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Inflammation panel · pg/mL

VIP (Vasoactive Intestinal Polypeptide)

VIP (Vasoactive Intestinal Polypeptide) is a clinical biomarker on the Inflammation panel, reported in pg/mL. Standard reference range: 23–63 pg/mL. Functional (optimal) range used by integrative practitioners: 50–63 pg/mL.

What is VIP (Vasoactive Intestinal Polypeptide)?

VIP is a 28-amino acid neuropeptide produced by enteric, pulmonary (NANC), and SCN (suprachiasmatic nucleus) neurons. It is the primary endogenous NANC pulmonary vasodilator, an anti-inflammatory regulator (Th1/Th17 suppression, Treg induction), and the master coordinator of SCN-driven circadian coupling. VIP below 23 pg/mL is found in 98% of CIRS-WDB patients (N=1,829 Shoemaker case series); deficiency produces functional pulmonary hypertension, sleep dysregulation, and impaired MSH production through VPAC1/VPAC2 signaling.

Reference ranges

Range typeValue (pg/mL)Source
Standard (lab)23–63Typical Quest / LabCorp adult reference
Functional (optimal)50–63Integrative / functional medicine consensus

How SomaVue interprets VIP (Vasoactive Intestinal Polypeptide)

SomaVue maps every result for VIP (Vasoactive Intestinal Polypeptide) against four clinical lenses — nutrient cofactors, toxin exposure, infection drivers, and circadian/hormonal context — and connects each interpretation to specific peer-reviewed citations. Pre-mapped clinical reasoning and cross-marker pattern detection are available inside the practitioner workspace.

See the full interpretation

Upload a patient PDF or enter values manually to see the four-lens analysis, cross-marker patterns, and cited evidence for VIP (Vasoactive Intestinal Polypeptide) and 205 other markers.

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Educational reference only. Reference ranges vary by laboratory, assay method, age, sex, and clinical context. Functional ranges represent integrative-medicine consensus and are not regulatory thresholds. SomaVue does not diagnose, treat, mitigate, or prevent disease. Always consult a licensed healthcare provider.