362 men with HoFH from 38 countries were included. Women and men had similar age at diagnosis (median [IQR], 13 [6-26] years vs 11 [5-27] years, respectively), untreated LDL cholesterol levels (mean [SD], 579 [203] vs 596 [186]mg/dL, respectively), and cardiovascular risk factor prevalence, except smoking (38 of 266 women [14.3%] vs 59 of 217 men [27.2%], respectively). Prevalence of MI was lower in women (31 of 389 [8.0%]) than men (59 of 362 [16.3%]), but age at first MI was similar (mean [SD], 39 [13] years in women vs 38 [13] years in men). Treated LDL cholesterol levels and lipid-lowering therapy were similar in both sexes, in particular statins (248 of 276 women [89.9%] vs 235 of 258 men [91.1%]) and lipoprotein apheresis (115 of 317 women [36.3%] vs 118 of 304 men [38.8%]). Sixteen years after HoFH diagnosis, women had statistically significant lower cumulative incidence of MI (5.0% in women vs 13.7%in men; subdistribution hazard ratio [SHR], 0.37; 95%CI, 0.21-0.66) and nonsignificantly lower all-cause mortality (3.0% in women vs 4.1% in men; HR, 0.76; 95%CI, 0.40-1.45) and cardiovascular mortality (2.6% in women vs 4.1% in men; SHR, 0.87; 95%CI, 0.44-1.75). CONCLUSIONS AND RELEVANCE In this cohort study of individuals with known HoFH, MI was higher in men compared with women yet age at diagnosis and at first ASCVD event were similar. These findings suggest that early diagnosis and treatment are important in attenuating the excessive cardiovascular risk in both sexes.
UR - http://www.scopus.com/inward/record.url?scp=85185923456&partnerID=8YFLogxK
U2 - 10.1001/jamacardio.2023.5597
DO - 10.1001/jamacardio.2023.5597
M3 - Article
C2 - 38353972
SN - 2380-6583
VL - 9
SP - 313
EP - 322
JO - JAMA Cardiology
JF - JAMA Cardiology
IS - 4
ER -