02 · Make sense of your results

Understanding Your Sperm Tests

Sample collection, count, movement, shape, repeat testing, and what sperm DNA tests can and can’t tell you.

  • 8 minread
  • 4chapters
  • 4myths checked
  • 26sources
Start reading ↓
Watercolour illustration of a fertility laboratory microscope, closed sample container and stylised sperm cells
Illustrated concept · Fertility with Kara
In this guide

A report is a starting point.

Count, movement and shape answer different questions. Learn how to prepare for a sample, read the full pattern of results and ask whether repeat or additional testing would change your plan.

Prepare for the sample · Read the results in context · Weigh a sperm DNA test · Ask what comes next

Read alongside the female fertility guides

Preview for Kara’s review. Expanded educational draft · sources checked 12 October 2026 · clinical approval pending.

01 · Your test results

Reading a semen analysis without panic

Concentration describes sperm in each millilitre. Total sperm number describes the whole ejaculate. For example, 2 mL at 20 million sperm per mL gives approximately 40 million sperm in the sample. This is a counting example, not a pregnancy prediction.

Three illustrated panels showing sperm number, movement and shape

Count

How many sperm are present? Concentration and total number use different units.

Movement

How do sperm move? Progressive movement means moving forward.

Shape

What proportion meet laboratory shape criteria? Shape does not show DNA quality.

These measurements answer different questions. The artwork is conceptual and cannot be used to score a sample.

Motility describes movement. Progressive sperm move forward; non-progressive sperm move but make little useful forward progress. Total motility includes both categories. Vitality describes how many sperm are alive, which is useful when movement is very low.

Morphology is the proportion meeting strict shape criteria under a microscope. A result of 4% does not mean only 4% are alive or that 96% carry abnormal DNA. Shape assessment, vitality and DNA testing are different measurements. A low morphology result needs interpretation alongside the other findings.

The WHO reference values below are fifth-centile values from men whose partners conceived naturally within a year. About 5% of those men had results below each value. They describe a reference population; they are not a minimum required for pregnancy. A result above them does not guarantee conception. The reference group was about 3,500 men from 12 countries, and most of Africa was missing or under-represented.

Fertile and infertile men overlap a lot. In a large US comparison of about 1,500 men, many with “low” results had fathered children and some with “normal” results were struggling; no single measure was diagnostic. One man’s sperm count can also swing by half or more from one sample to the next, so one test is never the whole story.

Your laboratory’s methods, reference information, collection details, medical history and partner’s assessment all matter. Avoid turning a report into a personal score or comparing two laboratories as if every measurement were interchangeable.

WHO sixth edition (2021): lower reference values, not fertility cut-offs
MeasureReference valueWhat it describes
Volume1.4 mLAmount of semen
Concentration16 million/mLSperm in each millilitre
Total sperm number39 millionSperm in the whole ejaculate
Total motility42%Progressive + non-progressive movement
Progressive motility30%Sperm moving forward
Vitality54%Sperm that are alive
Morphology4%Sperm meeting strict shape criteria
What these numbers cannot tell you

They cannot diagnose infertility alone, measure your chance of pregnancy by themselves, or show that all sperm DNA is normal. Your own laboratory report and clinical assessment come first.

The key ideaStrong evidence: A guideline recommendation rated Strong (European or US urology guidelines), or a high- or moderate-certainty systematic review or randomised trial, with the major guidelines agreeing.

The WHO reference values describe the lowest 5% of men who recently fathered a child. They are a guide, not a pass-or-fail line.

Read more: WHO laboratory manual for human semen, sixth edition (2021) · Campbell et al. (2021): the data behind the WHO reference values · Guzick et al. (2001): semen results in fertile and infertile men · Keel (2006): how much one man’s results vary between samples · ASRM patient education: Sperm morphology (2023)

02 · Sample & repeat tests

Preparing for a sample and understanding repeats

Follow the instructions from the laboratory doing your test. WHO guidance specifies two to seven days without ejaculation before a diagnostic semen test. Longer abstinence is not automatically better, and instructions for fertility treatment may differ.

Before you hand in a sample

  1. Follow your laboratoryIts instructions come first. WHO guidance specifies two to seven days without ejaculation.
  2. Collect the whole sampleUse the approved container. Tell staff if any is lost, especially the first portion.
  3. Keep to the deadlineIf home collection is allowed, confirm the delivery time and transport conditions.
  4. Mention what has changedRecent fever, illness, new medicines or collection difficulties help the result be read fairly.
A summary of the steps in this section. Your laboratory’s own instructions take priority.

