Positive renal familial history in IgA nephropathy is associated with worse renal outcomes: a single-center longitudinal study

被引:6
作者
Sato, Yoshinori [1 ]
Tsukaguchi, Hiroyasu [2 ]
Higasa, Koichiro [3 ]
Kawata, Naoto [1 ]
Inui, Kiyoko [1 ]
Tran Nguyen Truc Linh [2 ]
Tran Thuy Huong Quynh [2 ]
Yoshihiko, Inoue [1 ]
Koiwa, Fumihiko [1 ]
Yoshimura, Ashio [1 ,4 ]
机构
[1] Showa Univ, Fujigaoka Hosp, Sch Med, Dept Internal Med,Div Nephrol,Aoba Ku, 1-30 Fujigaoka, Yokohama, Kanagawa 2278501, Japan
[2] Kansai Med Univ, Dept Internal Med 2, Hirakata, Osaka 5731010, Japan
[3] Kansai Med Univ, Inst Biomed Sci, Dept Genome Anal, Hirakata, Osaka 5731010, Japan
[4] Shinyokohama Daiichi Clin, Yokohama, Kanagawa, Japan
关键词
IgA nephropathy; End-stage renal disease; Familial history; Genetic factor; Proteinuria; INCREASED RISK; VARIANTS; GENETICS; THERAPY; DISEASE;
D O I
10.1186/s12882-021-02425-8
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
BackgroundIgA nephropathy (IgAN) is the most common primary glomerulonephritis worldwide. Although most IgAN cases are sporadic, few show a familial aggregation. However, the prevalence and prognosis of IgAN individuals with positive familial history (FH) of renal disorders remains uncertain. To address these issues, we conducted a longitudinal observational study on a single-institution cohort of patients with biopsy-proven IgAN.MethodsA total of 467 IgAN patients who underwent renal biopsy during 1994 to 2019 were ascertained to have positive- or negative-FH by history taking and were followed for an average of 8.9years. We compared the clinical and pathological features of the two subgroups. The primary outcome, a composite of a hard endpoint (end-stage renal disease [ESRD]) and surrogate endpoint (a 50% or more reduction in the estimated glomerular filtration rate [eGFR] from baseline), was evaluated. To estimate the risk for progression to ESRD, a Cox proportional hazards analysis was performed for a subset of patients who underwent follow-up for >2years and had an eGFR >30mL/min/1.73m(2) at baseline (n=389; observation, 8.7years).ResultsPositive-FH subtype accounted for 11.6% (n =54) of all IgAN patients. At baseline, there were no significant differences between the positive- and negative-FH subgroups regarding age, sex, comorbid disease, MEST-C score, observation period, and therapeutic interventions. However, the eGFR value at baselines was significantly lower in the positive-FH subgroup than in the negative-FH subgroup (P <0.01). On multivariate analysis, positive-FH emerged an independent determinant of poorer renal outcomes (odds ratio, 2.31; 95% confidence interval, 1.10-4.85; P =0.03), after adjusting for confounding factors. eGFR at follow-up was significantly lower in the positive-FH subgroup than in the negative-FH subgroup after adjustment for age and observation period.ConclusionsPositive-FH was found in 11.6% of all IgAN patients, consistent with the incidence seen in previous literature. A significantly lower eGFR at baseline and last follow-up and unfavorable renal outcomes in the positive-FH subgroup suggest that certain genetic risk factors predisposing to renal failure may exist in a fraction of our IgAN cohort. (331 words).
引用
收藏
页数:10
相关论文
共 22 条
  • [11] The genetics and immunobiology of IgA nephropathy
    Kiryluk, Krzysztof
    Novak, Jan
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2014, 124 (06) : 2325 - 2332
  • [12] Type IV Collagen Mutations in Familial IgA Nephropathy
    Li, Yif
    Groopman, Emily E.
    D'Agati, Vivette
    Prakash, Sindhuri
    Zhang, Junying
    Mizerska-Wasiak, Malgorzata
    Caliskan, Yasar
    Fasel, David
    Karnib, Hussein H.
