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Annex 5 (A5). Supplemental tables: Endo-Periodontal Lesion.

Table A5.1. Risk factors reported in the studies, stratified by study design.

Risk factors (% of studies according to each design)


Number Number of
Study Porcelain-
of Reference teeth Furcation Post- Carious
design Grooves Trauma fused-to- Periodontitis
studies included involvement preparation lesions
metal crowns

Clinical Didilescu 1, Gomes 2, Kipioti 3,


7 170 0.0 0.0 0.0 0.0 0.0 0.0 100
study Kobayashi 4, Li 5, Pereira 6, Rupf 7

Asgary 8, Attam 9, Ballal 10, Blanchard


11
, Castelo-Baz 12, Coraini 13, Floratos
14
, Gandhi 15, Goyal 16, Kambale 17,
Case
20 Karabucak 18, Kerezoudis 19, Kishan 30 50.0 20.0 20.0 20.0 10.0 10.0 0.0
report 20
, Mali 21, Miao 22, Oh 23, Pickel 24,
Sharma 25, Tobón-Arroyave 26, White
27

FINAL TOTAL Number of studies: 27 200 37.0 14.8 14.8 14.8 7.4 7.4 25.9

Table A5.2. Studied that evaluated the microbiota of endo-periodontal lesions.


Number of Periodontitis
Reference Study design Technique Main finding
teeth studied patient
The majority of isolates in periodontal pockets and root canals were
Kipioti 3 Clinical study 16 Culture Yes Bacteroides gingivalis (currently Porphyromonas gingivalis) and Bacteroides
melaninogenicus ss intermedius (currently Prevotella intermedia).
The predominant bacterial species in periodontal pockets and root canals
Kobayashi 4 Clinical study 15 Culture Yes were from the genera Streptococcus, Peptostreptococcus, Eubacterium,
Bacteroides, Fusobacterium, Actinomyces and Streptococcus.
The most prevalent species in periodontal pockets and root canals were
Pereira 6 Clinical study 27 Culture/ PCR Yes
Porphyromonas gingivalis, Prevotella intermedia and Prevotella nigrescens.
The predominant bacterial species in periodontal pockets and root canals
PCR/Checkerboard
were Fusobacterium nucleatum, Campylobacter rectus, Eubacterium
Didilescu 1 Clinical study 46 DNA-DNA Yes
nodatum, Eikenella corrodens, Parvimonas micra and Capnocytophaga
Hybridization
sputigena.
The similarity of bacteria in dental plaque and necrotic pulp ranged from
13.1% to 62.5%. The main genera identified in dental plaque were
PCR/ DGGE, cloning
Xia 28 Clinical study 13 No Campylobacter, Fusobacterium, Neisseria, Peptostreptococcus, Veillonella,
and sequencing
Aggregatibacter, Enterobacter and Haemophilus, and in necrotic pulps were
Mogibacterium, Corynebacterium, Neisseria and Actinomyces
The predominant bacterial species in periodontal pockets and root canals
PCR/ DGGE, cloning
Li 5 Clinical study 20 Yes were Filifactor alocis, Parvimonas micra, Porphyromonas gingivalis and
and sequencing
Tannerella forsythia.
The most prevalent bacterial species in periodontal pockets and root canals
were Aggregatibacter actinomycetemcomitans, Tannerella forsythia,
Rupf 7 Clinical study 31 Real Time PCR Yes
Eikenella corrodens, Fusobacterium nucleatum, Prevotella intermedia,
Porphyromonas gingivalis and Treponema denticola.
Enterococcus faecalis, Parvimonas micra, Filifactor alocis were among the
most prevalent species in both root canals and periodontal pockets. Other
Next Generation
Gomes 2 Clinical study 15 Yes species were also predominant in root canals (Mogibacterium timidum,
Sequencing
Fretibacterium fastidiosum) or in periodontal pockets (Streptococcus
constellatus, Eubacterium brachy, Tannerella forsythia).
PCR: Polymerase Chain Reaction, DGGE: denaturing gradient gel electrophoresis
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