Use the container supplied or approved by the laboratory and aim to collect the entire sample. Tell staff if any is lost, especially the first portion, which can contain many sperm. Ordinary condoms and lubricants may affect the sample; ask the laboratory about suitable options if collection is difficult.

Watercolour still life of a closed specimen container with a teal lid, a clipboard form and a paper bag on a clinic counter
Use the container your laboratory supplies or approves, and follow its collection and delivery instructions.

If home collection is permitted, confirm the delivery deadline and transport conditions in advance. Record the collection time and abstinence interval. Mention recent fever, illness, medication changes and any collection difficulties so the result can be interpreted fairly. A high fever can lower sperm concentration by about a third for two to three months, so a test done soon after a fever may need repeating.

Semen measures naturally vary. If a result is abnormal, European guidance recommends at least two tests before drawing conclusions (a strong recommendation); if every value is within the reference values, the WHO suggests not repeating it. If no sperm or very few are found, the test is usually repeated as soon as possible, with specialist review. Guidelines differ on how long to wait before a repeat, as the box below shows. Your clinician should set the interval; do not delay assessment simply to finish a lifestyle programme.

The key ideaStrong evidence: A guideline recommendation rated Strong (European or US urology guidelines), or a high- or moderate-certainty systematic review or randomised trial, with the major guidelines agreeing.

If a semen test is abnormal, it should be repeated before any conclusion is drawn.

Read more: WHO laboratory manual for human semen, sixth edition (2021) · WHO guideline for the prevention, diagnosis and treatment of infertility (2025) · EAU guideline: Male infertility · NICE NG257: Fertility problems: assessment and treatment (2026) · South African National Department of Health: National clinical guidelines for safe conception and infertility (2020) · Carlsen et al. (2003): fever and semen quality · NHS: Low sperm count

03 · Sperm DNA test

Sperm DNA testing: when does extra information help?

Sperm DNA fragmentation describes breaks in the genetic material sperm carry. A routine semen analysis does not measure it directly, and a sperm’s appearance cannot tell you its DNA result.

Concept illustration of a sperm cell and an interrupted DNA ribbon
DNA fragmentation is a separate laboratory question. A sperm’s appearance cannot reveal its DNA result.

Several different tests exist, called TUNEL, SCSA, SCD and Comet. Each uses its own method and cut-off, often somewhere between 20% and 30%, so a “high” result from one laboratory cannot be compared directly with a result from another.

The major guidelines disagree about who should be tested, as the box below shows. None recommends the test for every man as part of a first assessment. Before testing, ask what decision would change with the result, and whether that change is supported by evidence on outcomes that matter to you, such as a live birth.

The key ideaModerate evidence: A guideline recommendation rated weak or conditional, or consistent results from reviews of observational studies, without major disagreement between guidelines.

A sperm DNA test is not part of a routine first assessment. It may be offered in selected situations, such as repeated miscarriage.

Read more: WHO laboratory manual for human semen, sixth edition (2021) · Santi et al. (2018): sperm DNA fragmentation cut-offs, a review · NICE NG257: Fertility problems: assessment and treatment (2026) · EAU guideline: Male infertility · AUA/ASRM Male Infertility guideline, amended 2024 · ESHRE good practice recommendations on add-ons in reproductive medicine (2023)

04 · DNA results

Sperm DNA: what the results can and can’t tell you

Kara’s research area: Kara designed research on how sperm DNA integrity changes as men get older. The findings below come from the largest published studies.

Higher levels of sperm DNA damage are consistently linked with poorer outcomes. In couples trying naturally, very high levels were linked with a lower chance of conceiving each month. In one large clinic study, results above 30% on one test were linked with lower IUI success. Across IVF studies, high DNA damage was linked with lower pregnancy rates, and less so with ICSI.

High DNA damage has been linked with about twice the risk of miscarriage in fertility-clinic studies, and men whose partners have had repeated miscarriages tend to have more DNA damage. Whether treating it prevents further losses is unknown.

But a link is not the same as a useful test. A review of how well these tests predict pregnancy after IVF or ICSI found them only “fair” at best, and two of the common tests were poor. The result also could not show whether IVF or ICSI would work better for a couple.

Some things are linked with more DNA damage: smoking, a varicocele, poorly controlled blood sugar, air pollution and being 50 or older. Stopping smoking is worthwhile for many reasons.

