10.1 Anatomy of the Periodontium and Biologic Width

Key Takeaways

  • The supracrestal tissue attachment (historically termed biologic width) averages 2.04 mm in human histology (junctional epithelium 0.97 mm and connective tissue attachment 1.07 mm), requiring a minimum 3.0 mm clearance between restorative finish lines and the alveolar crest to prevent localized chronic inflammation and osteoclastic bone loss.

  • The oblique fiber group is the largest and most abundant principal fiber group of the periodontal ligament (PDL), inserting diagonally from root cementum coronally into the alveolar socket wall to convert vertical axial masticatory compressive loads into physiological tensile strain on bundle bone.

  • The width of attached gingiva is greatest in the maxillary incisors (3.5 to 4.5 mm) and mandibular incisors (3.3 to 3.9 mm), and narrowest in the premolars (mandibular first premolar ~1.8 mm, maxillary first premolar ~1.9 mm); palatal gingiva lacks a mucogingival junction, transitioning seamlessly into the masticatory mucosa of the hard palate.

  • The junctional epithelium forms an organic attachment to enamel or cementum via hemidesmosomes and an internal basal lamina, displaying rapid cellular turnover (4 to 6 days) and wide intercellular spaces (~18% volume) that allow continuous transmigration of neutrophils and flow of gingival crevicular fluid.

  • The interdental col is a non-keratinized, saddle-shaped epithelial depression apical to the interproximal contact area connecting facial and lingual papillae, representing the most vulnerable anatomical site for plaque accumulation and the initial breakdown of gingivitis.

Last updated: October 2026

The periodontium constitutes the biological functional unit supporting and anchoring the tooth within the maxillary and mandibular alveolar processes. It comprises four distinct tissues: two soft tissue compartments (gingiva and periodontal ligament) and two mineralized compartments (root cementum and alveolar bone). A rigorous mastery of periodontal microanatomy, cellular turnover, biomechanical stress distribution, and histological dimensions—specifically the supracrestal tissue attachment (biologic width)—is foundational for clinical periodontics, restorative dentistry, and the Saudi Dental Licensure Examination (SDLE / SPLE).


Macroscopic and Microscopic Gingival Anatomy

The gingiva forms the mucosal collar surrounding the cervical necks of erupted teeth and overlying the coronal alveolar bone. Macroscopically, it is divided into the free (marginal) gingiva, the attached gingiva, and the interdental papillae.

                   CORONAL-APICAL GINGIVAL ARCHITECTURE

          Gingival Margin
                │ 
                ├── Free (Marginal) Gingiva (Unattached, ~1.0-1.5 mm)
          Free Gingival Groove
                │ 
                ├── Attached Gingiva (Bound to periosteum & cementum)
                │   - Maxillary Incisors: 3.5 - 4.5 mm (Widest)
                │   - Mandibular Premolars: ~1.8 mm (Narrowest)
          Mucogingival Junction (MGJ) [Absent on Palate]
                │ 
                └── Alveolar Mucosa (Mobile, non-keratinized, elastic)

1. Oral (Outer) Epithelium

  • Histology: Keratinized or parakeratinized stratified squamous epithelium, approximately 0.2 to 0.3 mm thick.
  • Architecture: Characterized by prominent, undulating epithelial ridges (rete pegs) that interdigitate deeply with underlying connective tissue papillae. This structural interdigitation resists heavy mechanical shearing forces during mastication and gives healthy attached gingiva its characteristic clinical "stippled" (orange-peel) texture in approximately 40% of adults.
  • Cellular Layers: Stratum basale (cuboidal progenitor cells undergoing mitosis), stratum spinosum (polyhedral cells rich in desmosomes), stratum granulosum (flattened cells containing keratohyalin granules), and stratum corneum (cornified, flattened squames lacking nuclei in orthokeratinized variants). Non-keratinocyte cells include dendritic Langerhans cells (antigen-presenting immune cells), melanocytes (melanin synthesis), and Merkel cells (tactile mechanoreception).
  • Turnover Rate: The oral epithelium undergoes physiological cellular renewal every 10 to 14 days.