    Bono, Luisa
    Al Omran, Sadek
    Al Sabban, Essam
    Kiryluk, Krzysztof
    Caridi, Gianluca
    Ghiggeri, Gian Marco
    Sanna-Cherchi, Simone
    Scolari, Francesco
    Gharavi, Ali G.
    [J]. KIDNEY INTERNATIONAL REPORTS, 2020, 5 (07): : 1075 - 1078
  • [13] New developments in the genetics, pathogenesis, and therapy of IgA nephropathy
    Magistroni, Riccardo
    D'Agati, Vivette D.
    Appel, Gerald B.
    Kiryluk, Krzysztof
    [J]. KIDNEY INTERNATIONAL, 2015, 88 (05) : 974 - 989
  • [14] Revised Equations for Estimated GFR From Serum Creatinine in Japan
    Matsuo, Seiichi
    Imai, Enyu
    Horio, Masaru
    Yasuda, Yoshinari
    Tomita, Kimio
    Nitta, Kosaku
    Yamagata, Kunihiro
    Tomino, Yasuhiko
    Yokoyama, Hitoshi
    Hishida, Akira
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2009, 53 (06) : 982 - 992
  • [15] Prognosis in IgA Nephropathy: 30-Year Analysis of 1,012 Patients at a Single Center in Japan
    Moriyama, Takahito
    Tanaka, Kayu
    Iwasaki, Chihiro
    Oshima, Yasuko
    Ochi, Ayami
    Kataoka, Hiroshi
    Itabashi, Mitsuyo
    Takei, Takashi
    Uchida, Keiko
    Nitta, Kosaku
    [J]. PLOS ONE, 2014, 9 (03):
  • [16] Schena FP, 2002, J AM SOC NEPHROL, V13, P453, DOI 10.1681/ASN.V132453
  • [17] Increased Lifetime Risk of ESRD in Familial IgA Nephropathy
    Shi, Manman
    Yu, Shuwen
    Ouyang, Yan
    Jin, Yuanmeng
    Chen, Zijin
    Wei, Wenjie
    Fang, Zhengying
    Du, Wen
    Wang, Zhaohui
    Weng, Qinjie
    Tong, Jun
    Pan, Xiaoxia
    Wang, Weiming
    Krzysztof, Kiryluk
    Chen, Nan
    Xie, Jingyuan
    [J]. KIDNEY INTERNATIONAL REPORTS, 2021, 6 (01): : 91 - 100
  • [18] An Exome Sequencing Study of 10 Families with IgA Nephropathy
    Stapleton, Caragh P.
    Kennedy, Claire
    Fennelly, Neil K.
    Murray, Susan L.
    Connaughton, Dervla M.
    Dorman, Anthony M.
    Doyle, Brendan
    Cavalleri, Gianpiero L.
    Conlon, Peter J.
    [J]. NEPHRON, 2020, 144 (02) : 72 - 83
  • [19] Oxford Classification of IgA nephropathy 2016: an update from the IgA Nephropathy Classification Working Group
    Trimarchi, Hernan
    Barratt, Jonathan
    Cattran, Daniel C.
    Cook, H. Terence
    Coppo, Rosanna
    Haas, Mark
    Liu, Zhi-Hong
    Roberts, Ian S. D.
    Yuzawa, Yukio
    Zhang, Hong
    Feehally, John
    [J]. KIDNEY INTERNATIONAL, 2017, 91 (05) : 1014 - 1021
  • [20] Assessment of kidney function in children by enzymatic determination of 2-or 24-h creatinine clearance: comparison with inulin clearance
    Uemura, Osamu
    Nagai, Takuhito
    Yamakawa, Satoshi
    Kaneko, Tetsuji
    Hibi, Yoshiko
    Yamasaki, Yasuhito
    Yamamoto, Masaki
    Nakano, Masaru
    Iwata, Naoyuki
    Hibino, Satoshi
    [J]. CLINICAL AND EXPERIMENTAL NEPHROLOGY, 2016, 20 (03) : 462 - 468