Gender differences in hereditary hemorrhagic telangiectasia severity

被引:20
作者
Mora-Lujan, J. M. [1 ,2 ,3 ]
Iriarte, A. [1 ,2 ,3 ]
Alba, E. [1 ,3 ,4 ]
Sanchez-Corral, M. A. [1 ,3 ,5 ]
Cerda, P. [1 ,2 ,3 ]
Cruellas, F. [1 ,3 ,6 ]
Ordi, Q. [1 ,3 ,4 ]
Corbella, X. [1 ,2 ,3 ,7 ]
Ribas, J. [1 ,3 ,8 ]
Castellote, J. [1 ,3 ,9 ]
Riera-Mestre, A. [1 ,2 ,3 ,10 ]
机构
[1] Hosp Univ Bellvitge, HHT Unit, C Feixa Llarga S-N, Barcelona 08907, Spain
[2] Hosp Univ Bellvitge, Internal Med Dept, Barcelona, Spain
[3] Bellvitge Biomed Res Inst IDIBELL, Barcelona, Spain
[4] Hosp Univ Bellvitge, Radiol Dept, Barcelona, Spain
[5] Hosp Univ Bellvitge, Cardiol Dept, Barcelona, Spain
[6] Hosp Univ Bellvitge, Otorhinolaryngol Dept, Barcelona, Spain
[7] Univ Int Catalunya, Fac Med & Hlth Sci, Barcelona, Spain
[8] Hosp Univ Bellvitge, Pneumol Dept, Barcelona, Spain
[9] Hosp Univ Bellvitge, Dept Digest Dis, Liver Transplant Unit, Barcelona, Spain
[10] Univ Barcelona, Fac Med & Hlth Sci, Barcelona, Spain
关键词
Hereditary hemorrhagic telangiectasia; Gender; Arteriovenous malformations; Rare diseases; PULMONARY ARTERIOVENOUS-MALFORMATIONS; LIVER-TRANSPLANTATION; ESTROGEN; MANIFESTATIONS; POPULATION; PREVALENCE; MUTATIONS; EPISTAXIS; ABSCESS; SCORE;
D O I
10.1186/s13023-020-1337-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Gender differences in organ involvement and clinical severity have been poorly described in hereditary hemorrhagic telangiectasia (HHT). The aim of this study was to describe differences in the severity of HHT manifestations according to gender. Methods Severity was measured according to Epistaxis Severity Score (ESS), Simple Clinical Scoring Index for hepatic involvement, a general HHT-score, needing for invasive treatment (pulmonary or brain arteriovenous malformations -AVMs- embolization, liver transplantation or Young's surgery) or the presence of adverse outcomes (severe anemia, emergency department -ED- or hospital admissions and mortality). Results One hundred forty-two (58.7%) women and 100 (41.3%) men were included with a mean age of 48.9 +/- 16.6 and 49 +/- 16.5 years, respectively. Women presented hepatic manifestations (7.1% vs 0%) and hepatic involvement (59.8% vs 47%), hepatic AVMs (28.2% vs 13%) and bile duct dilatation (4.9% vs 0%) at abdominal CT, and pulmonary AVMs at thoracic CT (35.2% vs 23%) more often than men. The Simple Clinical Scoring Index was higher in women (3.38 +/- 1.2 vs 2.03 +/- 1.2), and more men were considered at low risk of harboring clinically significant liver disease than women (61% vs 25.3%). These differences were mantained when considering HHT1 and HHT2 patients separetely. Duodenal telangiectasia were more frequent in men than women (21% vs 9.8%). Invasive treatments were more frequently needed in women (28.2% vs 16%) but men needed attention at the ED more often than women (48% vs 28.2%), with no differences in ESS, HHT-score, anemia hospital admissions or mortality. Conclusions HHT women showed more severe hepatic involvement than men, also among HHT1 and HHT2 patients. Women had higher prevalence of pulmonary AVMs and needed invasive procedures more frequently, while men needed attention at the ED more often. These data might help physicians to individualize HHT patients follow-up.
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页数:10
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共 49 条
  • [1] Systemic bevacizumab for high-output cardiac failure in hereditary hemorrhagic telangiectasia: an international survey of HHT centers
    Al-Samkari, Hanny
    Albitar, Hasan A.
