Summary & Overview
CPT 0258U: Mind.Px Psoriasis NGS Gene Expression Assay
CPT code 0258U designates Mind.Px, a proprietary next-generation sequencing (NGS) gene expression assay produced by Mindera Corporation for use on psoriasis skin specimens collected with a proprietary patch. As a PLA code tied to a single manufacturer and test, it captures a targeted 50–100 gene expression profile and uses algorithmic interpretation to inform medication selection for psoriasis. Nationally, PLA codes like 0258U matter because they codify unique, commercially available molecular diagnostics and enable standardized billing and reporting for precision medicine tools.
Key payers examined include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of clinical purpose and service delivery, payer coverage context, typical sites of service, and common billing modifiers associated with laboratory services. The publication summarizes benchmark considerations for proprietary molecular assays, highlights policy and coding implications for single-source tests, and presents clinical context for use in treatment selection for psoriasis.
This report is intended for revenue cycle professionals, laboratory directors, clinicians ordering molecular diagnostics, and policy analysts seeking a national view of how a PLA-coded psoriasis gene expression test is described and classified for billing and coverage discussion.
Billing Code Overview
CPT code 0258U is a Proprietary Laboratory Analyses (PLA) code for the Mind.Px test manufactured by Mindera Corporation. The assay is performed on a psoriasis skin specimen collected with a proprietary patch that captures RNA from the lesion. The test uses next-generation sequencing (NGS) to evaluate gene expression across a targeted panel of 50 to 100 genes and applies an algorithmic analysis to aid in selecting appropriate medication for psoriasis treatment.
Service type: Laboratory — molecular diagnostic, proprietary gene expression assay
Typical site of service: Clinical laboratory or reference lab
Clinical & Coding Specifications
Clinical Context
A 38-year-old patient with moderate-to-severe plaque psoriasis presents to a dermatology clinic after inadequate response to first-line topical therapies and phototherapy. The dermatologist evaluates the active lesion and determines that molecular profiling of the lesional skin may help guide systemic or biologic therapy selection. A proprietary collection patch designed to capture RNA from the psoriasis lesion is applied to the affected skin in clinic; the patch is removed per manufacturer instructions and the specimen is sent to the manufacturer-specific laboratory (Mindera Corporation) for the Mind.Px test. The laboratory performs next-generation sequencing (NGS)–based gene expression analysis of a focused panel (50–100 genes) and algorithmic interpretation to identify medication-response signatures. Results are returned to the ordering dermatologist, who integrates the report with clinical history, prior treatment response, and comorbidities to inform selection of a systemic agent or biologic. Typical site of service is an outpatient dermatology clinic or ambulatory surgical center for specimen collection; laboratory processing occurs at the vendor’s central lab. Service type: Proprietary Laboratory Analyses (PLA) molecular diagnostic test using NGS-based gene expression profiling on a psoriasis skin specimen collected with a proprietary patch.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
00 | No modifier — standard reporting | Use when no special circumstances apply. |