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).
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页数:10
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