2. Sulcular Epithelium

  • Histology: Thin, non-keratinized stratified squamous epithelium lining the shallow gingival sulcus from the crest of the gingival margin to the coronal limit of the junctional epithelium.
  • Barrier Characteristics: In pristine health, the sulcular epithelium lacks rete pegs. It functions as a semipermeable membrane; however, under the influence of subgingival biofilm accumulation, inflammatory mediators induce micro-ulcerations, vascular engorgement, and irregular rete peg proliferation into the inflamed lamina propria, manifesting clinically as bleeding on probing (BOP).

3. Junctional Epithelium (JE)

  • Histology and Attachment: Non-keratinized stratified squamous epithelium forming an organic biological seal around the tooth neck. It is 15 to 30 cells thick coronally and tapers apically to a thin wedge only 1 to 3 cells thick at its termination at the cementoenamel junction (CEJ).
  • Dual Basal Lamina System:
    • Internal Basal Lamina (IBL): Fastens the junctional epithelium directly to the calcified tooth structure (enamel, cementum, or exposed dentin) via hemidesmosomes. It consists of a lamina lucida (rich in laminin-332, formerly laminin-5) and a lamina densa directly abutting the mineralized surface.
    • External Basal Lamina (EBL): Connects the basal cell layer of the junctional epithelium to the underlying gingival connective tissue via hemidesmosomes.
  • Exceptional Cellular Turnover: Possesses the most rapid cellular turnover of any oral tissue—renewing completely every 4 to 6 days. Basal cells divide actively, migrate coronally, and desquamate into the gingival sulcus.
  • Permeability & Host Defense: Wide intercellular spaces occupy approximately 18% of the tissue volume (compared to only ~3% in oral epithelium), mediated by fewer desmosomal junctions. This loose intercellular architecture permits:
    1. The rapid, continuous outward outflow of gingival crevicular fluid (GCF) carrying host defense immunoglobulins (predominantly IgG), complement components, and antimicrobial peptides.
    2. The rapid forward transmigration of polymorphonuclear neutrophils (PMNs) from the connective tissue vascular plexus into the sulcus as the first cellular defense barrier against subgingival microbial biofilms.

4. Attached Gingiva Dimensions

  • Definition: The portion of gingiva that is firmly bound to the underlying cementum and alveolar bone periosteum, extending from the projection of the base of the gingival sulcus (or pocket) to the mucogingival junction (MGJ).
  • Anatomical Distribution:
    • Maxillary arch: Widest over the central and lateral incisors (3.5 to 4.5 mm); decreases posteriorly to its narrowest band over the first premolars (~1.9 mm).
    • Mandibular arch: Widest over the incisors (3.3 to 3.9 mm); narrowest at the facial aspect of the first premolars (~1.8 mm).
  • Clinical Significance: A minimum band of ≥2 mm\ge 2\text{ mm} of keratinized gingiva (corresponding to ≥1 mm\ge 1\text{ mm} of firmly attached gingiva) was historically considered necessary (Lang and Löe, 1972) to maintain periodontal health and prevent recession, especially around subgingival restorative margins or orthodontic movement sites.
  • Palatal Aspect: The palatal gingiva exhibits no mucogingival junction because it blends seamlessly into the dense, firmly bound orthokeratinized masticatory mucosa covering the hard palate.

5. The Interdental Col

  • A concave, saddle-shaped depression connecting the facial and lingual interdental papillae beneath the interproximal contact point of adjacent teeth.
  • Epithelial Structure: Covered entirely by thin, non-keratinized stratified squamous epithelium derived from reduced enamel epithelium during tooth eruption.
  • Pathological Vulnerability: Because it lacks protective keratinization, is inaccessible to natural salivary flushing, and traps bacterial debris beneath proximal contact areas, the col represents the primary initial site of inflammatory breakdown in plaque-induced gingivitis.

