Chylomicronemia syndrome: Familial or not?

被引:18
|
作者
Warden, Bruce A. [1 ]
Minnier, Jessica [1 ,2 ]
Duell, P. Barton [1 ]
Fazio, Sergio [1 ]
Shapiro, Michael D. [1 ]
机构
[1] Oregon Hlth & Sci Univ, Ctr Prevent Cardiol, Knight Cardiovasc Inst, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, OHSU PSU Sch Publ Hlth, Portland, OR 97201 USA
关键词
Chylomicronemia; Prevalence; Diagnosis; Pharmacotherapy; RECOMMENDATIONS; DIAGNOSIS;
D O I
10.1016/j.jacl.2020.01.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BACKGROUND: Chylomicronemia syndrome (CS) is a metabolic condition characterized by severely elevated plasma triglycerides (>880 mg/dL) and high rates of morbidity and mortality. The syndrome can be classified into two major groups: monogenic familial chylomicronemia syndrome (FCS) and multifactorial chylomicronemia syndrome (MCS), the frequencies of which are ill-defined. OBJECTIVE: The objective of the study was to characterize the prevalence of the most common and rarest subsets of this syndrome, MCS and FCS, respectively, in a single-center, real-world setting. METHODS: This was a retrospective cross-sectional study of patients with plasma triglycerides 880 mg/dL. The criteria used for identification of patients with FCS were modeled after a Food and Drug Administration endorsed set of parameters. Less stringent criteria that removed the requirement for pancreatitis were used to classify MCS. Full criteria are described in detail in the article. RESULTS: Of the 2,342,136 patient records queried, 578 had triglycerides >= 880 mg/dL (0.025%), of which 86 had a documented history of pancreatitis. Five patients who met the criteria for FCS were identified (three genetically confirmed), resulting in an estimated prevalence of similar to 1-2 per 1,000,000. On the other hand, MCS was identified in 186 patients, corresponding to an estimated prevalence of similar to 1 in 12,000. There were 5181 cases of pancreatitis (0.22% of the entire cohort), 86 of which occurred in subjects with triglycerides >= 880 mg/dL (1.7% of cases of pancreatitis). Rates of pancreatitis in this subset were elevated at 6.5%, 100%, and 17.8%, among patients with MCS, FCS, and secondary hypertriglyceridemia, respectively. CONCLUSIONS: CS is an uncommon condition, but it is associated with significant complications, regardless of etiology. Among patients with CS, MCS was 40- to 60-fold more prevalent than FCS and associated with frequent morbidity. Therefore, disease recognition and treatment should extend to all forms of CS pursuant to the clinical presentation. (C) 2020 National Lipid Association. All rights reserved.
引用
收藏
页码:201 / 206
页数:6
相关论文
共 50 条
  • [31] Pregnancy in Familial Chylomicronemia syndrome: Plasmapheresis as Therapeutic Approach
    Dunja, Leskovar
    Marina, Sabic
    Drazen, Perica
    Nediljko, Sucur
    Ana, Godan Hauptman
    Iveta, Mercep
    Fran, Borovecki
    Bojan, Jelakovic
    Zeljko, Reiner
    Ivan, Pecin
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 2021, 116 : 22 - 22
  • [32] FAMILIAL CHYLOMICRONEMIA SYNDROME: DESCRIPTION OF A FRENCH CANADIAN COHORT
    Baass, Alexis
    Paquette, Martine
    Dufour, Robert
    [J]. ATHEROSCLEROSIS SUPPLEMENTS, 2018, 32 : 15 - 15
  • [33] Targeting APOC3 in the Familial Chylomicronemia Syndrome
    Gaudet, Daniel
    Brisson, Diane
    Tremblay, Karine
    Alexander, Veronica J.
    Singleton, Walter
    Hughes, Steven G.
    Geary, Richard S.
    Baker, Brenda F.
    Graham, Mark J.
    Crooke, Rosanne M.
    Witztum, Joseph L.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2014, 371 (23): : 2200 - 2206
  • [34] EFFECTIVENESS AND SAFETY OF LOMITAPIDE IN A PATIENT WITH FAMILIAL CHYLOMICRONEMIA SYNDROME
    Giammanco, A.
    Cefalu, A. B.
    Noto, D.
    Spina, R.
    Cabibi, D.
    Barbagallo, C. M.
    Averna, M.
    [J]. ATHEROSCLEROSIS, 2021, 331 : E181 - E181
  • [35] Editorial commentary: Dietary management of familial chylomicronemia syndrome
    Williams, Lauren
    Wilson, Don P.
    [J]. JOURNAL OF CLINICAL LIPIDOLOGY, 2016, 10 (03) : 462 - 465
  • [36] Effectiveness and safety of lomitapide in a patient with familial chylomicronemia syndrome
    Angelo B. Cefalù
    Antonina Giammanco
    Davide Noto
    Rossella Spina
    Daniela Cabibi
    Carlo M. Barbagallo
    Maurizio Averna
    [J]. Endocrine, 2021, 71 : 344 - 350
  • [37] Roundtable discussion: Familial chylomicronemia syndrome: Diagnosis and management
    Brown, William Virgil
    Goldberg, Ira
    Duell, Barton
    Gaudet, Daniel
    [J]. JOURNAL OF CLINICAL LIPIDOLOGY, 2018, 12 (02) : 254 - 263
  • [38] Prevalence of familial chylomicronemia syndrome in a quaternary care center
    Pallazola, Vincent A.
    Sajja, Aparna
    Derenbecker, Robert
    Ogunmoroti, Oluseye
    Park, Jihwan
    Sathiyakumar, Vasanth
    Martin, Seth S.
    [J]. EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY, 2020, 27 (19) : 2276 - 2278
  • [39] DIAGNOSIS AND MANAGEMENT OF FAMILIAL CHYLOMICRONEMIA SYNDROME IN A NEWBORN GIRL
    Lanza, M.
    Fasciana, Teresa Maria Grazia
    Scalzo, A.
    Scrimali, C.
    Savarino, G.
    Brucato, Federica
    Insinga, V.
    Bonacasa, C.
    Giammanco, Antonina
    Barbagallo, C. M.
    Carta, M.
    Noto, D.
    Cefalu, A. B.
    Giuffre, M.
    Averna, M. R.
    [J]. ATHEROSCLEROSIS, 2024, 395
  • [40] Familial Chylomicronemia Syndrome (FCS): Recent Data on Diagnosis and Treatment
    Gallo, Antonio
    Beliard, Sophie
    D'Erasmo, Laura
    Bruckert, Eric
    [J]. CURRENT ATHEROSCLEROSIS REPORTS, 2020, 22 (11)