Novel metabolic phenotypes for extrahepatic complication of nonalcoholic fatty liver disease

被引:10
作者
Yi, Jiayi [1 ]
Wang, Lili [1 ]
Guo, Jiajun [3 ]
Ren, Xiangpeng [2 ,4 ]
机构
[1] Jiaxing Univ, Med Coll, Dept Biochem, Jiaxing, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Fuwai Hosp, Natl Ctr Cardiovasc Dis, Dept Cardiol, Beijing, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Cardiol, Chengdu, Sichuan, Peoples R China
[4] Jiaxing Univ, Med Coll, Dept Biochem, 899 Guangqiong Rd, Jiaxing 314001, Zhejiang, Peoples R China
关键词
CARDIOVASCULAR-DISEASE; CLUSTER-ANALYSIS; STEATOHEPATITIS; FIBROSIS; PROGRESSION; NAFLD;
D O I
10.1097/HC9.0000000000000016
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims:Phenotypic heterogeneity among patients with NAFLD is poorly understood. We aim to identify clinically important phenotypes within NAFLD patients and assess the long-term outcomes among different phenotypes. Methods:We analyzed the clinical data of 2311 participants from the Third National Health and Nutrition Examination Survey (NHANES III) and their linked mortality data through December 2019. NAFLD was diagnosed by ultrasonographic evidence of hepatic steatosis without other liver diseases and excess alcohol use. A 2-stage cluster analysis was applied to identify clinical phenotypes. We used Cox proportional hazard models to explore all-cause and cause-specific mortality between clusters. Results:We identified 3 NAFLD phenotypes. Cluster 1 was characterized by young female patients with better metabolic profiles and lower prevalence of comorbidities; Cluster 2 by obese females with significant insulin resistance, diabetes, inflammation, and advanced fibrosis and Cluster 3 by male patients with hypertension, atherogenic dyslipidemia, and liver and kidney damage. In a median follow-up of 26 years, 989 (42.8%) all-cause mortality occurred. Cluster 1 patients presented the best prognosis, whereas Cluster 2 and 3 had higher risks of all-cause (Cluster 2-adjusted HR: 1.48, 95% CI: 1.16-1.90; Cluster 3-adjusted HR: 1.29, 95% CI: 1.01-1.64) and cardiovascular (Cluster 2-adjusted HR: 2.01, 95% CI: 1.18-3.44; Cluster 3-adjusted HR: 1.75, 95% CI: 1.03-2.97) mortality. Conclusions:Three phenotypically distinct and clinically meaningful NAFLD subgroups have been identified with different characteristics of metabolic profiles. This study reveals the substantial disease heterogeneity that exists among NAFLD patients and underscores the need for granular assessments to define phenotypes and improve clinical practice.
引用
收藏
页数:10
相关论文
共 40 条
  • [1] Non-alcoholic fatty liver disease and its relationship with cardiovascular disease and other extrahepatic diseases
    Adams, Leon A.
    Anstee, Quentin M.
    Tilg, Herbert
    Targher, Giovanni
    [J]. GUT, 2017, 66 (06) : 1138 - 1153
  • [2] The NAFLD fibrosis score: A noninvasive system that identifies liver fibrosis in patients with NAFLD
    Angulo, Paul
    Hui, Jason M.
    Marchesini, Giulio
    Bugianesi, Ellisabetta
    George, Jacob
    Farrell, Geoffrey C.
    Enders, Felicity
    Saksena, Sushma
    Burt, Alastair D.
    Bida, John P.
    Lindor, Keith
    Sanderson, Schuyler O.
    Lenzi, Marco
    Adams, Leon A.
    Kench, James
    Therneau, Terry M.
    Day, Christopher P.
    [J]. HEPATOLOGY, 2007, 45 (04) : 846 - 854
  • [3] Clinical implications of idiopathic pulmonary arterial hypertension phenotypes defined by cluster analysis
    Badagliacca, Roberto
    Rischard, Franz
    Papa, Silvia
    Kubba, Saad
    Vanderpool, Rebecca
    Yuan, Jason X-J
    Garcia, Joe G. N.
    Airhart, Sophia
    Poscia, Roberto
    Pezzuto, Beatrice
    Manzi, Giovanna
    Miotti, Cristiano
    Luongo, Federico
    Scoccia, Gianmarco
    Sciomer, Susanna
    Torre, Roberto
    Fedele, Francesco
    Vizza, Carmine Dario
    [J]. JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2020, 39 (04) : 310 - 320
  • [4] Nonalcoholic fatty liver disease
    Brunt, Elizabeth M.
    Wong, Vincent W. -S.
    Nobili, Valerio
    Day, Christopher P.
    Sookoian, Silvia
    Maher, Jacquelyn J.
    Bugianesi, Elisabetta
    Sirlin, Claude B.
    Neuschwander-Tetri, BrentA.
    Rinella, Mary E.
    [J]. NATURE REVIEWS DISEASE PRIMERS, 2015, 1
  • [5] Charrad M, 2014, J STAT SOFTW, V61, P1
  • [6] A new definition for metabolic dysfunction-associated fatty liver disease: An international expert consensus statement
    Eslam, Mohammed
    Newsome, Philip N.
    Sarin, Shiv K.
    Anstee, Quentin M.
    Targher, Giovanni
    Romero-Gomez, Manuel
    Zelber-Sagi, Shira
    Wong, Vincent Wai-Sun
    Dufour, Jean-Francois
    Schattenberg, Joern M.
    Kawaguchi, Takumi
    Arrese, Marco
    Valenti, Luca
    Shiha, Gamal
    Tiribelli, Claudio
    Yki-Jarvinen, Hannele
    Fan, Jian-Gao
    Gronbaek, Henning
    Yilmaz, Yusuf
    Cortez-Pinto, Helena
    Oliveira, Claudia P.
    Bedossa, Pierre
    Adams, Leon A.
    Zheng, Ming-Hua
    Fouad, Yasser
    Chan, Wah-Kheong
    Mendez-Sanchez, Nahum
    Ahn, Sang Hoon
    Castera, Laurent
    Bugianesi, Elisabetta
    Ratziu, Vlad
    George, Jacob
    [J]. JOURNAL OF HEPATOLOGY, 2020, 73 (01) : 202 - 209
  • [7] Modeling the epidemic of nonalcoholic fatty liver disease demonstrates an exponential increase in burden of disease
    Estes, Chris
    Razavi, Homie
    Loomba, Rohit
    Younossi, Zobair
    Sanyal, Arun J.
    [J]. HEPATOLOGY, 2018, 67 (01) : 123 - 133
  • [8] Non-alcoholic fatty liver disease and cardiovascular risk: Pathophysiological mechanisms and implications
    Francque, Sven M.
    van der Graaff, Denise
    Kwanten, Wilhelmus J.
    [J]. JOURNAL OF HEPATOLOGY, 2016, 65 (02) : 425 - 443
  • [9] Phenotyping chronic pulmonary aspergillosis by cluster analysis
    Godet, Cendrine
    Laurent, Francois
    Beraud, Guillaume
    Toper, Cecile
    Camara, Boubou
    Philippe, Bruno
    Germaud, Patrick
    Cottin, Vincent
    Beigelman-Aubry, Catherine
    Khalil, Antoine
    Blouin, Pascal
    Pouriel, Mathilde
    Roblot, France
    Bergeron, Anne
    Cadranel, Jacques
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2015, 46 (05) : 1509 - 1512
  • [10] Hoeper MM., 2022, LANCET RESP MED, V76, P1423