Principal Gingival Fiber Groups (Lamina Propria)

The gingival connective tissue core (lamina propria) is composed predominantly of densely organized Type I (60% to 70%) and Type III (20% to 30%) collagen bundles arranged in distinct functional groups:

  1. Dentogingival Fibers: Radiate fan-like from the root cementum just beneath the junctional epithelium into the lamina propria of the free and attached gingiva.
  2. Alveologingival Fibers: Arise from the crest of the alveolar bone and course coronally into the free and attached gingival stroma.
  3. Circular Fibers: Encircle the cervical collar of the tooth in a continuous ring within the free marginal gingiva, maintaining marginal adaptation against displacement.
  4. Dentoperiosteal Fibers: Extend from cervical cementum over the buccal and lingual alveolar bone crests, inserting into the periosteum of the alveolar cortical plate.
  5. Transseptal Fibers ("The Interdental Ligament"): Extend interproximally over the interdental alveolar bone crest, inserting into the cementum of adjacent teeth. They maintain interdental arch continuity and space relationships.
    • Orthodontic Memory & Relapse: Transseptal fibers exhibit extremely slow metabolic turnover. Following orthodontic de-rotation of crowded teeth, residual supracrestal elastic recoil in transseptal fibers drives rapid rotational relapse.
    • Circumferential Supracrestal Fiberotomy (CSF / Edwards Procedure): Surgical severance of transseptal and free gingival fibers down to the crest of bone eliminates this elastic recoil, permanently stabilizing corrected orthodontic rotations.

Periodontal Ligament (PDL): Biology and Biomechanics

The periodontal ligament is a specialized, hourglass-shaped vascular fibrous connective tissue occupying the space between the root cementum and the alveolar bundle bone.

                    PDL HOURGLASS THICKNESS PROFILE

             Alveolar Crest: ~0.20 mm
                    │
                    ▼
             Mid-Root Fulcrum: ~0.15 mm (Narrowest, rotational center)
                    ▲
                    │
             Root Apex: ~0.25 mm
  • Physical Dimensions: Measures approximately 0.15 to 0.38 mm in width. It is thinnest at the mid-root level (~0.15 mm), which serves as the physiological fulcrum for tilting and rotational tooth movements, and widest at the coronal crest (~0.20 mm) and apical base (~0.25 mm).

1. Principal Fiber Groups of the PDL

The principal collagen bundles insert into root cementum on one side and bundle bone on the other; the mineralized, embedded terminal ends are termed Sharpey's fibers.

  • Alveolar Crest Fibers: Extend obliquely downward and outward from cervical cementum just below the CEJ to the alveolar crest. Function: resist lateral and tipping forces, prevent tooth extrusion.
  • Horizontal Fibers: Run perpendicularly at right angles to the long axis from cementum to alveolar bone in the coronal third of the PDL. Function: resist horizontal and lateral forces.
  • Oblique Fibers (The Largest Group): Run diagonally in a coronal direction from root cementum into the alveolar bone wall, constituting over two-thirds of all PDL fibers.
    • Biomechanical Action: They form the primary load-bearing suspensory mechanism. When axial compressive loads strike the tooth during mastication, the tooth is pushed into the socket, putting oblique fibers under tension. This converts vertical compressive forces into physiological tensile strain on the alveolar bundle bone, stimulating bone preservation rather than destructive osteoclastic resorption.
  • Apical Fibers: Radiate from cementum at the root apex to the fundus of the socket. Function: cushion against vertical compressive loads and resist luxation/extrusion.
  • Interradicular Fibers: Located exclusively in the furcation areas of multirooted teeth (e.g., teeth 16, 26, 36, 46). Function: resist rotational torque, lateral tipping, and vertical displacement.

2. Cellular Constituents of the PDL

  • Fibroblasts (65% of PDL cells): Primary functional cells responsible for both the synthesis and degradation of collagen via phagocytosis and intracellular digestion, ensuring continuous, rapid collagen remodeling.
  • Cementoblasts & Cementoclasts: Reside along the cemental surface; synthesize cementoid and resorb cementum during trauma.
  • Osteoblasts & Osteoclasts: Line the cribriform plate; mediate bone apposition and resorption in response to functional loading and orthodontic force.
  • Epithelial Rests of Malassez (ERM): Discrete clusters of dormant epithelial cell remnants of Hertwig's epithelial root sheath (HERS) located within the PDL space. Under the stimulation of chronic bacterial inflammation (such as a non-vital periapical granuloma), ERM proliferate to form the epithelial lining of radicular (periapical) cysts or developmental lateral periodontal cysts.
  • Undifferentiated Mesenchymal Progenitor Cells: Multipotent stem cells capable of differentiating into fibroblasts, osteoblasts, or cementoblasts during tissue repair and periodontal regeneration.