Steps that can lower DNA damage have not been shown to lead to more babies. Repairing a varicocele that can be felt on examination lowered DNA damage by about 7 percentage points on average, in studies without comparison groups. A one-day gap before a sample, rather than three days, made no clear difference to DNA damage or pregnancy rates in a small randomised trial of IUI. Antioxidants lowered DNA damage a little, by about 4 percentage points on average after three months in a 2025 review, but that has not been shown to lead to more babies, and the UK’s NICE advises against offering them for this.

Some clinics offer to use sperm taken directly from the testis when DNA damage is high, because testicular sperm tend to carry less damage. Early studies look promising, but there are no proper randomised trials, it involves surgery, and the guidelines disagree, as the box below shows.

The key ideaModerate evidence: A guideline recommendation rated weak or conditional, or consistent results from reviews of observational studies, without major disagreement between guidelines.

High sperm DNA damage is linked with lower pregnancy rates and more miscarriage, but today’s tests cannot predict what will happen for one couple.

Read more: Spanò et al. (2000): sperm chromatin damage and natural conception · Bungum et al. (2007): sperm DNA and IUI, IVF and ICSI outcomes · Simon et al. (2017): sperm DNA damage and IVF and ICSI, a review · Robinson et al. (2012): sperm DNA fragmentation and miscarriage, a review · McQueen et al. (2019): sperm DNA and recurrent pregnancy loss, a review · Cissen et al. (2016): how well sperm DNA tests predict pregnancy · Szabó et al. (2023): factors linked with sperm DNA damage, a review of 190 studies · Lira Neto et al. (2021): varicocele repair and sperm DNA, a review · Szabó et al. (2025): treatments that lower sperm DNA damage, a review of 86 studies · Kabukçu et al. (2021): abstinence time before IUI, a randomised trial · Esteves et al. (2017): testicular or ejaculated sperm for high DNA damage, a review · Khoo et al. (2024): testicular sperm for high DNA damage, an updated review · NICE NG257: Fertility problems: assessment and treatment (2026) · EAU guideline: Male infertility · AUA/ASRM Male Infertility guideline, amended 2024

Your questions

What you may be wondering

What if I lose some of the sample?

Tell the laboratory. An incomplete collection can affect interpretation. Follow the laboratory’s instructions rather than hiding a collection difficulty.

Should everyone have a sperm DNA test?

No major guideline recommends it for everyone. The UK’s NICE advises against it; European and US urologists suggest it in selected situations, such as repeated miscarriage. Ask what clinical decision a result would change.

Myth vs evidence

Common worries, explained carefully

Myth

“Low morphology means most sperm are dead.”

Evidence

Morphology describes shape. Vitality describes whether sperm are alive, and motility describes movement. These are separate measurements.

Myth

“One result tells us everything.”

Evidence

Collection, natural variation, illness and clinical history can affect interpretation. Your clinician may recommend another sample.

Myth

“A reference value is a pass-or-fail fertility score.”

Evidence

WHO lower reference values describe a reference population. They cannot determine an individual’s chance of pregnancy by themselves.

Myth

“Lowering sperm DNA damage is proven to lead to a baby.”

Evidence

Some steps lower DNA damage, but none has yet been shown in trials to increase live births.

Words you may hear

The terminology, translated

Concentration
The number of sperm per millilitre of semen.
Total sperm number
The number of sperm in the whole ejaculate.
Motility
How sperm move. Progressive motility describes forward movement.
Morphology
Sperm shape assessed against laboratory criteria.
Vitality
The proportion of sperm that are alive.
DNA fragmentation
Breaks in sperm DNA; not measured directly by routine semen analysis.
TUNEL, SCSA, SCD and Comet
Names of different sperm DNA tests. Each has its own method and cut-off.
Take to your appointmentYour appointment checklist
  1. What does the full pattern of results suggest?
  2. Was the sample complete, and were the collection instructions met?
  3. Should I repeat the test, and when?
  4. Would DNA testing change a decision in our circumstances?
  5. If a DNA test is suggested, which test and cut-off does the laboratory use?
Watch with Kara

Videos on this guide

Videos on these questions are coming to the channel:

  • What Is a Semen Analysis?
  • Understanding Sperm Count
  • Understanding Sperm Motility
  • Understanding Sperm Morphology

See the video schedule

Sources & further reading

Sources 26 studies and guidelines Show the research

Prepared using Kara’s research library and checked against the linked clinical and patient-education sources. The explanations and new diagrams are original educational adaptations.

Watercolour concept of small sperm cells approaching a large egg cell, framed by eucalyptus leaves (not to scale)
Concept illustration, not to scale.
Both partners

Fertility is a shared picture

For every couple, the health and results of both the man and the woman shape the plan. These Fertility Library topics sit alongside this guide.