Table Info

Table 3.

Differences between patients with false positive and negative serological test

Variable	Negative serology (mean ± SD)	False positive serology (mean ± SD)	P value
Direct bilirubin (mg/dL)	0.13 ± 6.04	0.25 ± 0.26	0.16
indirect bilirubin (mg/dL)	0.58 ± 0,19	0.75 ± 0,44	0.25
GOT (U/L)	38.46 ± 5.8	41.85 ± 8.00	0.73
GPT (U/L)	37.69 ± 24,69	45.57 ± 20.65	0.48
GGT (U/L)	57.69 ± 38.15	140.85 ± 82.9	0.03^*
ALP (U/L)	107.92 ± 43.67	149.57 ± 78.84	0.16
CRP (mg/L)	1.73 ± 1.70	8.67 ± 8.96	0.01^*
ESR (mm/h)	28.46 ± 25.49	25.42 ± 13.56	0.77
Gamma globulin (%)	0.18 ± 6.28	0.21 ± 9.46	0.44
	N (%)	N (%)
ANA⁺	20 (76.92%)	8 (57.14%)	n.s.
AMA⁺	8 (30.77%)	8 (57.14%)	n.s.
Anti-LKM⁺	2 (7.69%)	0 (0%)	n.s.
ASMA⁺	8 (30.76%)	4 (28.57%)	n.s.
ANCA⁺	4 (15.38%)	0 (0%)	n.s.
Polyclonal hypergammaglobulinemia	12 (46.15%)	6 (42.86 %)	n.s.

Significant P value; n.s.: non significant P value

Declarations

Author contributions

MGC contributed to data collection, study design and paper draft; MS performed the analysis and contributed to study design and paper draft; RV, FC, GDG and PC organized the database and revised sections of the manuscript; GS conceptualized and supervised the entire work.

Conflicts of interest

The authors declare that they have no conflicts of interest.

Ethical approval

All the procedures performed in this study involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

Consent to participate

Informed consent to participate in the study was obtained from all participants.

Consent to publication

Not applicable.

Availability of data and materials

All relevant data is contained within the manuscript.

Funding

Not applicable.

Copyright

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