3. Neurovascular Supply & Proprioception

  • Blood is supplied via three pathways: apical vessels entering through the apical foramen, interalveolar perforating arteries passing through the cribriform plate (Volkmann's canals), and coronal anastomoses from gingival vessels.
  • Richly innervated by myelinated and unmyelinated mechanoreceptors (predominantly Ruffini-like endings) that detect minute occlusal displacements (>1 to 2 μm\mu\text{m}). These provide dynamic proprioceptive feedback that reflexively inhibits elevator masticatory muscles (masseter, temporalis) during unexpected hard contact, protecting teeth and the TMJ from traumatic fracture.

Root Cementum: Classifications and Dynamics

Cementum is an avascular, non-innervated, mineralized mesenchymal tissue covering the anatomical root. It consists of 45% to 50% inorganic hydroxyapatite crystals and 50% to 55% organic matrix (predominantly Type I collagen) and water.

Schroeder's Cementum Classification

  1. Acellular Afibrillar Cementum (AAC): Found exclusively at the cervical enamel margin; contains no collagen fibers and no cells. Formed during tooth eruption when reduced enamel epithelium degenerates prematurely.
  2. Acellular Extrinsic Fiber Cementum (AEFC / Primary Cementum): Covers the coronal and middle two-thirds of the root. Contains densely packed, oriented extrinsic collagen fibers (Sharpey's fibers) running perpendicular to the root surface, synthesized prior to functional tooth eruption. It is the primary tissue anchoring the tooth to the PDL.
  3. Cellular Intrinsic Fiber Cementum (CIFC): Contains cementocytes in lacunae; collagen fibers are intrinsic (synthesized by cementoblasts) and run parallel to the root surface. Lacks Sharpey's fibers and plays a purely reparative role in filling resorption lacunae.
  4. Cellular Mixed Stratified Cementum (CMSC / Secondary Cementum): Found in the apical third of roots and within multirooted furcations. Composed of alternating layers of acellular extrinsic and cellular intrinsic cementum. Exhibits continuous lifelong compensatory deposition to counterbalance occlusal crown wear and maintain vertical dimension.

Cementoenamel Junction (CEJ) Relationships (Choquet's Data)

  • Overlap (60% to 65% of cases): Cementum overlaps the cervical enamel edge.
  • Edge-to-Edge (30% of cases): Cementum and enamel meet in a sharp, continuous line.
  • Gap (5% to 10% of cases): Cementum and enamel fail to meet, leaving an area of exposed, unmineralized dentin. This anatomical gap is the primary clinical etiology of cervical dentin hypersensitivity and predisposes the site to rapid root caries and abrasion lesions.

Alveolar Process: Bundle Bone and Cortical Plates

The alveolar process is the tooth-dependent bony ridge housing the alveoli (sockets).

  • Bundle Bone (Alveolar Bone Proper): The thin compact bone lining the inner socket wall into which Sharpey's fibers embed. In clinical radiography, this layer appears as a radiopaque line termed the lamina dura. Histologically, it is perforated by numerous nutrient Volkmann's canals transmitting blood vessels and nerves into the PDL, earning it the anatomic designation cribriform plate.
  • Cortical Plates: Dense outer compact bone plates (facial and lingual). The mandibular buccal cortical plate is substantially thicker than the maxillary plate, reaching its maximum density at the external oblique ridge (buccal shelf) adjacent to teeth 46 and 47.
  • Spongiosa (Cancellous Bone): Trabecular bone located between the lamina dura and outer cortical plates, containing active hematopoietic or fatty marrow.
  • Dehiscence vs. Fenestration:
    • Dehiscence: A localized loss of marginal cortical bone exposing the cervical root surface, producing a V-shaped marginal cleft extending to the crest.
    • Fenestration: An isolated "window" defect in the cortical bone exposing the root surface, while the marginal bone crest remains intact. More common on prominent facial roots with thin biotypes (e.g., maxillary canines and premolars).

Biologic Width (Supracrestal Tissue Attachment)

In 1961, Gargiulo, Wentz, and Orban established the fundamental mean dimensions of the dentogingival junction in human autopsy specimens (corroborated by Vacek et al., 1994). In the 2017 AAP/EFP World Workshop, this anatomical complex was formally renamed the Supracrestal Tissue Attachment (STA).

