Serum Biomarkers for Early Diagnosis of Chinese X-CGD Children: Case Reports and a Literature Review

Ling Hou , Wan-ting Niu , Hong-yan Ji , Xiu-fen Hu , Feng Fang , Yan-qin Ying

Current Medical Science ›› 2019, Vol. 39 ›› Issue (2) : 343 -348.

PDF
Current Medical Science ›› 2019, Vol. 39 ›› Issue (2) : 343 -348. DOI: 10.1007/s11596-019-2041-3
Article

Serum Biomarkers for Early Diagnosis of Chinese X-CGD Children: Case Reports and a Literature Review

Author information +
History +
PDF

Abstract

Since X-linked chronic granulomatosis disease (X-CGD) exhibits no specific clinical symptoms at an early stage, early diagnosis is difficult and depends predominantly on neonatal screening. Therefore, the aim of this study was to explore routine biomarkers for X-CGD in children and provide clues for early diagnosis. The cases of 10 children with X-CGD diagnosed at Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology from 2013 to 2016 and 122 Chinese children with X-CGD reported in the literature were summarized. Serum biomarkers and clinical symptoms at acute infection were organized. A total of 132 children with X-CGD were enrolled in this study. For 55.8% of the patients, the diagnosis was delayed more than one year after the onset of the first symptoms because no typical clinical symptoms manifested. Children with X-CGD at an acute infection stage showed three recurrent signs in terms of serum biomarkers: (1) the total number of white blood cells (especially N%) was increased significantly, accompanied by anemia in some cases; (2) C-reactive protein (CRP) levels were increased significantly; and (3) most of the patients exhibited very high serum IgG levels (>12 g/L). Diagnosis of X-CGD at an early age is difficult because of its nonspecific clinical features. Our study suggested children with X-CGD suffering acute infection show increases in three typical serum biomarkers, which can provide clues for early diagnosis.

Keywords

children / clinical features / early diagnosis / serum biomarkers / X-linked chronic granulomatosis disease

Cite this article

Download citation ▾
Ling Hou, Wan-ting Niu, Hong-yan Ji, Xiu-fen Hu, Feng Fang, Yan-qin Ying. Serum Biomarkers for Early Diagnosis of Chinese X-CGD Children: Case Reports and a Literature Review. Current Medical Science, 2019, 39(2): 343-348 DOI:10.1007/s11596-019-2041-3

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

HollandSM. Chronic granulomatous disease. Hematol Oncol Clin North Am, 2013, 27(1): 89-99

[2]

ChiriacoM, SalfaI, Di MatteoG, et al.. Chronic granulomatous disease: clinical, molecular, and therapeutic aspects. Pediatr Allergy Immunol, 2016, 27(3): 242-253

[3]

RaptakiM, VarelaI, SpanouK, et al.. Chronic granulomatous disease: a 25-year patient registry based on a multistep diagnostic procedure, from the referral center for primary immunodeficiencies in Greece. J Clin Immunol, 2013, 33(8): 1302-1309

[4]

SegalBH, RomaniL, PuccettiP. Chronic granulomatous disease. Cell Mol Life Sci, 2009, 66(4): 553-558

[5]

KaneganeH, HoshinoA, OkanoT, et al.. Flow cytometry-based diagnosis of primary immunodeficiency diseases. Allergol Int, 2018, 67(1): 43-54

[6]

YingW, SunJ, LiuD, et al.. Clinical characteristics and immunogenetics of BCGosis/BCGitis in Chinese children: a 6 year follow-up study. PLoS One, 2014, 9(4): e94485

[7]

YangX, NongG, JiangM. Clinical features and flow cytometry assay of 2 chronic granulomatous disease. Guang Xi Yi Ke Da Xue Xue Bao (Chinese), 2011, 28(3): 382-385

[8]

LongZ, LiuH, LuS. Case report of one child with disseminated Baeille Calmette Gu6rin disease and CGD. Shi Yong Yi Xue Za Zhi (Chinese), 2012, 28(21): 3677-3688

[9]

GeC, LiY, JiangL. X-linked chronic granulomatous diseases: case report and literature review. J Mod Med Health, 2015, 31(9): 1437-1437

[10]

HeJ, GuoY, FengX, et al.. Chronic granulomatous disease and Mcleod syndrome caused by continuous X chromosome deletion: a report of two cases and literature review. Lin Chuang Er Ke Za Zhi (Chinese), 2016, 34(8): 614-617

[11]

LuX, JiangL, WangJ. The analysis of clinical manifestations and genetic mutations in childhood chronic granulomatous disease. Lin Chuang Er Ke Za Zhi (Chinese), 2016, 34(3): 204-207

[12]

