1.Mutation analysis of microRNA-7 gene in Chinese patients with Parkinson's disease.
Xuewei ZHANG ; Jifeng GUO ; Sanxi AI ; Yaceng HU ; Qiying SUN ; Qian XU ; Zhanyun LU ; Kai LI ; Xiaoli DONG ; Lu SHEN ; Hong JIANG ; Qian PAN ; Kun XIA ; Xinxiang YAN ; Beisha TANG
Journal of Central South University(Medical Sciences) 2012;37(12):1189-1192
OBJECTIVE:
To investigate the mutation of small sequence changes in microRNA-7 gene in Chinese patients with Parkinson's disease (PD).
METHODS:
We analyzed miR-7 variants in 225 PD patients from Chinese Han group by DNA sequence.
RESULTS:
None of the patients had miR-7 variants.
CONCLUSION
MiR-7 variation is not associated with PD in Chinese patients.
Aged
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Base Sequence
;
China
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ethnology
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Female
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Humans
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Male
;
MicroRNAs
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genetics
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Middle Aged
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Molecular Sequence Data
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Mutation
;
Parkinson Disease
;
genetics
2.Low-dose rituximab improves progression in early-stage medium-to-high-risk membranous nephropathy:an exploratory study
Qiuyu XU ; Sanxi AI ; Gangan WANG ; Chunyu JIA ; Jiahui WANG ; Ke ZHENG ; Yan QIN ; Gang CHEN ; Xuemei LI
Chinese Journal of Clinical Pharmacology and Therapeutics 2024;29(7):744-751
Membranous nephropathy(MN)is the predominant cause of primary nephrotic syn-drome(NS)among adults.The identification of PLA2R as target antigen has brought about a pro-found transformation in the management of MN,offering a basis for the utilization of B-cell deplet-ing agents such as rituximab(RTX).The question of whether early intervention targeting antibodies can effectively impede the progression of MN,contrib-uting to enhanced disease control and long-term renal outcomes for patients,remains further explo-ration.We analyzed demographic data,laboratory parameters,and renal involvement in 13 patients with PLA2R antibody-related MN who received at least one RTX treatment at our center from Octo-ber 2019 to March 2023.Early-stage medium-to-high-risk MN was defined as baseline or admission anti-PLA2R antibody levels exceeding 50 RU/mL,ex-cluding patients who already presented with ne-phrotic syndrome at baseline.The median duration of MN at the initiation of the first RTX treatment was 4.1 months(IQR 1-7.7),and the median follow-up time after RTX therapy was 27 months(IQR 23-45).All patients had commenced renin-angiotensin system inhibitors before receiving RTX.Following RTX therapy,none of the 13 patients progressed to NS during the follow-up period,and 12 patients achieved complete or partial remission at the 2-year follow-up or the last visit.No deaths,severe infections,or other serious adverse reactions oc-curred during the follow-up period.In conclusion,RTX demonstrates favorable efficacy and safety in early-stage,medium-to-high-risk MN patients.Initi-ating antibody clearance therapy in these patients may be beneficial for long-term disease control and distant renal outcomes.