Sex Differences in Diagnosis, Treatment, and Cardiovascular Outcomes in Homozygous Familial Hypercholesterolemia

Author:

Mulder Janneke W. C. M.1,Tromp Tycho R.2,Al-Khnifsawi Mutaz3,Blom Dirk J.4,Chlebus Krysztof56,Cuchel Marina7,D’Erasmo Laura8,Gallo Antonio9,Hovingh G. Kees2,Kim Ngoc Thanh1011,Long Jiang12,Raal Frederick J.13,Schonck Willemijn A. M.2,Soran Handrean14,Truong Thanh-Huong1516,Boersma Eric17,Roeters van Lennep Jeanine E.1, ,Alareedh Mohammed D.18,Alieva Rano18,Allevi Massimiliano18,Altunkeser Bulent B.18,Al-Waili Khalid18,Al-Zamili Ali F.18,Arca Marcello18,Atzori Luigi18,Averna Maurizio18,Ayesh Mahmoud H.18,Azar Sami T.18,Banderali Giuseppe18,Baratta Francesco18,Bartuli Andrea18,Béliard Sophie18,Bianconi Vanessa18,Bini Simone18,Bin Thani Khalid18,Bitar Fadi F.18,Blaha Vladimir18,Bonomo Katia18,Bourbon Mafalda18,Branchi Adriana18,Brothers Julie A.18,Bruckert Eric18,Brunham Liam R.18,Bruzzi Patrizia18,Bucci Marco18,Buonuomo Paola S.18,Calabrò Paolo18,Calandra Sebastiano18,Carubbi Francesca18,Cassiman David18,Casula Manuela18,Catapano Alberico L.18,Cavalot Franco18,Cefalù Angelo B.18,Cesaro Arturo18,Ceska Richard18,Charng Min-Ji18,Cipollone Francesco18,Cohen Hofit18,D'Addato Sergio18,Dal Pino Beatrice18,Dann Eldad J.18,Defesche Joep C.18,Del Ben Maria18,Demircioglu Sinan18,Descamps Olivier S.18,Di Costanzo Alessia18,Di Taranto Maria D.18,Do Doan-Loi18,Durst Ronen18,Dvorakova Jana18,Ebenbichler Christoph F.18,Elis Avishay18,Emil Sameh18,Ezhov Marat V.18,Fahed Akl C.18,Fasano Tommaso18,Ferri Claudio18,Fogacci Federica18,Formisano Elena18,Fortunato Giuliana18,Francis Gordon A.18,Freiberger Tomas18,Galimberti Federica18,Gaspar Isabel M.18,Genest Jacques18,Gentile Marco18,Giammanco Antonina18,Gokce Cumali18,Greber-Platzer Susanne18,Grigore Liliana18,Groselj Urh18,Harada-Shiba Mariko18,Hartgers Merel L.18,Hegele Robert A.18,Horak Pavel18,Hori Mika18,Hudgins Lisa C.18,Hussein Osama18,Iannuzzo Gabriella18,Ilhan Osman18,Iughetti Lorenzo18,Kayikcioglu Meral18,Kaynar Leyla G.18,Kennedy Brooke A.18,Khovidhunkit Weerapan18,Kolovou Genovefa18,Kose Melis18,Kuku Irfan18,Kurtoglu Erdal18,Lalic Katarina S.18,Le Hong-An18,Le Thanh-Tung18,Leitersdorf Eran18,Liberopoulos Evangelos18,Lyons Alexander R.M.18,Madriz Ramón18,Mandraffino Giuseppe18,Mäser Martin18,Mehta Roopa18,Mitchenko Olena18,Mombelli Giuliana18,Montalcini Tiziana18,Morace Carmela18,Moubarak Elie M.18,Muntoni Sandro18,Naguib Tarek A.18,Nascimbeni Fabio18,Nawawi Hapizah18,Nemer Georges18,Nguyen Mai-Ngoc T.18,Notargiacomo Serena18,Okutan Harika18,Ozcebe Osman I.18,Pang Jing18,Passaro Angelina18,Pavanello Chiara18,Pecchioli Lorenzo18,Pecchioli Valerio18,Pederiva Cristina18,Pekkolay Zafer18,Pellegatta Fabio18,Piro Salvatore18,Pirro Matteo18,Pisciotta Livia18,Pujia Arturo18,Ray Kausik K.18,Reda Ashraf18,Reijman M. Doortje18,Reiner Željko18,Rhadi Sabah H.18,Rizzi Luigi18,Romandini Alessandra18,Ruel Isabelle18,Rymen Daisy18,Sadiq Fouzia18,Sag Saim18,Salcioglu Osman Z.18,Santos Raul D.18,Sanz Juana M.18,Sarzani Riccardo18,Sbrana Francesco18,Schurr Daniel18,Scicali Roberto18,Setia Nitika18,Shaghee Foaad K.18,Shek Aleksandr18,Sherman Mark H.18,Soska Vladimir18,Stevens Christophe A.T.18,Stroes Erik S.G.18,Stulnig Thomas M.18,Suppressa Patrizia18,Susekov Andrey V.18,Tarugi Patrizia18,Temizhan Ahmet18,Tichy Lukas18,Trenti Chiara18,Tromp Tycho R.18,Urbanek Robin18,Vallejo-Vaz Antonio J.18,Vaverkova helena18,Verma Ishwar C.18,Vrablik Michal18,Wang Luya18,Watts Gerald F.18,Werba José P.18,Wiegman Albert18,Witters Peter18,Yenercag Mustafa18,Yilmaz Mehmet18,Yilmaz Yasar Hamiyet18,Zambon Alberto18,Zambon Sabina18,Zemek Stanislav18,Zenti Maria G.18,Zlatohlavek Lukas18,Zuurbier Linda18