              HISTOLOGICAL SUPRACRESTAL TISSUE ATTACHMENT
 
   [Gingival Margin]
          │
          │   Physiological Gingival Sulcus (~0.69 - 1.0 mm)
          ▼
   [Coronal Margin of JE]
          │
          │   Junctional Epithelium (0.97 mm)  ┐
          ▼                                    ├─ Biologic Width (2.04 mm)
   [Cementoenamel Junction]                    │  (Supracrestal Attachment)
          │                                    │
          │   Connective Tissue (1.07 mm)      ┘
          ▼
   [Alveolar Bone Crest]

1. Histological Dimensions

  • Physiological Sulcus Depth: Mean 0.69 mm (clinically probed at 1.0 to 1.5 mm).
  • Junctional Epithelial Attachment: Mean 0.97 mm (range 0.71 to 1.35 mm).
  • Connective Tissue Attachment: Mean 1.07 mm (range 1.06 to 1.08 mm).
    • The connective tissue attachment is the most anatomically constant dimension of the entire periodontium.
  • Total Supracrestal Tissue Attachment (Biologic Width): Mean 2.04 mm (0.97 mm + 1.07 mm).

2. The 3.0 mm Clinical Margin Rule

To maintain biological equilibrium, any restorative finish line (crown margin, veneer margin, or subgingival restoration) must terminate at least 3.0 mm coronal to the alveolar bone crest: Required Distance=Supracrestal Attachment (2.0 mm)+Sulcus Depth/Safety Margin (1.0 mm)=3.0 mm\text{Required Distance} = \text{Supracrestal Attachment }(2.0\text{ mm}) + \text{Sulcus Depth/Safety Margin }(1.0\text{ mm}) = 3.0\text{ mm}

Important

If a subgingival restoration margin is placed closer than 3.0 mm to the bone crest (impinging on the junctional epithelium or connective tissue fibers), biological space is invaded. The host tissue mounts a severe localized inflammatory reaction characterized by persistent erythema, chronic bleeding on probing, and osteoclastic bone resorption as the body attempts to recreate space for connective tissue fiber insertion.

3. Biotype-Specific Pathological Sequelae of Violation

  • Thin Periodontal Biotype: Characterized by delicate, thin alveolar bone plates and narrow scalloped gingiva. Biologic width impingement leads to rapid, unesthetic gingival recession and root exposure.
  • Thick-Flat Periodontal Biotype: Characterized by dense, thick cortical bone and heavy, fibrotic attached gingiva. Biologic width impingement triggers intractable chronic pocketing, continuous bleeding, edema, and recurrent periodontal abscesses without immediate recession.

4. Corrective Clinical Interventions

When caries, root fractures, or restorative margins violate the supracrestal tissue attachment, two definitive corrective modalities are indicated:

  • Surgical Crown Lengthening: Resective osseous surgery involving ostectomy (removal of supporting bundle bone) and osteoplasty (recontouring non-supporting bone) to re-establish ≥3.0 mm\ge 3.0\text{ mm} between the future restorative finish line and the new alveolar crest. In addition, an adequate coronal ferrule (≥1.5\ge 1.5 to 2.0 mm2.0\text{ mm} of sound vertical dentin wall height with ≥1.0 mm\ge 1.0\text{ mm} thickness) must be preserved for long-term crown retention.
  • Orthodontic Extrusion (Forced Eruption): Indicated in esthetically critical anterior zones (e.g., teeth 11, 21) where osseous resection would cause unacceptable gingival margin discrepancies relative to adjacent teeth.
    • Rapid Extrusion with Fibrotomy: Roots are extruded rapidly while performing weekly supracrestal fiberotomies to sever the transseptal and gingival fibers. This allows the tooth to move coronally without pulling the alveolar bone crest and gingival margin along with it.