    Olitsky, Scott E.
    Clancy, Marianne S.
    Iyer, Vivek N.
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2019, 14 (01)
  • [2] ALK1 Loss Results in Vascular Hyperplasia in Mice and Humans Through PI3K Activation
    Alsina-Sanchis, Elisenda
    Garcia-Ibanez, Yaiza
    Figueiredo, Ana M.
    Riera-Domingo, Carla
    Figueras, Agnes
    Matias-Guiu, Xavier
    Casanovas, Oriol
    Botella, Luisa M.
    Pujana, Miquel A.
    Riera-Mestre, Antoni
    Graupera, Mariona
    Vinals, Francesc
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2018, 38 (05) : 1216 - 1229
  • [3] 2-DIMENSIONAL CONTRAST ECHOCARDIOGRAPHY IN THE DETECTION AND FOLLOW-UP OF CONGENITAL PULMONARY ARTERIOVENOUS-MALFORMATIONS
    BARZILAI, B
    WAGGONER, AD
    SPESSERT, C
    PICUS, D
    GOODENBERGER, D
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 1991, 68 (15) : 1507 - 1510
  • [4] Genotype-phenotype correlation in hereditary hemorrhagic telangiectasia: Mutations and manifestations
    Bayrak-Toydemir, P
    McDonald, J
    Markewitz, B
    Lewin, S
    Miller, F
    Chou, LS
    Gedge, F
    Tang, W
    Coon, H
    Mao, R
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (05) : 463 - 470
  • [5] ULTRASTRUCTURE AND 3-DIMENSIONAL ORGANIZATION OF THE TELANGIECTASES OF HEREDITARY HEMORRHAGIC TELANGIECTASIA
    BRAVERMAN, IM
    KEH, A
    JACOBSON, BS
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1990, 95 (04) : 422 - 427
  • [6] Neurovascular Manifestations of Hereditary Hemorrhagic Telangiectasia: A Consecutive Series of 376 Patients during 15 Years
    Brinjikji, W.
    Iyer, V. N.
    Yamaki, V.
    Lanzino, G.
    Cloft, H. J.
    Thielen, K. R.
    Swanson, K. L.
    Wood, C. P.
    [J]. AMERICAN JOURNAL OF NEURORADIOLOGY, 2016, 37 (08) : 1479 - 1486
  • [7] The UK prevalence of hereditary haemorrhagic telangiectasia and its association with sex, socioeconomic status and region of residence: a population-based study
    Donaldson, J. W.
    McKeever, T. M.
    Hall, I. P.
    Hubbard, R. B.
    Fogarty, A. W.
    [J]. THORAX, 2014, 69 (02) : 161 - 167
  • [8] Recurrence of Hereditary Hemorrhagic Telangiectasia After Liver Transplantation: Clinical Implications and Physiopathological Insights
    Dumortier, Jerome
    Dupuis-Girod, Sophie
    Valette, Pierre-Jean
    Valent, Alexander
    Guillaud, Olivier
    Saurin, Jean-Christophe
    Hervieu, Valerie
    Robinson, Philip
    Plauchu, Henri
    Paliard, Pierre
    Boillot, Olivier
    Scoazec, Jean-Yves
    [J]. HEPATOLOGY, 2019, 69 (05) : 2232 - 2240
  • [9] Lack of significant estrogen and progesterone receptor expression in nasal telangiectasias in hereditary hemorrhagic telangiectasia: An immunohistochemical analysis
    Eivazi, Behfar
    Werner, Jochen A.
    Roessler, Marion
    Negm, Hesham
    Teymoortash, Afshin
    [J]. ACTA OTO-LARYNGOLOGICA, 2012, 132 (01) : 86 - 89
  • [10] Pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia: Correlations between computed tomography findings and cerebral complications
    Etievant, Johan
    Si-Mohamed, Salim
    Vinurel, Nicolas
    Dupuis-Girod, Sophie
    Decullier, Evelyne
    Gamondes, Delphine
    Khouatra, Chahera
    Cottin, Vincent
    Revel, Didier
    [J]. EUROPEAN RADIOLOGY, 2018, 28 (03) : 1338 - 1344