Affiliation:

1. Department of Internal Medicine, Erasmus Medical Center Cardiovascular Institute, University Medical Center Rotterdam, Rotterdam, the Netherlands

2. Department of Vascular Medicine, Amsterdam University Medical Centers, Academic Medical Center, Amsterdam, the Netherlands

3. University of Al-Qadisiyah, College of Pharmacy, Diwaniya City, Iraq

4. Department of Medicine, Division of Lipidology and Cape Heart Institute, University of Cape Town, Cape Town, South Africa

5. 1st Department of Cardiology, Medical University of Gdańsk, Gdańsk, Poland

6. National Centre of Familial Hypercholesterolaemia, Gdańsk, Poland

7. Department of Medicine, Division of Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia

8. Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy

9. Lipidology and Cardiovascular Prevention Unit, Department of Nutrition, Sorbonne Université, Institut national de la santé et de la recherche médicale UMR 1166, Assistance Publique–Hôpitaux de Paris, Hôpital Pitié-Salpètriêre, Paris, France

10. Vietnam National Heart Institute, Bach Mai Hospital, Hanoi, Vietnam

11. Department of Cardiology, Hanoi Medical University, Hanoi, Vietnam

12. Department of Atherosclerosis, Beijing Anzhen Hospital, Capital Medical University, The Key Laboratory of Remodeling–Related Cardiovascular Diseases, Ministry of Education, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing, China

13. Carbohydrate and Lipid Metabolism Research Unit, Faculty of Health Sciences, University of Witwatersrand, Johannesburg, South Africa

14. Department of Diabetes, Endocrinology and Metabolism and Manchester National Institute of Health Research/Wellcome Trust Clinical Research Facility, Manchester University NHS Foundation Trust, Manchester, United Kingdom

15. Faculty of Medicine, Phenikaa University, Hanoi City, Vietnam

16. Vietnam Atherosclerosis Society, Hanoi, Vietnam

17. Department of Cardiology, Erasmus Medical Center Cardiovascular Institute, University Medical Center Rotterdam, Rotterdam, the Netherlands

18. for the Homozygous Familial Hypercholesterolemia International Clinical Collaborators

Abstract

ImportanceHomozygous 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.ObjectiveTo investigate sex differences in age at diagnosis, risk factors, lipid-lowering treatment, and ASCVD morbidity and mortality in patients with HoFH.Design, Setting, and ParticipantsSex-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 MeasuresComparison between women 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.ResultsData 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 RelevanceIn 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.

Publisher

American Medical Association (AMA)

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