Summary of Periodontal Tissue Components & Clinical Dimensions

Tissue ComponentPrimary Cellular ElementsHistological / Clinical DimensionStructural Function & Biomechanical RoleSDLE Clinical Key Point
Oral EpitheliumKeratinocytes, Langerhans, Melanocytes, Merkel0.2 – 0.3 mm; turnover 10–14 daysResists masticatory friction; rete pegs produce gingival stipplingParakeratinized/orthokeratinized; protects underlying lamina propria
Junctional EpitheliumNon-keratinized squames, PMNs0.97 mm (coronal: 15–30 cells; apical: 1–3 cells); turnover 4–6 daysOrganic attachment via hemidesmosomes (IBL/EBL); egress for GCF and PMNsFastest turnover in oral cavity; wide intercellular spaces (~18% volume)
Connective Tissue (STA)Fibroblasts (65%), histiocytes, mast cells1.07 mm mean widthDensely cross-linked Type I collagen inserting directly into root cementumMost constant dimension of the supracrestal complex (biologic width)
Oblique PDL FibersFibroblasts, undifferentiated ectomesenchymeOccupies >66% of PDL fiber volumeRuns diagonally coronal from cementum to socket wallConverts axial compressive forces into physiological tensile stress on bone
Transseptal FibersFibroblasts, collagen bundlesTraverses interdental septumConnects adjacent root cementum coronal to bone crestResponsible for post-orthodontic rotational relapse; severed by CSF
AEFC (Primary Cementum)Acellular (formed before eruption)Coronal 2/3 of root; 20–50 μm\mu\text{m}Dense Sharpey's fibers perpendicular to root; primary functional tooth anchorAvascular, non-innervated; does not remodel under physiological loads
CMSC (Secondary Cementum)Cementocytes in lacunaeApical 1/3 and furcations; 150–200 μm\mu\text{m}Alternating intrinsic/extrinsic fibers; continuous lifelong depositionCompensates for occlusal wear/attrition to preserve vertical dimension
Bundle Bone (Lamina Dura)Osteoblasts, osteocytes, osteoclastsVariable; pierced by Volkmann's canalsThin compact bone socket wall; Sharpey's fibers anchor hereAppears radiopaque as lamina dura; loss signifies active periodontitis
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Supracrestal Tissue Attachment Violations & Crown Lengthening Decision Pathway
Test Your Knowledge

A 42-year-old female presents for the preparation of a full-coverage crown on tooth 14 (maxillary right first premolar). Because of a subgingival disto-cervical fracture extending 0.5 mm coronal to the alveolar bone crest, the clinician prepares the crown margin 1.0 mm coronal to the alveolar crest. Six months post-cementation, the patient returns complaining of persistent localized bleeding during brushing and dull discomfort. Clinical examination reveals localized 4 mm probing depths, severe erythema, and profuse bleeding on probing at the distobuccal margin of tooth 14. What is the primary biological etiology of these clinical findings?

A

Rupture of the transseptal gingival fiber network, causing immediate pathological tooth migration and secondary occlusal trauma.

B

Violation of the supracrestal tissue attachment (biologic width), causing chronic inflammation and bone resorption.

C

Cytotoxic allergic contact stomatitis induced by metal ions leaching from the underlying metal coping into the sulcular fluid.

D

Inadequate polymerization of the resin luting cement, resulting in excessive monomer leaching into the connective tissue attachment.

Test Your Knowledge

During mastication of a firm bolus of food, heavy axial compressive forces are directed along the long axis of tooth 36 (mandibular left first molar). Which principal fiber group of the periodontal ligament (PDL) constitutes the largest and primary load-bearing group responsible for absorbing these axial forces and converting them into tensile stress on the alveolar bundle bone?

A

Transseptal fiber group, traversing interproximally over the interdental septum between adjacent root cementum surfaces.

B

Alveolar crest fiber group, running apically from cervical cementum to the alveolar crest to resist extrusion.

C

Horizontal fiber group, extending at right angles between root cementum and the cribriform plate to counter lateral forces.

D

Oblique fiber group, coursing coronally and diagonally from root cementum to the surrounding alveolar socket wall.

Test Your Knowledge

A periodontist evaluates the gingival architecture of a 30-year-old patient prior to orthodontic therapy. Which clinical statement correctly describes the anatomical dimensions of the attached gingiva and interdental col in the permanent dentition?

A

The keratinized attached gingiva is widest in the incisor regions and narrowest on the facial aspect of the premolars.

B

The interdental col is covered by heavily orthokeratinized stratified squamous epithelium with deep rete pegs that resist bacterial invasion.

C

Palatal attached gingiva is demarcated by a distinct mucogingival junction located 3.0 mm apical to the palatal cervical margin.

D

Attached gingiva width is measured from the marginal gingival crest to the mucogingival junction, including the free gingival margin.

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