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. 2016 Nov 28;16:165. doi: 10.1186/s12890-016-0332-z

Table 2.

Case–control studies evaluating the role of P. acnes in sarcoidosis

First author/Year (Ref.) Country Molecular technique Sarcoidosis Controls OR (95% CI)
n/N n/N
Robinson, 2013 [24] USA PCR for bacterial 16S rDNA 7/30 1/30 8.83 (1.01–76.96)
Oswald-Richter, 2012 [25] USA MALDI-IMS for propionibacterial proteins 7/15 1/4 2.63 (0.22–31.35)
Yasuhara, 2005 [31] Japan PCR for 16S rRNA 2/6 0/6 7.22 (0.28–189.19)
Gazouli, 2002 [22] Greece PCR for 16S rRNA 0/46 0/20 -
Eish, 2002 [35] Japan PCR for 16S rRNA 93/108 25/86 15.13 (7.39–30.99)
Ishige, 1999 [38] Japan Quantitative PCR for 16S rRNA 12/15 3/15 16 (2.67–95.75)
Negi, 2012 [56] Japan Immunohistochemical methods (PAG and TIG antibodies) and western blot 149/196 0/79 500.43 (30.44–8226.20)
Yamada, 2002 [57] Japan Quantitative real-time PCR for 16S rRNA 8/9 2/9 28 (2.07–379.25)
Eishi, 1994 [58] Japan PCR for P. acnes DNA 36/39 12/29 17 (4.23–68.28)
Abe, 1984 [19] Japan Isolation of P acnes in culture 31/40 38/180 12.87 (5.65–29.34)
Hiramatsu, 2003 [59] Japan Nested PCR for 16S rRNA 21/30 7/30 7.67 (2.42–24.24)

16S rDNA ribosomal DNA, MALDI-IMS matrix-assisted laser desorption ionization as a mass spectrometry imaging, rRNA ribosomal RNA