ZhengB, ZhuC. Chronic granulomatous diseases in three children and literature review. Bei Jing Yi Xue (Chinese), 2016, 38(8): 785-788

[13]

QinM, WangH, QiaoC, et al.. Case report of one X-CGD child with purulent meningitis. Xin Yi Xue (Chinese), 2000, 31(2): 113

[14]

LiuH, SunZ, JinY, et al.. X-Linked chronic granulomatous diseases: case report and literature review. Zhong Guo Xiao Er Ji Jiu Yi Xue (Chinese), 2015, 22(7): 521-522

[15]

WuH, DongS, LiuJ, et al.. Four cases of neonatal X-linked chronic granulomatous disease and literature review. Zhong Guo Xin Sheng Er Ke Za Zhi (Chinese), 2014, 29(5): 302-305

[16]

HuangH, YangJ, HeT, et al.. One case of neonatal X-linked chronic granulomatous disease and literature review. Zhong Guo Xiao Er Ji Jiu Yi Xue (Chinese), 2014, 21(11): 710-712

[17]

YangZ, WangY, WangF. Clinical features and CYBB gene mutation analysis of chronic granulomatous disease in 6 neonate infants. Zhong Hua Shi Yong Er Ke Lin Chuang Za Zhi (Chinese), 2014, 29(20): 1556-1559

[18]

YangJ, WangGB, HuangHJ, et al.. X-linked chronic granulomatous disease family caused by anmino acid missing mutation in the gp91phox of flavocytochrome b558. Zhong Hua Fu You Lin Chuang Za Zhi (Chinese), 2006, 2(3): 137-139

[19]

LiSJ, JiangLP, LiuW, et al.. Clinical analysis of X-linked chronic granulomatous disease in 12 patients. Lin Chuang Er Ke Za Zhi (Chinese), 2011, 29(1): 46-50

[20]

GanZ, ZhuJ, LiC, et al.. One case report of X-linked chronic granulomatous disease. Lin Chuang Fang She Xue Za Zhi (Chinese), 2000, 19(10): 666-667

[21]

XiaoZ, ZhangL, MaL. One case report of X-linked chronic granulomatous disease. Lin Chuang Pi Fu Ke Za Zhi (Chinese), 2012, 41(9): 554-555

[22]

CuiZ, ShiX, PuF. One child with CGD misdiagnosed as bronchopneumonitis. Zhong Guo Yi Nan Za Zheng Za Zhi (Chinese), 2012, 11(6): 476

[23]

LiXQ, LiD, DuanMY, et al.. Clinical analysis of 8 cases with primary immunodeficiency disease in children. Zhong Guo Fu You Jian Kang Yan Jiu Za Zhi (Chinese), 2013, 24(5): 679-681

[24]

HeJX, LiuJ, LiuXY, et al.. Burkholderia cepacia infections in children with X-linked chronic granulomatous disease. Zhong Guo Shi Yong Er Ke Za Zhi (Chinese), 2012, 27(5): 381-383

[25]

HeJX, ZhaoSY, JiangZF. Recurrent pulmonary infections in pediatric patients with X-linked recessive chronic granulomatous disease:analysis of 3 cases. Zhong Guo Shi Yong Er Ke Za Zhi (Chinese), 2008, 23(8): 605-608

[26]

ZhaoW, KongX, WuJ. A patient with chronic granulomatous disease. Zhonghua Er Ke Za Zhi (Chinese), 2000, 38(7): 438

[27]

XuH, TianW, LiSJ, et al.. Clinical and molecular features of 38 children with chronic granulomatous disease in mainland China. J Clin Immunol, 2014, 34(6): 633-641

[28]

WuJ, WangWF, ZhangYD, et al.. Clinical features and genetic analysis of 48 patients with chronic granulomatous disease in a single center study from Shanghai, China (2005–2015): new studies and a literature review. J Immunol Res, 2017, 2017: 8745254

[29]

RawatA, VigneshP, SharmaA, et al.. Infection profile in chronic granulomatous disease: a 23-year experience from a tertiary care center in North India. J Clin Immunol, 2017, 37(3): 319-328

[30]

WinkelsteinJA, MarinoMC, JohnstonRB, et al.. Chronic granulomatous disease: report on a national registry of 368 patients. Medicine, 2000, 79(3): 155-169

[31]

van den BergJM, van KoppenE, ÅhlinA, et al.. Chronic granulomatous disease: the European experience. PLoS One, 2009, 4(4): e5234

[32]

WolachB, GavrieliR, de BoerM, et al.. Chronic granulomatous disease: clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patients. Am J Hematol, 2017, 92(1): 28-36

AI Summary AI Mindmap
PDF

90

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/